Showing posts sorted by relevance for query lashawnna. Sort by date Show all posts
Showing posts sorted by relevance for query lashawnna. Sort by date Show all posts

Saturday, April 21, 2012

Internet Con Artists: A Cautionary Tale

This is the story, the stories, about a woman that I met on the Dr. Phil website, back when I thought a support group for chronic pain was a good idea.  (It sometimes was.) She goes by many names, but they're all similar.  She is a con artist and she persists, oozing beyond the tough talkin' Texan's website that was once her primary hunting ground.  She is rascally.  She has her own section in the North Carolina criminal data base, where the charges and the many dodges of the justice system that are apparent there give the strong impression that she has mad con skills.

Personally, I think she is dangerous.  I've absolutely no evidence that she has ever encroached on anyone's actual personal space.  She has not shown up at my door.  The last I heard from her, in fact, she said:


I don't want any further contact with you!!!!
Do I make myself clear!

I tend to have that effect on people, particularly those I meet through that big, bald entertainer, Phil McGraw.

Most of what follows has been published here before, but for some reason, maybe because it is ongoing, Shawnna's story always ends up as a draft. Well, it's a quiet, cloudy Saturday morning and I am determined to rid my inbox of as many unfinished pieces as possible. The several posts dedicated to Shawnna the Internet Con Artist just need a bit of unification, and some updates.

The most important update to "Shawnna's Con" is that she has switched monikers again.  Occasional name changes, usually due to some technical gaffe, are not unusual in our online lives, but someone who does it frequently needs to be viewed with skepticism.  Or, if you have one handy, a jaundiced eye.

One jaundiced eye, courtesy of
Ohio State Univ. College of Nursing


In a fit of major clever, Lashawnna Burney is going by Lashawnna Willamson-Smith (as well as Williamson-Smith).  For having made that swift play with the Letter I, she gets a sticker!  And a half-point for full-fledged trickery:  She likes to present the misspelled Willamson-Smith as a first name, because that is really gonna throw people off, eh wot?

So, anyway.   If you participate in any sort of self-help or support group on the interwebs, you will eventually meet your own Lashy Shawnna Shawna Lashawnna Lashawna Lashonda Burney Willamson Williamson Smith Smythe.  I am sure there are other incarnations, as well, suitable for other cons.

Please don't be incredulous.  Rather, laugh at my discomfiture, sure!  But be vigilant, as well, protect your personal information, and consider referring your virtual friends to organizational help in the event of Big Troubles, in lieu of, for example, writing them a check.  The bad apples in the big internet pile of fruit are few but they're everywhere, they're talented, and most likely sociopaths.  You cannot convince them to come clean or go straight.  You cannot elicit an apology or make them feel guilty.  If you offer any sort of gift, material or immaterial, make sure it is something you give freely, with no strings attached, no expectation of acknowledgement or change in behavior.  It just won't happen.

Shawnna seems to enjoy reeling people in on her fishy lines of drama and trauma. She invades your heart, heartlessly, and does it in such volume, with such volubility, that she can make you forget what you know.  One of her more mundane arrests came on the same day she claimed a fabulous thrust-and-parry with Death -- an Easter Sunday.  Even knowing this, she grabs my attention when she writes that, in her version of the Resurrection Day, "they had to Life Flight me..."

Resurrection Jealousy.

I may as well confess, not for the first time here, that I am the World's Easiest Mark. It is great sport among my family and friends to see just how much junk they can get me to believe. I melt at a low temperature, cooing "Oh no, really?" upon hearing their sad, implausible sagas.

But I think I am wising up! At least with Fred. He has some "tells" that I can now identify, chief among which is the statement: "This is a true story." But, oh, how it delights him when he, too, can reel me in.

My former best friend in the whole wide world is a Gorgeous Iranian Lesbian. We met as undergrads, roomed together for a while, and -- even though I screwed up our relationship in recent years -- had a wonderful life together. She just could not believe the extent of my gullibility. One day, we were working on homework in the French Dept. lounge, trying to come up with paper topics for our 17th century literature class. She hit on something she thought I would like -- having to do with that famous classicist Oussama Mon Chénier.

The Shah-Meister regaled me with fond memories of her relationship with this naturalist of the Grand Siècle, and how she spent many a rainy afternoon stretched out on her bed in Téhéran, thumbing through his great and marvelously illustrated work:  L'Histoire Naturelle des Animaux Sauvages (The Natural History of Wild Animals).  She had never understood why it was such a beloved reference work in Persia but rarely known among Unenlightened Westerners.

By the time she convinced me to go and interrogate our Professor Aronson là-dessus, I was frothing at the mouth at the thought of the academic wealth awaiting my investigation.  I will just let you imagine my horror at the kindly sad smile which my respected professor assumed about 10 seconds into my presentation of this awesome paper topic... Truly une idée "reçue."

And then there was the Incident on the Berkeley Pier.

But "Shawnna"?  She's on a whole other level, tending toward malevolence, not the gentle joshing of friends.

Here is her tale, updated from the original version, published here in January 2009.  Though I'm able to piece more of the puzzle bits together, I've not gained many insights into her behavior.

****************************************





It's beyond disconcerting: beyond it, though, to I don't exactly know what.

The popular initial reaction seems to be "disappointment." That surely was the killer reaction that worked best on me as a child -- nothing hurt so much as when a beloved adult would calmly (with maybe a Touch of Glum) express disappointment in me and in whatever behavior I had perpetrated.

For 18 months, this woman Shawnna interacted almost daily with me and several other people in an online group that dealt with living with chronic pain.

There is another woman in this group who keeps me sane. Her latest daily adventures include stealth feeding of her neighbors' horses -- or, in one of the instances, the girlfriend of a neighbor who is billeting her horses there for the duration of the love affair. My friend is an animal lover.  These horses were not being fed daily and did not have access to fresh water -- and she has reacted as most of us would. Well, not quite. I would be on the phone reporting them, neighbors or not, for the talking-it-over approach has obviously been tried several times.  I do not, apparently, understand the dynamics of life in rural Wyoming, as such an act might well, she tells me, push her neighbors over sanity's edge... and then what would she do?  It'd be a shootout and it'd be all my fault.

So, she does the only logical thing:  She and her 80-something mother take hay to the two separate pens. I don't know the story of the other neighbor. They wait for the cover of darkness and deliver hay and water. The horses apparently go ape shit every time they see either of the two women, or even their truck.

She has a good heart.

So I am going to go way past "disappointment" and charge on down the path all the way to ANGER. Not at this caring Wyoming gal, no!

At the woman who has fooled her, and me, and lord knows how many others. We nicknamed her Shawnna. She was thrilled when she was given a nickname. It made her "one of us," one of the gang, party to the inner circle, whatever -- it marked the moment when she had definitively snookered us all.

I spent part of the day digging up every post she had ever published at the web site that hosted our laughter-loving chronic pain support group. Somehow, she never expected anyone to piece all the disparate parts together. Well, I got right to it, didn't I? It just took me a year and a half.

This is the story she has written, in bits and pieces, some meant for one group, some for another:

She is in her late 40s. She recently lost the triplets she was carrying -- made it to 6+ months, though. There are several posts about her inability to go into the nursery and pack up the tiny clothes and take down the cribs, maybe throw a little paint on the walls, scrape those silly stencils off, try to sell that stupid rocking chair on eBay.

That was mostly for Phil McGraw's online grief support group that rallied around her as she faced the anniversary of the triplets' death, and with whom she went on to share her childhood experiences of incest. Eventually, I guess, there was a strong sense of incongruity, and she moved on to the more appropriate Childhood Sexual Abuse Survivors Group, never speaking of the dead babies again.

About that same time, she approached us, the Chronic Paineurs, with a need for advice about having, or not having, a hysterectomy. The reason given was "pelvic pain." For reasons that I could never figure out, her surgery was supposed to take between 6-8 hours and might result in her death, or a colostomy. (Tonight, I relish that symmetry: her death or a colostomy. I like those odds.) She said she'd had 15 previous abdominal surgeries.

Let's see... She suffered from cardiomyopathy and a well-controlled seizure disorder, although she had a seizure on the operating table during her last operation and... you got it! Almost died.

"I almost died" could have been the chapter heading for most of her revelations.

She had three adult children. Her son was in prison for murder. Oh. As it happens, her brother was going on trial as a serial killer, and she lived in dread of having to testify. Her oldest daughter was a heroin addict with two small children. She popped into the narrative as a regular character when Shawnna decided she should have AIDS, abandon her kids (the long suffering Shawnna and her husband Rudy dedicated themselves to raising them, of course), and run off to New York with a no good man.

Shawnna's youngest daughter was a straight-A student, finishing her first year at college, and had never caused, or been in, any sort of trouble, ever. With the now added burden of two toddlers to raise, we suggested to Shawnna that her "good" daughter might be able to help out on the weekends. "Oh no," we were told, she did not want to be a burden to this young one who was doing so well.

Not even after her surgery went awry and she was mostly bedridden and living on methadone and percocet (Hey! I resemble that remark!) would she consider asking her daughter for help. She would carry on, somehow -- taking care of those two grandchildren, volunteering at their schools, working at the funeral parlor (part-time) and taking care of what she called her "wifely duties" with Rudy. [Prior to working at the funeral parlor, Shawnna said she owned a Home Health Agency, which she loved, as it allowed her to use her training as a *nurse*! I guess that is not an altogether uncommon move, to go from the healing arts to the death business?]

Of course Shawnna's surgery did not go well! This was surprising, as it took place at UNC-Chapel Hill (those slouches!). Would you believe that the numb nuts left a sponge inside of her? She ended up needing more surgeries because of their horrid oversight.

Then began the Saga of the Vaginal Bleeding. I know that it stretches the bounds of your credulity, but it was only at this point that she lost me as one of her dedicated cheerleaders. Because she kept bleeding and bleeding, going in and out of the hospital several times a week. I have also had a total hysterectomy and my crude understanding of anatomy informed me that there just are not that many sources for such bleeding... Somehow, I assuaged my suspicions with the reassurance that I apparently did not know everything, and that Shawnna was surely cursed and being used by God to do a rewrite of the Book of Job.

(Book, shmook! I forgot to mention that she is an author of two books. No, I haven't been able to find either one.)

Oh, I grow weary.

Well, what is left to Shawnna's Tale? Ah, yes. Rudy almost passed away about 2 years ago -- he had a major stroke at the age of 33. A few months later, he up and died -- he was out mowing the lawn and had a massive heart attack.

My tenderhearted Wyoming friend prepared herself for service -- a plane ticket, her own home and hearth in order -- and waited for details. Waited and waited. Shawnna was impossible to reach.

Suddenly, she posted a message saying that she was going to relocate to Memphis, Tennessee. I had begun searching for a death notice, checking obituaries in her area, then anywhere, then under any mistaken spelling of the poor dead man's last name. Nothing, nada, zilch. I asked her about it, finally, and was told that her world was turned upside down (understandable, nod nod...) and that Rudy's adult son from a previous marriage was handling those details.

Okie-dokie, then!

After a bit, she reappeared, reintroducing herself this way in an email, afraid, it seems, that the various plots of her story might have become stale:


I know that it's been a very long time, I'm fine. I have 4 grandchildren now, and all by the same daughter. I have three of them. I had a stroke on this past Easter Sunday but I must say that with some physical, and speech therapy I'm doing much better, I have been missing both you and M but I almost lost my  mind girl after my husband passed away. I'm much better know, and I've learned to cope with it. I love you just the same as I did one year ago girl!

Love,
Lashy

Finally, a period of relative calm, with only occasional hospitalizations for congestive heart failure interrupting. She was off to her new life in Elvis Land.

Except that we heard nothing and could not reach her. Finally, we received a message that she had suffered a major heart attack while driving...

With a familiarity that suddenly *was* breeding a major pile of contempt, we could not contact her at the hospital she was supposedly at and so on and so on and so forth.  In the past, her "good daughter" would appear online at these times of crisis, and promise to relay messages, etc.  There appeared to even actually be such a daughter that my friends were able to reach by phone.  Something in that precious mother-daughter relationship became irrevocably strained at this point, however, because Lashy wrote, out of the peculiar blue:

She  is  doing well, she is studying at The University of Winston-Salem now. She is in her 5th year of schooling. She is still studyimg to become a Psychologist. But guess what? She doesn't even call me, come to see me. She didn't even come to the hospital after I had the stroke, and I had been life-flighted there to Winston-Salem!!!!! I was sooooo hurt. I just couldn't believe that she didn't come to see me. I haven't heard from her now in almost a year. I just this information from her father. But  I am not going to sit and worry about what is going on, I love her, have done not one thing for her to treat me the way she's been, and one day she'll regret the time that we didn't share together.

There is, of course, no University of Winston-Salem, so I assumed it a reference to Winston-Salem State University.  But it, of course, has no graduate program in psychology, but does have a good-looking undergraduate BA degree in the field.

It was a great set up.  Now Good-Daughter-Turned-Mean-Child could not be relied upon as a benevolent player in Shawnna Land.  You can't trust her or believe a word she says!  Curses, though, that the little demon spawn now has training in psychology and will trick us all with her wily ways!

That fix was apparently not enough, however, because Shawnna went on to have Good-Daughter-Turned-Mean-Child suffer a stroke, herself, and be put, herself, on the "transplant list." Again, Lashy was kind enough to provide all sorts of contradictory written information, though she never seems to completely hoist her own petard.  This is a letter she sent to my good friend during Scene 4 of Act 3, or whatever we are to call this internet con drama.  It's one of her more elaborate, and the construction is interesting, particularly the opening gambit.  Hi, it's been forever, my dying-with-AIDS daughter is such a whore... my Good-Gone-Bad-Now-Redeemed-Again daughter is in ICU... all summed up by the telling, "Oh my God girl!!!! What more can I deal with huh?"  It's all about Shawnna.


I don't know the requirements for receiving hospice care, but apparently they are not as stringent as I believed!


----- Original Message -----

Hey Girlie,
I know that it's been a while that we've spoken. How has everything been going for you? I have some very disturbing news. I just found out very recently that my last granddaughter is not my daughter's husband's daughter!!! No, her father is some other low-life piece of shit that roams the city of Fayetteville! The DNA test just came back last week. I am so through with my daughter do you hear me! So now we've got to try and find this someone to let him know that he is now a Father. I spoke with my daughter and asked her what the hell is she thinking? Not only were you unfaithful in your marriage but you had unprotected sex with someone that you really don't even know!!!! She tells me that she's been knowing this man for a year! Uh....wow...a whole year!. Please, give me a break!

Plus the fact that T (my youngest daughter) is in ICU and has been for the last past four days, we found out that she has inherited my cardiac condition. She has an enlarged heart and went out to the emergency after feeling very ill. She was having difficulties breathing and was having some swelling in her legs and hands. Oh my God girl!!!! What more can I deal with huh? But the good news is that she's doing better and the Physician told me that he'd be able to step her down off of the milirinone lactate and put her on an oral medication at this point. So hopefully she's be discharged at some point this coming week. 

I always feared one of my three children inheriting my cardiac condition and the one that has her shit together is the one that has been crippled with this enormous problem. I'm very afraid that this will limit her ability to have children one day when she's ready. All I can do is guide her and show her how to deal with this cardiac problem. They have put in a picc line so that she can be administered the milirinone, the same medication that I use on a continuous basis here at home. My picc line has been sewn in place though.

**[Lashy simultaneously posted elsewhere that Good Daughter Gone Bad was comatose, had had a stroke and suffered severe neurological deficits.  Milirinone (sic) lactate?!  Yowza!  In the little bit of reading I did about the drug, one thing was pretty doggone clear:  "treatment with this drug usually does not exceed 5 days..."  This archived drug label made it clear that this warning against longterm use was not lightly made:

Whether given orally or by continuous or intermittent intravenous infusion, milrinone has not been shown to be safe or effective in the longer (greater than 48 hours) treatment of patients with heart failure. In a multicenter trial of 1088 patients with Class III and IV heart failure, long-term oral treatment with milrinone was associated with no improvement in symptoms and an increased risk of hospitalization and death. In this study, patients with Class IV symptoms appeared to be at particular risk of life-threatening cardiovascular reactions. There is no evidence that milrinone given by long-term continuous or intermittent infusion does not carry a similar risk.]**


I was in the hospital for my birthday, (7th January). I was in CHF and renal failure. I am better now and hopefully I won't have another hospitalization for some time.

I allowed my daughter to come over to spend a few hours with all of the children during the holiday and she didn't even think or consider buying either child anything for the holiday! I was very disappointed in that too. I have just come to realize that my daughter will always be selfish, bottom line. 
Have you talked with M lately? I would like to go and see her for my 1-week vacation this coming April once the kids are out for Spring-break but I haven't heard back from her to confirm. I would like to come see you one Spring/Summer as well.

I really miss you guys so much. I feel so bad sometimes girl that it takes all I have just to get up and move around each day. My cardiac health is slowly declining, and I can really feel the change. I have hospice coming in each day and they've helped me aloft as far pain relief, and making dr's appt's for me.  And I have a CNA to come out each day for three hours. She helps with laundry and running errands for me.
I just wish that I could feel 30% better. [This is, I think, my new Lashy/Shawnna favorite.  In my mind, I hear it à la languishing Scarlet O'Hara:  "I just wish that I could feel 30% better..."]

I had a difficult time yet again this year during the holidays because as you remember Rudy passed on the 6th December. I must admit that having friends and family here for the holidays did distract from the depression that I was feeling but, It was still difficult and I guess that it will never really go away. 
Well Sweetheart, I've taken up enough of your time with my whining so I just want to let you know that truly I love you very much and because I may not post or send messages as often as I did before, doesn't mean that you're not on my mind. I look forward in hearing from you soon....Talk later 
Love,
Lashy
P.S Have you heard from Prof? If so, please give her my hello's.......................
[Prof, here, chuckling...]

Somewhere in all the chaos, Lashawnna began to mention LVADs, though it was never clear whether she had one.  It became something of an obsession.  Still -- as you might expect -- the LVAD stories came with their own healthy quantity of red flags.  Small flags, maybe more of a bled pink than a screaming ninny of a cerise.  Things like continued smoking, something that I'd think one might give up if faced with left ventricular failure.

I was contacted by a very nice guy who is an authority on LVADs and whose blog is dedicated to helping others learn about the life-saving devices.  Shawnna was driving him a bit mad, writing, then calling him repeatedly with requests that he call her, and performing her typical zero-to-sixty insistence on intimacy and instant friendship.  She glosses over the normal periods of making acquaintances so as to rapidly insert herself and her confusions into the mark's life.  Unfortunately, she just came off sounding weird to him and he did an internet search... finding, eventually, my previous post, "Shawnna's Con."

An aside:  What a wonderful guy, what a wonderful attitude!  He is steeped in gratitude, and it shows -- well beyond words, it shows in pictures and videos, it shows in how he reaches out to give others a hand up.

My capacity for playing the fool has amazed me. I still want the thousand dollars back that I gave to someone I "met" online in an osteonecrosis support group.  I did not hesitate to help her pay her electric bill so that the utility could be turned back on, keeping her young children warm. One of her sons was very ill, she said, and she couldn't afford to take him to the doctor.  Are you sitting down?  Turns out she had other uses in mind for my money, uses that were more in the line of "entertainment."  Well, we are all deserving of fun... Right?

I still wonder whether I had any right to expect my osteonecrotic friend to use those bucks for her overdue bills. Did I have any right to know what she used the money for, at all?  The answer is clearly "no." But the emotional truth is something different.  And ugly.

I never gave Shawnna anything material.

No, I cried with her, listened, tried to help and advise, pitied and prayed for her -- and for "hers," who were always so deep into trouble, lost without her able help and guidance.

I cannot even laugh at myself as I begin to seriously fret over who is taking care of those beautiful, innocent grandkids.  Even after all of this, I believe in the existence of those children, mostly believe the stories that accompany them, and fear for their welfare.

Because I cannot know what tidbits are true, which are false, which are more properly interpretations.  She may have a failed heart, her daughters might be equally ill -- one sticken with Lashy's own disease, an inheritance, the other with AIDS, Lashy's emblem for "bad."

The proliferation of grandchildren, all born to an HIV+ woman, is at the heart of this con's tale.  Babies, some of them dead (her opening at Dr. Phil's, remember, was that she had just lost triplets), all of them displaced, are what's the matter.

I wish I understood.

It turns out that Shawnna may have an online accomplice. So I -- and others, especially one kind spirit in Wyoming -- are waiting for the other shoe to drop in the saga of Shawnna's con.  She wants to set a trap, and has, probably.  I just want to issue a Public Safety Announcement -- which is what I suppose this post was supposed to be.

But oh, Dear Readers, there was one wondrous development, just a few months ago, and I will end this rambling "cautionary tale" by copying below a rare moment of love and warmth between myself and this con artist.

You can imagine how thrilled I was to be able to notify Shawnna, in January 2012, that there had been a resurrection, good news of the miraculous sort:

lashawnna wrote: 
"Morgan and Dianah I know that it's been a while since I last spoke to either of you, I have been really having a hard time dealing with the death of my husband, so much so that I had to relocate to another home, too many memories.[...] Prof, I have really had you in my thoughts and prayers and I hope that all is well with you. I have had to really dig deep for my sanity, for a time there, the walls started to close in on me and I felt as if I was losing sight on reality. I couldn't sleep because I was in constant thought of Rudy. I have lost 39 pounds. When I first started posting, I wore a size 14 pants, now I am wearing a size 5/6."

i, profderien, wrote: 
hi lashy,
long time, girl, long time!
but i am so glad to be able to come to you with good news.  
heck, it's great news!  
are you sitting down?  no?  well, take a second and sit yourself down, because i don't want you to faint and hit your head, thereby sustaining a life-threatening subarachnoid hemorrhage or possibly fracturing the medial epicondyle of your humerus (the "funny bone"!).  heck, the joyful shock of what i am about to disclose to you, our dear loving lashy, might cause your cardiac muscle to shift into overdrive.
it's PHENOMENAL news!  it's put-it-on-the-doctor-phil-show-it's-so-good news!  (seriously, my friend, you would make a fascinating guest.)
ready?  are you sure?  okay, here goes:
RUDY IS ALIVE AND WELL AND WORKING AT WALMART!  it's a freaking miracle.
no, i am not pulling your tiny size 5/6 leg!  it's time to have a really big, fattening meal in celebration -- but cardiac-friendly, of course, maybe an arugula salad dressed with balsamic vinaigrette, some poached salmon over a lovely parsnip purée. (i'm hungry.)
you probably don't believe me, i know what a stickler you are for truth, justice, and the american way -- and here i am, saying rudy (by whose grave you wept and loss scads of weight) -- that scumbag who pretended to stroke out while mowing the lawn -- here i am saying that your husband rudy is flaunting his status as a living organism... all over facebook!
i wasn't sure, and again, out of respect for your reliance on honesty, i asked someone who knows what rudy looks like to take a gander at his profile picture.  i was assured that "yep, that's him!  the no-good pretending-to-be-dead bozo!" 
i know, this news is really a mixed bag.  part pure relief (He Lives!) and part ultimate frustration (How Could He Let Me Grieve and Waste Away to a Size 5/6?).
but you are nothing if not a strong woman, accustomed to adversity (good lord, when i think of the tragedies your family has suffered... the loss of your triplets, your brother's murder conviction, your son's murder conviction, your daughter's HIV, your other daughter's cardiomyopathy, your own cardiomyopathy, your multiple and simultaneous needs for a heart transplant... why, it boggles the mind, if not one's credulity!).
i gotta say, though, lashy... i believe i would divorce the bastard.  no doubt you have moved on in these intervening years, and some other lucky man has scooped you up.
well, that's about all.  i hope you can get over the shock of it.  this is a great place to vent, though, you know? everyone here is like FAMILY, gullible as all get out, willing to lend you sympathy, understanding, love, and probably a ten spot or two.  you can say *anything* here.  it's a safe place, where no one trolls for victims to exploit, where no one even considers playing a con.
all the best,
prof




Saturday, February 2, 2013

Jackie and Mel: Think of the Things You Can't Remember


On 24 January 2013, over at Phil McGraw's half-dead blog, Turning Point, a viewer wrote in wondering where she might find a place to discuss chronic pain issues on his website.  The Chronic Pain Message Board used to be my morning cyber café spot, where I'd have my first few shots of the day with good friends sharing similar circumstances.  Granted, when there were no fires to put out, we mostly chatted and gossiped and braced ourselves for the coming day with bad jokes, more chat, and wisecracks at the expense of spouses, caretakers, children, pets, and, occasionally, Phil Himself.

No one answered her, so I did, on the 31st.  There is no more Chronic Pain Message Board community.  Whether that's good or bad, I can't say.  I maintain four friendships, of diverse type and degree, from that wild coffee klatch bunch, and keep track of two others.  There's one woman from the old board, though, for whom we maintain several food-rigged traps, on either side of the approach to the drawbridge, even one on the inside ring of the moat.  The carnies and Cirque du Soleil addicts in recovery, who lodge in the barn during most of their detox and rehab, keep an eye out for her.  Which just proves that every online support group has its share of potentially dangerous weirdos.  Recent rumors have Lashawnna as deceased, but I'll believe it when I pry her wireless mouse out of those cold, dead, con artist hands.

Um, yeah.  So this very nice woman imploring Dr. Phil to explain the realities and needs of people with Chronic Pain ended up just getting me, an anti-McGraw fanatic, recommending that she give the insanely cheerful Depression Group a go, since depression and pain go hand and hand, go round and round.  I'm sure that wasn't terribly helpful.  Everyone really just wants to hear the sexy deep tones of that near tennis pro, Phillip Calvin McGraw.  Here's a recent photo of the man warning everyone to keep their eyes on the ball in the back of the turnip truck while they flip those four-dimensional Texas corncakes -- after he evidently got distracted up at the net:

Courtesy of the DrPhil Twitter Feed

And I renew my oft-noted characterization of Bubba McGraw as a metrosexual.  Look at those finely plucked brows.  Maybe the Chronic Paineur looking for help also saw it, and got a chuckle, released a few endorphins, and felt a bit better.

Writing that brief response on his blog made me nostalgic for those good old days, when I had coffee with Ms. Diana-With-An-H and checked in with Ms. Carol.  So I went digging for some archival memories.  But the very first page I turned up had me remembering things a bit differently.

It is people who either have no resources or who don't know how to use them... It is people who have no medical options and begin to lose touch with reality, hoping for a chubby Texan celebrity talk show host (known to believe that most everything somatic is caused by heavy metal toxicity) to come loping along on a worn out swaybacked white stallion to save them -- for free... It is people like myself who are desperate for any kind of relief, no matter how ridiculous... that make up the demographic of vapid online support groups.

But buried in there, as frequently as on every other page of archival material, were plaintive calls for help from folks usually never heard from again.

What happened to Jackie, whose Mother typed her entry for her, as she could not?
And Mel, who wrote her very first post as an answer to Jackie, where is she now?

As someone I once knew often urged me:  "Think of the things you can't remember."

Without too much further ado [!], here are Jackie and Mel's post from McGraw's former Chronic Pain Message Board, both posted on 5 September 2005.  Jackie, like so many people who manage only to post once -- that once taking a lot out of them -- thought she was writing directly to "Dr. Phil."

I've tried to eliminate/change any identifying details, like last names, ages, regions -- but nothing can erase the pathos, and the knowledge that there are thousands upon thousands of other Jackies and Mels, who feel as if they've nowhere to go, and that no one is listening.

NOTE:  Jackie refers to Dr. H and his clinic (obviously not in Nicaragua, but that's all I could come up with!), plus his infernal website, and I'm sorry to say that Dr. H turned out to be a hoax, even doing prison time for Medicaid/Medicare fraud.  But this is how precious hope is kept alive -- and cruelly toyed with -- for many people with difficult diseases.

JACKIE
September 5, 2005 4:27 pm EDT

Complex Regional Pain Syndrome (CRPS)
Hi. My name is Jackie V. At the time, I was 18 years old and had just bought my first car. I had a boyfriend who loved me and lots of great friends. I had a great job that I was really good at and paid well, and I had pride, dignity, confidence and humility. I guess you could say that I was just a normal girl, but there was nothing normal about how my life was about to drastically change forever!  
I had been waitressing and hostessing at a nice restaurant for months where on May 4, 2002, I had a minor injury. The doctor said I had hundreds of tiny shards of glass in the palm of my right hand (the hand that I write with). He said not to worry, that everything would be fine. But it wasn’t! Suddenly 1 week later, I had excruciating pain and extreme swelling and discoloration throughout my hand and wrist all the way up to my right elbow. I could barely even move my wrist or fingers without crying out in pain!  
When Workers Compensation Board got involved, right from the start they didn’t believe that all the pain and swelling was from the accident at work. So, I was passed from doctor to doctor to doctor, as each one would give up on me – not knowing what else to do. Most of them resorted to pumping me full of drugs and at one point, I was taking some medications because of the side effects of other medications. Honestly, I have probably taken more medications than about 20 people would take in their entire lifetime (and it’s only been about 29 months so far)!  
So finally, the diagnosis – for awhile it was Carpel Tunnel Syndrome, then it was Severe Tendonitis, then Reflex Sympathetic Dystrophy (RSD), then Fibromyalgia, hours later it was RSD with secondary Fibromyalgia, THEN it was all in my head and the latest diagnosis is Complex Regional Pain Syndrome (CRPS), which is the exact same thing as RSD. You know, my doctors spent so many months trying to figure out what was wrong with me, what it was called. And it got to a point where I really didn’t give a flying crap (sorry) what my disease is called, all I want is for someone to make it go away!!!  
(I wanted to give you a bit of info on CRPS so that you had some sort of idea of what I’m dealing with.)  
Complex Regional Pain Syndrome is a progressive disease of the Sympathetic Nervous System, an abnormal sympathetic reflex. It can follow a minor trauma (like a fall or sprain), a break or fracture, a sharp force injury (like a knife or bullet wound), heart problems, infections, surgery, spinal injuries or disorders or other major traumas. CRPS is a devastating, disabling disease that has completely robbed me of my ability to function because of extreme, severe pain that is constant and never-ending. There has not been even one tiny moment in the last 29 months when I have not been in terribly horrible pain! If it is caught, and most importantly correctly treated early, then most CRPS patients respond well to treatment. But in my case (and like so many others) it wasn’t, so I was left to try and cope with horrendous pain, impaired motor functions, body tremors, dystonia, full body muscle spasms, sympathetic nervous system dysfunction, extreme swelling, skin color changes, skin rashes, fevers, increased inner body temperature, sores, sensory changes, hypersensitivity, short-term memory problems, emotional distress, frequent migraines, daily headaches, insomnia and bone loss. So sadly, (believe it or not), ALL of these symptoms have become a part of my daily life! CRPS also causes depression, NOT the other way around like most doctors like to think!!!  
Ultimately, severe and disabling pain is the hallmark of this frustrating disease. Although countless doctors in Canada disagree, another hallmark of this disease is its ability to spread from one affected area, to another area, or in some cases, like mine, from one affected area through the entire body. As a result, few patients, like me, have total body CRPS and are severely incapacitated, in fact, the Mayo clinic has found that only 4% of patients get total body CRPS. I can’t walk, I can’t wheel myself in my wheelchair (because my right hand doesn’t work – I can’t move my fingers or wrist), so if no one is home and I have to go to the bathroom, then I have to crawl. I have to crawl on my stomach from the TV room to the bathroom and back. So, when it comes to be this late in the course of this disease, treatments are rarely effective and people like me are forced to cope with intense chronic pain!  
One thing that really bothers me is the fact that there is a huge lack of knowledge about CRPS, even among medical specialists. In fact, CRPS isn’t even taught in Canadian medical schools, so some doctors really believe that CRPS does not even exist! I believe it is only through the right education that we can stop improper diagnosis and treatments. I desperately need to make the public aware of this unbearably painful and crippling disease because it affects millions and millions of people throughout the entire world! It’s actually most common in people 40 to 60 years old, but recently doctors have found that it is now affecting people who are younger and younger (even as young as 3 years old).  
I guess the most devastating aspect of this illness is how it affects every single part of my life. At the very beginning of this letter, I mentioned some important things that I had before my accident, and now because of this stupid disease, ALL those things are gone and the scary thing is, is that I may never get those things back again! The really frustrating part is that physicians, other health care professionals, Workers Compensation Board workers, employers and especially friends, lovers and family members simply don’t understand just how much I am really suffering. They just don’t understand, they don’t get that I am in pain ALL day, EVERY SINGLE day.  
Not only is my disease extremely difficult to live and try to cope with every day, but I also have to deal with the many side effects of all of the medications I need to take (like weight gain – I was 115 pounds before my injury, and now I’m 257 pounds, also there’s dizziness, extreme nausea, major constipation, blurred vision, loss of appetite, hallucinations, completely passing out, even more insomnia and dopiness). As a result of all this crap (sorry again), I live, pretty much, without hope, in depression, anxiety, anger and fear! Pain, depression, being reduced to living in a wheelchair, not being able to dress or bathe myself and basically not being able to do anything a normal 22 year old should be able to do for herself results in even more anger, fear and anxiety. Complex Regional Pain Syndrome may not be physically fatal (like cancer or MS) and to you this might sound weird, but CRPS is definitely emotionally, mentally and spiritually deadly!  
Anyways there are 2 very important reasons why I wrote you this letter. First, I truly believe that we really need to educate our doctors (especially in Canada) about Complex Regional Pain Syndrome (most importantly, we need our doctors to be more open-minded and willing to learn), and I think it starts with making the public aware, letting everyone know about CRPS (knowledge is power, right!). This illness, that is just as debilitating and (in different ways) devastating as cancer, is barely even known about throughout almost all Canadians, let alone Canadian medical professionals! As a result, so many CRPS patients are misdiagnosed and mistreated for years and years! You know, the year is 2004 and this disease was around throughout both World Wars and STILL hardly anyone even knows this illness exists, let alone what it’s about, except for maybe, at the most, a handful of doctors. But the point is that there is no cure for CRPS! And if you think about it, most doctors don’t even know about Complex Regional Pain Syndrome, so they’re not even beginning to look for a cure! Maybe it’s because CRPS isn’t fatal like cancer, but honestly, from my heart, in May 2004 my grandmother died from cancer (colon cancer) and I wish to God that it could have been me!!! For the last year I have been praying to God that I had cancer, because if I had cancer then that would mean that I would get to die. It means that there would be an END, an end to all of my suffering and all my pain. When the pain is at its worst (and that’s pretty much all of the time, in fact the MaGill University’s pain index states that CRPS is the highest form of pain there is) I beg God to take me up to heaven. I tell Him that I can’t do it anymore, that the pain is just too much and I’m so tired of fighting, please take me up to heaven with You! Now you’re probably thinking I’m some suicidal lunatic, but I’m not and (unfortunately) I love my mother way too much to do that sort of thing. Studies have shown that 50% of people with CRPS attempt suicide.  
The other reason I wrote you this letter is because there actually is a tiny ray of hope for me. His name is Dr. H and he has a clinic in Nicaragua devoted to treating people with Complex Regional Pain Syndrome. And the amazing thing is that he is getting amazing results! He has not found a cure, but he is able to (in a great number of cases) reduce pain and increase mobility. Basically he’s able to give people their lives back! Also, Dr. H has even been able to put some of his patients into REMISSION where a patient’s pain is somewhere in between tolerable and non-existent! Some patients can stay in remission for years and years, but it would take barely nothing at all (like a sprain or a fall) and then BOOM, it all can be taken away! All the pain, headaches, spasms, hypersensitivity, swelling and insomnia are back and you can barely even move. You’re back in hell again! I don’t know about you, but I would definitely rather spend even just 1 week in remission with tolerable pain and have it all taken away, than being where I am today, in constant pain! Dr. H is doing excellent, amazing work with CRPS and it sounds like the doctors in Nicaragua know more about CRPS as well but we still need much more education! We desperately need to educate our Canadian doctors (most of them really don’t have a clue!) and it needs to start happening NOW! Basically, we need HELP! ALL CRPS patients need help. I desperately need help!!!  
The truth is that I really need to get to that clinic! Seriously, I think it’s my only chance at having some sort of normal, happy life! And of course, the only thing stopping me is money. For 1 treatment at Dr. H’s clinic, it costs $12,000 and you’re supposed to go every 6 months (but the price gets lower each time you go), plus the price of the plane rides there and back, and because I can’t take care of myself, my mother would have to come with me, as well, one treatment lasts a week and you can’t stay at the clinic, so my mother and I would need a place to stay during my treatment. It just all seems so overwhelming and impossible and we just don’t have anything anywhere near what that would cost! My mother is a single parent (still supporting her 2 young adults) and was just laid off a couple of months ago and (so far) hasn’t been successful at finding a job yet, so she’s been trying to make sure we have enough money to survive on for the next few months, so finding the kind of money needed for even 1 treatment is definitely IMPOSSIBLE for us! I know I’ve said it 100 times but I really do need your help! I just turned 22 (I’m supposed to have a place of my own, be working, studying for school and hanging out with friends) and now, to make matters worse, I’ve been informed that if we’re (my mom and I) not able to take “proper” care of myself with the help I have now (1 home care worker, for 2 hours, from Monday to Friday) then I will be forced into an institution. And believe me when I tell you this, I’ll die before I go to a place like that! My family, most of all my mother is the reason why I’m still here, why I’m still fighting this thing, why I’m still sane and if they were taken away from me, I really don’t know what I would do or how I would cope!!! Honestly, my mother is my best friend! She has been so strong and so supportive throughout all of this, and even though she knows that I might have CRPS the rest of my life (as bad as it is now), whenever I cry or the pain is really bad or it’s Tuesday, my mother always tells me “We’ll get through this together, we’ll get through this together!“ I desperately need her and my brother in my immediate space for as long as humanly possible so, that clinic in Nicaragua is my only hope! I’m desperate for help! Seriously, I need to find a way to get to that clinic or else 2 things will most likely happen:  
1. I’ll get even worse and have to be put into an institution.  
OR  
2. I’ll spend the rest of my life in immobilizing, excruciating pain, not being able to do anything for myself and praying every day for God to take me to heaven.   
Damn that’s depressing!  
  
Well, I realize this has been an extremely long letter and I wanted you to know just how much I really appreciate you reading this! For someone like you to take the time out of your busy day just to read my letter, it really means a lot to me and I can’t thank you enough! I want to make sure that you know that I wrote this letter because I want people to know what Complex Regional Pain Syndrome is so that hopefully one day even 1 person is in less pain (or NO pain) because a doctor happened to be watching TV or heard something from a friend and learned something. That would be SO amazing – even if this letter helped only 1 person! That’s why I wrote this letter, so that I might get the chance (the honor) to help others! If there’s anything you could do to help me, I would be forever (and ever and ever...) grateful, and I must say again THANK YOU for taking the time for me and my letter!!  
From: Desperate for help  
Jackie V  
   
P.S. For more information on Complex Regional Pain Syndrome you can go to www.--------
(This is Dr. H’s web site packed with tons of information.)  
   
If you wish to contact me, please feel free to leave a message on my e-mail at:  
jacqulynn@-------------
   
Note from Jackie’s mother:  
I have typed this exactly how it was written. It’s important also to note that Jackie has taught herself how to write with her left hand! The entire note taking from all of the research, the original draft, rough and good copies were all written with her left hand through spasms, swelling, cramping and pain over the past 11 months!   
This letter in and of itself has been over two years in Jackie’s thought process. What precipitated this letter into taking form was the devastating news of my mother being diagnosed with cancer and having four to six months to live. Jackie felt an incredible sense of urgency during this time. We were not able to attend “Grandma’s” funeral due to Jackie’s illness.  
In closing, I can only say that Jackie has so much love and compassion in her heart. She cries when she sees a child or an animal hurting. All of her hopes and dreams are but distant memories! She wanted to become a police officer so she could help people! Now her goal is to somehow help one person, just one, to have less pain! This letter is such an incredible accomplishment for Jackie and I am so very proud of her!!  

 A few hours later, she got a reply from...

MEL
September 5, 2005 7:47 pm EDT


to jackie!
I... feel your pain. My RSD is spreading fast, on my next visit I have to discuss with my doctors the chronic migraines and facial/jaw/mouth pain I am now experiencing. I also have my teeth getting weaker, and chipping, but cannot afford a dentist as I am hardly able to pay my dr and shrink.  
You are completely right, more people MUST know about this, especially the doctors who think you are just crazy or a drug seeker. I am dealing with a pain dr right now who does not prescribe narcotics, as I am still in phase I. My fiancee does not know if he can deal with this for the rest of our lives, so our wedding is on hold for now. I would be suicidal myself except for my son, who is 8. I cannot leave him!!! I am 29, and I am in tears thinking that this happened to you at such a young age, as mine has progressed only since 2003. My RSD started in my shoulder and neck, and has moved into my back, other shoulder, both arms/elbows/hands and left leg. It scares me that I am now having symptoms in my face and right leg..... 
I sincerely wish I could help you and wish you the best, if you need someone to talk to please feel free to email me at melbor@xxxxxxxxx  
Your letter is powerful and I hope you have had your mom send it to EVERYONE she can!!! 
I am so tired of being dismissed.... 
I will pray for you, Gentle hugs-Mel 

Thursday, September 2, 2010

Shawnna's Con

Editorial reflection:

I wrote this post on January 24, 2009. That is neither here, nor there, but was, it happens, a significant date. That is my birthday.

This tells me, and I am telling you, in turn, that the circumstances in the post must have been very upsetting. This is not the kind of thing about which one wants to be thinking on one's birthday.

Today, having an additional 20 months of riotous living under my belt, I know that the story I am about to tell is not at all unusual. That's terribly sad, but is, as they say, what it is.

You cannot and should not trust that anyone is who they say they are, is how they claim to be. Unless, of course, you have the means to verify stuff. Unless, of course, you just don't care. Unless, of course, you are one of those people who are brimming-to-overflow with forgiveness.

To update "Shawnna's Con," her latest claims are that she is awaiting a heart transplant, that she had a stroke on Easter Sunday, that her HIV+ daughter is now having her fourth child since diagnosis, and that she, Shawnna, is raising three of those children, that she never made it to Tennessee, but remains in North Carolina. (Note to Self: There seems to be an inordinate number of internet shysters residing in North Carolina. I love N.C. -- I lived there when I was in high school, taught and studied at Duke, and have a long love affair with Atlantic Beach/Morehead City -- so it pains me to say this.)

I decided to use my subscription to an information agency again -- the last time I used it was to discover that my half-siblings, newly admitted into my life, had quite the criminal record. Guess where they live? And before that, it was to discover the deviant goings-on with my cyber-stalker... Who, I kid you not, lives about a half-hour from my sterling half-relatives! What a state!

People with criminal records don't necessarily end up on some sort of exclusionary list of mine. Gauging from the dates of arrest, it looks like my sibs went through a very hellish period, during which they may have been trying to establish some kind of financial independence from The Mother-Unit, although they benefited from having an absolute saint for a father. My Mother is, as the saying goes, a piece of work. Had they ended up hardened felons, incontinent of urine and stool, with needles hanging out of their arms, and their hair all mussed -- I would have understood.

Even my cyberstalker's legal troubles are understandable, stemming as they do from terrible poverty, and, I think, a terrible lack of decent role models and self-esteem. Unfortunately, her daughters now have records, too, for the same reasons. It is a sign of hope, though, that they must suck at thieving, for they've all been caught.

"Shawnna," however, is a con artist and seems to enjoy reeling people in on her fishy lines of drama, trauma. She invades your heart, heartlessly. She has a substantial area dedicated to her crimes on the N.C. Master List of Master Criminals, one arrest coming on the same date of her last claimed thrust-and-parry with Death -- Easter Sunday ("They had to Life Flight me..."). 

Resurrection Jealousy.

I can find no proof online that her recently deceased husband ever existed. Nonetheless, his name has been altered, as well as hers.

The fact that every "disturbed" person I've encountered were met over at the Dr. Phil website is just something I present to you, without commentary. {Though you should see my eyebrows wiggle...}

Hard luck stories are the bread-and-butter of the con, I guess. And I may as well confess, not for the first time here, that I am the World's Easiest Mark. It is great sport among my family and friends to see just how much junk they can get me to believe. I melt at a low temperature, cooing "Oh no, really?" upon hearing their sad, sad sagas.

But I think I am wising up! At least with Fred. He has some "tells" that I can now identify, chief among which is the statement: "This is a true story." But, oh, how it delights him when he can reel me in. I am not going to embarrass myself by laying out the far fetched things I have come to accept as true -- but I recently made mention of one, so I'll reuse it. My former bestest friend in the whole wide world is a gorgeous Iranienne Lesbian (but not, praise Jesus, one of the Militant Lesbian Existentialist Feminists). We met as undergrads, roomed together for a while, and -- even though I screwed up our relationship in recent years -- had a wonderful life together. She just could not believe the extent of my gullibility. One day, we were working on homework in the French Dept. lounge, trying to come up with paper topics for our 17th century lit class. She hit on something she thought I would like -- having to do with that famous classicist Oussama Mon Chénier.

Chenier is a Cajun term, referencing a:
beach ridge, usually composed of sand-sized material resting on clay or mud. Chenier is the Louisiana French term for the oak tree belts that mark the distribution of the ridges in the Mississippi Delta region. In that area there are several sets of cheniers, each separated from, and slightly unconformable to, the next. Some of the ridges have been reworked by waves, and several show a blanket of peat growth (indicating a regression of sea level) covered by marine sediments. The arrangement and composition of these cheniers are taken as evidence of a fluctuation in sea level and have been correlated in time with similar evidence in other areas of the world. (from Britannica.com)

The Shah-Meister regaled me with fond memories of her relationship with this 17th century naturalist, and how she spent many a rainy afternoon stretched out on her bed, thumbing through his great and marvelously illustrated work:  L'Histoire Naturelle des Animaux Sauvages (The Natural History of Wild Animals).  She had never understood why it was such a beloved reference work in Persia but unknown to Unenlightened Westerners.

By the time she convinced me to go and interrogate Professor Aronson là-dessus, I was frothing at the mouth at the thought of the academic wealth awaiting my investigation.  I will just let you imagine my horror at the kindly sad smile which my respected professor assumed about 10 seconds into my presentation of my awesome paper topic...

And then there was the Incident on the Berkeley Pier.

But "Shawnna"?  She's on a whole other level of malevolence.  Given her recent re-emergence (we surmise that she may just have gotten released from prison), I decided to go ahead and post this.  Should you come upon it, Lashy?  I am a Born Again Skeptic, as well as Very Certain Friend to the Woman You Are Trying to Snooker.  So back the fuck up, woman.  I mean it.
***********************************************************************







It's beyond disconcerting: beyond it, though, to I don't exactly know what.

The popular initial reaction seems to be "disappointment." That surely was the killer reaction that worked best on me as a child -- nothing hurt so much as when a beloved adult would calmly (with maybe a Touch of Glum) express disappointment in me and in whatever behavior I had perpetrated.

For 18 months, this woman Shawnna interacted almost daily with me and several other people in an online group that dealt with the vagaries of living with chronic pain.

Oh, put your eyes back in your head! Stifle!

This group put up with *me*, remember. How much time do we spend talking about pain? Almost none. How much time do we spend bitching about doctors and tests and drugs and such, ka-ching? Okay, well, maybe 27% of our text might be so appropriated. Another 52% is dedicated to regaling one another with stories that sometimes tested the boundaries of decency. Roughly 20% of the time, we deal with people who will most likely not be sticking around to become a regular. They are panicked by passing discomforts, angry at the world, desperate for sympathy and compassion, and, occasionally, really in big trouble -- that's when we function like a well-oiled machine and produce names, numbers, web links, contacts, straight up info.

The remaining percentile? In-de-fin-able! That cachet of a certain je-ne-sais-quoi...

There is a woman in this group who keeps me sane. Her latest daily adventures include stealth feeding of two groups of horses that belong to her neighbors -- or, to be precise in one of the instances, the girlfriend of a neighbor who is billeting her horses there for the duration of the love affair. This friend is an animal lover, but not in the extreme -- these horses were not being fed daily and did not have access to [unfrozen] fresh water -- and I think she has reacted as most of us would. Well, not quite. I would be on the phone reporting these neighbors -- in a heartbeat. I do not, apparently, understand the dynamics of life in rural Wyoming, as such an act might well, she tells me, push her neighbors over sanity's edge... and then what would she do?

So, she does the only logical thing.

Excuse me while I laugh a little.

She and her 80-something mother take hay to the two separate pens. I don't know the story of the other neighbor. They wait for the cover of darkness and deliver hay and water. The horses apparently go ape shit every time they see either of the two women, or even their truck.

She has a good heart.

So I am going to go way past "disappointment" and charge on down the path all the way to ANGER. Not at her, no!

At the woman who has fooled her, and me, and lord knows how many others. We nicknamed her Shawnna. She was thrilled when she was given a nickname. It made her "one of us," one of the gang, party to the inner circle, whatever -- it marked the moment when she had definitively snookered us all.

I spent part of the day digging up every post she had ever published at the web site that hosted our laughter-loving chronic pain support group. Somehow, she never expected anyone to piece all the disparate parts together. Well, I got right to it, didn't I? It just took me a year and a half.

This is the story she has written, in bits and pieces, some meant for one group, some for another:

She is 43. She just recently lost the triplets she was carrying -- made it to 6+ months, though. There are several posts about her inability to go into the nursery and pack up the tiny clothes and take down the cribs, maybe throw a little paint on the walls, scrape those silly stencils off, try to sell that stupid rocking chair on eBay.

That was mostly for an online grief support group that rallied around her as she faced the anniversary of the triplets' death, and with whom she went on to share her childhood experiences of incest. Eventually, I guess, there was a strong sense of incongruity, and she moved on to the more appropriate Childhood Sexual Abuse Survivors Group, never speaking of the dead babies again.

About that same time, she approached us with a need for advice about having, or not having, a hysterectomy. The reason given was "pelvic pain." For reasons that I could never figure out, her surgery was supposed to take between 6-8 hours and might result in her death, or a colostomy. (Tonight, I relish that symmetry: her death or a colostomy. I like those odds.) She said she'd had 15 previous abdominal surgeries.

Let's see... She suffered from cardiomyopathy and a well-controlled seizure disorder, although she had a seizure on the operating table during her last operation and... you got it! Almost died.

"I almost died" could have been the chapter heading for most of her revelations.

She had three adult children. Her son was in prison for murder. Oh. As it happens, her brother was going on trial as a serial killer, and she lived in dread of having to testify. Her oldest daughter was a heroin addict with two small children. She popped into the narrative as a regular character when Shawnna decided she should have AIDS, abandon her kids (the long suffering Shawnna and her husband Rudy dedicated themselves to raising them, of course), and run off to New York with a no good man.

Shawnna's youngest daughter was a straight-A student, finishing her first year at college, and had never caused, or been in, any sort of trouble, ever. With the now added burden of two toddlers to raise, we suggested to Shawnna that her "good" daughter might be able to help out on the weekends. "Oh no," we were told, she did not want to be a burden to this young one who was doing so well.

Not even after her surgery went awry and she was mostly bedridden and living on methadone and percocet (Hey! I resemble that remark!) would she consider asking her daughter for help. She would carry on, somehow -- taking care of those two grandchildren, volunteering at their schools, working at the funeral parlor (part-time) and taking care of what she called her "wifely duties" with Rudy. [Prior to working at the funeral parlor, Shawnna said she owned a Home Health Agency, which she loved, as it allowed her to use her training as a *nurse*! I guess that is not an altogether uncommon move, to go from the healing arts to the death business?]

Of course Shawnna's surgery did not go well! This was surprising, as it took place at UNC-Chapel Hill (those slouches!). Would you believe that the numb nuts left a sponge inside of her? She ended up needing more surgeries because of their horrid oversight.

Then began the Saga of the Vaginal Bleeding. I know that it stretches the bounds of your credulity, but it was only at this point that she lost me as one of her dedicated cheerleaders. Because she kept bleeding and bleeding, going in and out of the hospital several times a week. I have also had a total hysterectomy and my crude understanding of anatomy informed me that there just are not that many sources for such bleeding... Somehow, I assuaged my suspicions with the reassurance that I apparently did not know everything, and that Shawnna was surely cursed and being used by God to do a rewrite of the Book of Job.

(Book, shmuck! I forgot to mention that she is an author of two books. No, I haven't been able to find either one.)

Oh, I grow weary.

Well, what is left to Shawnna's Tale? Ah, yes. Rudy almost passed away about a year ago -- he had a major stroke at the age of 33. He up and died a month or so ago -- he was out mowing the lawn and had a massive heart attack.

My tenderhearted Wyoming friend prepared herself for service -- a plane ticket, her own home and hearth in order -- and waited for details. Waited and waited. Shawnna was impossible to reach.

Suddenly, she posted a message saying that she was going to relocate to Memphis, Tennessee. I had begun searching for a death notice, checking obituaries in her area, then anywhere, then under any mistaken spelling of the poor dead man's last name. Nothing, nada, zilch. I asked her about it, finally, and was told that her world was turned upside down (understandable) and that Rudy's adult son from a previous marriage was handling those details.

Okie-dokie, then!

After a bit, she reappeared, reintroducing herself this way in an email, afraid, it seems, that the various plots of her story might have become stale:


I know that it's been a very long time, I'm fine. I have 4 grandchildren now, and all by the same daughter. I have three of them. I had a stroke on this past Easter Sunday but I must say that with some physical, and speech therapy I'm doing much better, I have been missing both you and M but I almost lost my  mind girl after my husband passed away. I'm much better know, and I've learned to cope with it. I love you just the same as I did one year ago girl!

Love,
Lashy

Finally, a period of relative calm, with only occasional hospitalizations for congestive heart failure interrupting. She was off to her new life in Elvis Land.

Except that we heard nothing and could not reach her. Finally, we received a message that she had suffered a major heart attack while driving...

With a familiarity that suddenly *was* breeding a major pile of contempt, we could not contact her at the hospital she was supposedly at and so on and so on and so forth.  In the past, her "good daughter" would appear online at these times of crisis, and promise to relay messages, etc.  There appeared to even actually be such a daughter that my friends were able to reach by phone.  Something in that precious mother-daughter relationship became irrevocably strained at this point, however, because Lashy wrote, out of the peculiar blue:

She  is  doing well, she is studying at The University of Winston-Salem now. She is in her 5th year of schooling. She is still studyimg to become a Psychologist. But guess what? She doesn't even call me, come to see me. She didn't even come to the hospital after I had the stroke, and I had been life-flighted there to Winston-Salem!!!!! I was sooooo hurt. I just couldn't believe that she didn't come to see me. I haven't heard from her now in almost a year. I just this information from her father. But  I am not going to sit and worry about what is going on, I love her, have done not one thing for her to treat me the way she's been, and one day she'll regret the time that we didn't share together.

There is, of course, no University of Winston-Salem, so I assumed it a reference to Winston-Salem State University.  But it, of course, has no graduate program in psychology, but does have a good-looking undergraduate BA degree in the field.

It was a great set up.  Now Good-Daughter-Turned-Mean-Child could not be relied upon as a benevolent player in Shawnna Land.  You can't trust her or believe a word she says!

That fix was apparently not enough, however, because Shawnna went on to have Good-Daughter-Turned-Mean-Child suffer a stroke, herself, and be put, herself, on the "transplant list." Again, Lashy was kind enough to provide all sorts of contradictory written information, though she never seems to completely hoist her own petard.  This is a letter she sent to my good friend during Scene 4 of Act 3, or whatever we are to call this internet con drama.  It's one of her more elaborate, and the construction is interesting, particularly the opening gambit.  Hi, it's been forever, my dying-with-AIDS daughter is such a whore... my Good-Gone-Bad-Now-Redeemed-Again daughter is in ICU... all summed up by the telling, "Oh my God girl!!!! What more can I deal with huh?"

I don't know the requirements for receiving hospice care, but apparently they are not as stringent as I believed!


----- Original Message -----

Hey Girlie,
I know that it's been a while that we've spoken. How has everything been going for you? I have some very disturbing news. I just found out very recently that my last granddaughter is not my daughter's husband's daughter!!! No, her father is some other low-life piece of shit that roams the city of Fayetteville! The DNA test just came back last week. I am so through with my daughter do you hear me! So now we've got to try and find this someone to let him know that he is now a Father. I spoke with my daughter and asked her what the hell is she thinking? Not only were you unfaithful in your marriage but you had unprotected sex with someone that you really don't even know!!!! She tells me that she's been knowing this man for a year! Uh....wow...a whole year!. Please, give me a break!

Plus the fact that T (my youngest daughter) is in ICU and has been for the last past four days, we found out that she has inherited my cardiac condition. She has an enlarged heart and went out to the emergency after feeling very ill. She was having difficulties breathing and was having some swelling in her legs and hands. Oh my God girl!!!! What more can I deal with huh? But the good news is that she's doing better and the Physician told me that he'd be able to step her down off of the milirinone lactate and put her on an oral medication at this point. So hopefully she's be discharged at some point this coming week. 

I always feared one of my three children inheriting my cardiac condition and the one that has her shit together is the one that has been crippled with this enormous problem. I'm very afraid that this will limit her ability to have children one day when she's ready. All I can do is guide her and show her how to deal with this cardiac problem. They have put in a picc line so that she can be administered the milirinone, the same medication that I use on a continuous basis here at home. My picc line has been sewn in place though.

**[Lashy simultaneously posted elsewhere that Good Daughter Gone Bad was comatose, had had a stroke and suffered severe neurological deficits.  Milirinone (sic) lactate?!  Yowza!  In the little bit of reading I did about the drug, one thing was pretty doggone clear:  "treatment with this drug usually does not exceed 5 days..."  This archived drug label made it clear that this warning against longterm use was not lightly made:

Whether given orally or by continuous or intermittent intravenous infusion, milrinone has not been shown to be safe or effective in the longer (greater than 48 hours) treatment of patients with heart failure. In a multicenter trial of 1088 patients with Class III and IV heart failure, long-term oral treatment with milrinone was associated with no improvement in symptoms and an increased risk of hospitalization and death. In this study, patients with Class IV symptoms appeared to be at particular risk of life-threatening cardiovascular reactions. There is no evidence that milrinone given by long-term continuous or intermittent infusion does not carry a similar risk.]**


I was in the hospital for my birthday, (7th January). I was in CHF and renal failure. I am better now and hopefully I won't have another hospitalization for some time.

I allowed my daughter to come over to spend a few hours with all of the children during the holiday and she didn't even think or consider buying either child anything for the holiday! I was very disappointed in that too. I have just come to realize that my daughter will always be selfish, bottom line.
Have you talked with M lately? I would like to go and see her for my 1-week vacation this coming April once the kids are out for Spring-break but I haven't heard back from her to confirm. I would like to come see you one Spring/Summer as well.

I really miss you guys so much. I feel so bad sometimes girl that it takes all I have just to get up and move around each day. My cardiac health is slowly declining, and I can really feel the change. I have hospice coming in each day and they've helped me aloft as far pain relief, and making dr's appt's for me.  And I have a CNA to come out each day for three hours. She helps with laundry and running errands for me.
I just wish that I could feel 30% better.

I had a difficult time yet again this year during the holidays because as you remember Rudy passed on the 6th December. I must admit that having friends and family here for the holidays did distract from the depression that I was feeling but, It was still difficult and I guess that it will never really go away.
Well Sweetheart, I've taken up enough of your time with my whining so I just want to let you know that truly I love you very much and because I may not post or send messages as often as I did before, doesn't mean that you're not on my mind. I look forward in hearing from you soon....Talk later
Love,
Lashy
P.S Have you heard from Prof? If so, please give her my hello's.......................
[Prof, here, chuckling...]

Somewhere in all the chaos, Lashawnna began to mention LVADs, and it was never clear whether she had one, but it became something of an obsession, but -- as you might expect -- the LVAD stories came with their own healthy quantity of red flags.  Small flags, maybe more of a bled pink than a screaming ninny of a cerise.  Things like continued smoking, something that I'd think one might give up if faced with left ventricular failure.

I was contacted by a very nice guy who is an authority on LVADs and whose blog is dedicated to helping others learn about the life-saving devices.  Shawnna was driving him a bit mad, contacting him repeatedly with requests that he call her, and performing her typical zero-to-sixty insistence on intimacy.  You know what I mean!  She glosses over the normal periods of making acquaintances so as to rapidly insert herself and her confusions into the mark's life.  Unfortunately, she just came off sounding weird to him and he did an internet search... finding, eventually, "Shawnna's Con."

An aside:  What a wonderful guy, what a wonderful attitude!  He is steeped in gratitude, and it shows -- well beyond words, it shows in pictures and videos, it shows in how he reaches out to give others a hand up.

My capacity for playing the fool has amazed me. I still want the thousand dollars back that I gave to someone I "met" online in an osteonecrosis support group.  I did not hesitate to help her pay her electric bill so that the utility could be turned back on, keeping her young children warm. One of her sons was very ill, she said, and she couldn't afford to take him to the doctor.  Are you sitting down?  Turns out she had other uses in mind for my money, uses that were more in the line of "entertainment."  Well, we are all deserving of fun... Right?

I never gave Shawnna anything material.

No, I cried with her, listened, tried to help and advise, pitied and prayed for her -- and for "hers," who were always so deep into trouble, lost without her able help and guidance.

I cannot even laugh at myself as I begin to seriously fret over who is taking care of those beautiful, innocent grandkids.

Because I cannot know what tidbits are true, which are false, which are more properly interpretations.  She may have a failed heart, her daughters might be equally ill -- one sticken with Lashy's own disease, an inheritance, the other with AIDS, Lashy's emblem for "bad."

The proliferation of grandchildren, all born to an HIV+ woman, is at the heart of this con's tale.  Babies, some of them dead (her opening at Dr. Phil's, remember, was that she had just lost triplets), all of them displaced, are what's the matter.

I wish I understood.

It turns out, I believe, at least, that Shawnna has an accomplice. So I -- and others, especially one kind spirit in Wyoming -- are waiting for the other shoe to drop in the saga of Shawnna's con.  She wants to set a trap, and has, probably.  I just want to issue a Public Safety Announcement -- which is what I suppose this post was supposed to be.

But oh, Dear Readers, there was one wondrous development, just a few months ago, and I will end this rambling "cautionary tale" by copying below a rare moment of love and warmth between myself and this con artist.


You can imagine how thrilled I was to be able to notify Shawnna, in January 2012, that there had been a resurrection, good news of the miraculous sort:

lashawnna wrote: 
"Morgan and Dianah I know that it's been a while since I last spoke to either of you, I have been really having a hard time dealing with the death of my husband, so much so that I had to relocate to another home, too many memories.[...] Prof, I have really had you in my thoughts and prayers and I hope that all is well with you. I have had to really dig deep for my sanity, for a time there, the walls started to close in on me and I felt as if I was losing sight on reality. I couldn't sleep because I was in constant thought of Rudy. I have lost 39 pounds. When I first started posting, I wore a size 14 pants, now I am wearing a size 5/6."

i, profderien, wrote: 
hi lashy,
long time, girl, long time!
but i am so glad to be able to come to you with good news.  
heck, it's great news!  
are you sitting down?  no?  well, take a second and sit yourself down, because i don't want you to faint and hit your head, thereby sustaining a life-threatening subarachnoid hemorrhage or possibly fracturing the medial epicondyle of your humerus (the "funny bone"!).  heck, the joyful shock of what i am about to disclose to you, our dear loving lashy, might cause your cardiac muscle to shift into overdrive.
it's PHENOMENAL news!  it's put-it-on-the-doctor-phil-show-it's-so-good news!  (seriously, my friend, you would make a fascinating guest.)
ready?  are you sure?  okay, here goes:
RUDY IS ALIVE AND WELL AND WORKING AT WALMART!  It's a freaking miracle of humongous proportions.  
no, i am not pulling your tiny size 5/6 leg!  it's time to have a really big, fattening meal in celebration -- but cardiac-friendly, of course, maybe an arugula salad dressed with balsamic vinaigrette, some poached salmon over a lovely parsnip purée. (i'm hungry.)
you probably don't believe me, i know what a stickler you are for truth, justice, and the american way -- and here i am, saying rudy (by whose grave you wept and loss scads of weight) -- that scumbag who pretended to stroke out while mowing the lawn -- here i am saying that your husband rudy is flaunting his status as a living organism... all over facebook!
i wasn't sure, and again, out of respect for your reliance on honesty, i asked someone who knows what rudy looks like to take a gander at his profile picture.  i was assured that "yep, that's him!  the no-goog pretending-to-be-dead bozo!" 
i know, this news is really a mixed bag.  part pure relief (He Lives!) and part ultimate frustration (How Could He Let Me Grieve and Waste Away to a Size 5/6?).
but you are nothing if not a strong woman, accustomed to adversity (good lord, when i think of the tragedies your family has suffered... the loss of your triplets, your brother's murder conviction, your son's murder conviction, your daughter's HIV, your other daughter's cardiomyopathy, your own cardiomyopathy, your multiple and simultaneous needs for a heart transplant... why, it boggles the mind, if not one's credulity!).
i gotta say, though, lashy... i believe i would divorce the bastard.  no doubt you have moved on in these intervening years, and some other lucky man has scooped you up.
well, that's about all.  i hope you can get over the shock of it.  this is a great place to vent, though, you know?  everyone here is like FAMILY, gullible as all get out, willing to lend you sympathy, understanding, love, and probably a ten spot or two.  you can say *anything* here.  it's a safe place, where no one trolls for victims to exploit, where no one even considers playing a con.
all the best,
prof