Showing posts with label Hannah. Show all posts
Showing posts with label Hannah. Show all posts

Monday, December 16, 2013

My Hero Hannah Needs Your Help

Please excuse this unusually terse entry -- more on that in the next terse post -- but time is of the essence!
[If you don't recall Hannah, click on her bolded, underlined, and capitalized name just below this, my favorite photo of her, called "Hannah's Crane."]



HANNAH is my hero because:


  • she faced osteosarcoma like a mentally seasoned champion, not a young, untested girly-girl
  • with her family, she chose a relatively new option for the surgical removal of the tumor in her leg -- rotationplasty
  • she faced recovery and rehab from the rotationplasty with courage and a grand work ethic
  • part of the therapy for osteosarcoma, as for most cancers, involved radiation and chemotherapy, and these things, too, she struggled through with beautiful style (as beautiful as one can be whilst throwing up)
  • just when all seemed well, hannah developed one of the side effects of her chemotherapy -- leukemia (and if that isn't a kick in the stomach, what is?)
  • as if that were not enough, the osteosarcoma reared its ugly head again, traveling to her lung, and she underwent surgery to remove that cancerous nodule.
  • she undertook this challenge as she did all the others, in beauty and ferocity
  • but still, she needed a bone marrow transplant to defeat the leukemia, a truly arduous and scary procedure
  • now post-transplant, she and her family live with the fear of rejection syndrome and further spread of the osteosarcoma, so every symptom that you or i might consider trivial, they must treat as potentially life-threatening and make a run to the doctor or ER...
  • and they do all these things with grace, humor, and the requisite NEGU attitude (Never Ever Give Up)


I think you get the gist of it, yes?  She is doing well but the struggle is not over, and while she became my hero when I read about her choice of the rotationplasty at the beginning of her journey, I imagine that as she grows, in emotional and physical age, that choice will provide her with some challenges as well as its many benefits.  But that's ME talking and projecting my weaknesses onto Hannah.  Excuse me!

Her mom posted this request today and I hope as many of my bazillion readers as can will place an order to help them out with the medical bills and the bills of daily living that have had to be pushed aside for two years.  Shoot, I will project one of my major pet peeves onto the Smith family: parking fees! Never mind the cost of all the traveling they've had to do for treatment, just think of the darned parking fees at all those hospitals, doctors' offices, and "medical buildings."  I may hold a fundraiser for myself one day, just for parking fees...

Oops.  Train of thought, off the tracks once again.

Here is Hannah's Mom's message:


12-16-13
1 hour ago
Hannah has designed a T-shirt that is on her favorite color. It is a fundraiser and we need your help. You only have until Thursday to pre-order. $15 each and will be shipped 2 weeks after the end of the last order date. Our goal is 150 shirts but we only have 89 ordered so far. Can you help? Here's the link:

https://www.booster.com/hannahsmith?share=6511387163898591


Thank you for your help! 

© 2013 L. Ryan

Tuesday, September 10, 2013

Hannah Stars on the Today Show




I haven't written in a while about Little Miss Hannah, My Hero.  She is someone I think of on mornings like this one, when the whole night was spent in spasm, and Buddy ate one of the cables to the DVR.  Of course, normally, I'd comfort myself with music from my well-loaded, super-soothing mp3 player... but Buddy ate the last of my earbuds a few days ago.  It's not fair to Fred to then blast music on the CD player on my bedside table... although, right now, I could probably get away with it, because... Well, remember that ear infection Fred had a few months back?  It has returned, such that he has completely lost hearing in his left ear and perceives things in a distorted fashion out of his right side.  So I figure that blaring Pink Floyd won't endear me -- any more than I am already endeared -- to the belovèd Fredster.

No, I am NOT weeping... that's just the state of my right eyeball!

Yeah, so when things are this fun around here -- and did I mention that Fred the Chef made himself a burger bonanza at about 2 am?  And that he doesn't understand the concept of GREASE, or of those lovely little things I purchased that fit nicely over any frying element to prevent GREASE from covering, say, your girl's cute little bright red enamel kettle?  The damn thing practically slipped out of my hands when I picked it up to get coffee started.  Umm, where was I?

Oh, right!

Hannah has had *real* troubles.  Not the kind that go away with a little elbow grease and some electrical tape.  Not the kind that can be overcome by the application of bad wit and an even worse attitude.

I know this is weird, but I have admired and loved Hannah since someone first referred me to her CaringBridge site sometime last year.  At that time, she had been diagnosed with a pretty straightforward osteosarcoma in her leg.  That sounds simple enough, doesn't it -- "she had been diagnosed with a pretty straightforward osteosarcoma in her leg."

Well, for an athletic, sensitive, active, highly intelligent young lady, that had to be devastating.  But she soldiered on... and I admit that kind of worried me, as I do know something about the dangers -- the future emotional dangers -- for kids who just soldier on through hard times.  I had a somewhat dysfunctional father who harangued into my thick head that I was to take any troubling issue and put it in a box (said box residing inside the aforementioned thick head), and "never, ever open it again."

THAT'S the healthy way of addressing problems!  Might that be behind my tendency to sleep for a week when confronted with some badass issue?  I know -- get over it!  Well, like everyone, it does sometimes feel like I've spent my entire freaking life getting over the emotional dysfunction gifted to me by the Parental-Units... and I'm also highly cognizant of the fact that I am wayyyy past "grown," and responsible for myself and my actions/reactions.

So I still spend time looking for people from whom to learn, for people who seem to have it together, for people whose natural inclinations, good upraising, and excellent natures guide them in the right way.  The Tao, I'd have said at one time.

Such is Hannah.  She and her family studied the various surgical options for her osteosarcoma -- the one sure thing is that these tumors must come out, and removing tumor from bone almost always involves hugely traumatic, life-changing surgeries, mostly amputations.  In recent years, though, another very creative option has gained in popularity, especially for children.  It allows them to be fitted, once healing has been accomplished, with state-of-the-art prostheses that permit continued participation in sports, and, really, given the optimism and brilliance of kids -- participation in anything.  It is a procedure called a rotationplasty.  If you go back and read some of the initial posts on this blog about My Hero Hannah, you'll find better explanations and a video that her mom recommended.

I will be honest.  It turned my stomach when I first read about it.  I cried.  Then I watched that video and others, and thought about the many heroes I met during my brief stint at the Shepherd Center, and the bravery of people who are not willing to cave in to circumstances, who are claiming a normal life, and know to do so at very tender ages.  And I straightened up.  To rehabilitate my Dad's bad advice mentioned above, he also hammered into my head that I should "straighten up and fly right."

What can I say?  The man was a career officer in the United States Air Force.

Ah, but Hannah's road did not get easier, even after the rotationplasty and the process of rehab and fitting prostheses.  In one of the saddest twists that I've ever heard of, one of the side effects of the chemotherapy she underwent for the osteosarcoma is... leukemia.

In a double, triple (it's hard to keep count) whammy, she developed leukemia, and they also discovered nodules in her lung that were metastatic cancers from the original tumor in her leg.  So brave Hannah now had to defeat cancer again, and ultimately required a bone marrow transplant, which she just recently completed.  To be honest, the reason I've not written about her for a while is that, although the initial signs are that the transplant has gone wonderfully and has grafted completely with her immune system... I've been feeling like a jinx.

But I'm over that.  It's time to celebrate Hannah;  it's time for Hannah to do all her grieving and processing, healing and living.  It's time to take that deep, cleansing breath.

So her mom has been very excited about Hannah having been chosen to be featured in this Today Show segment.  It got bumped a few times, but finally aired today.  She looks beautiful and radiant to me, after having seen nothing but pictures of her during the worst of times.  She faces many a challenge, the first being to process all that happened to her with such rapidity, the next being the many daily obstacles requiring adjustments (pieces of cake, I'll wager, though irritating as all get out), and then that future road, of which none of us can ever be sure.

But there is no one better prepared, no one with better support, and no one more heroic.*

*Nota bene:  I DESPISE the concept of the "exceptional" sufferer, be it a patient with a physical illness or challenge, be it someone mired in the worst of the universe's circumstances.  There is no requirement, that I am aware of, that people must do exceptional things, all the while smiling and encouraging others.  I am more comfortable around someone who throws the occasional fit and curses God, figuring, I suppose, that these are the people who really are in relationship with God.  So if Hannah were ever to pout, act like a brat, regret what she feels she's missed... that sounds perfectly normal and fine.  It's just that she is not going to ever be STUCK there...  It's not in her nature.  If I've envy, well, that's where it lies.

So here she is, star of the morning news shows!



Visit NBCNews.com for breaking news, world news, and news about the economy




© 2013 L. Ryan

Monday, June 17, 2013

Hannah Prepares to Kick Cancer's Booty

A note from Hannah's mom was posted on Caringbridge today:

And so we begin the 3rd chapter in kicking Leukemia's tail. Hannah was admitted last night and already had her anti-seizure meds to counteract the chemo. This morning started HEAVY chemo. Her immune system will be killed off over the next 10 days. BMT [bone marrow transplant] infusion will be on the 26th. We are all ready to get this behind us! 
Go, Hannah, Go!

Tuesday, May 7, 2013

Update on Hannah



It's been a while since I've updated my Dear Readers on Ms. Hannah and her progress.

To briefly skim her story:

Hannah was diagnosed with osteosarcoma that involved an area just below her knee.  The standard treatment is chemotherapy, radiation, and amputation.  Hannah made the courageous decision to go with another option that is slowly gaining in popularity, despite its seemingly radical nature.
She opted to have a rotationplasty, in which the cancerous area is, indeed, amputated, but the foot is reattached, backward, essentially to the knee.  It's much more complicated than that but what it allows is for the later fitting of some awesome prosthetics that permit people to remain very athletic and active.

She had the chemo and radiation.  She had the radical surgery.  She worked like a true champ in Physical Therapy and was doing very well.

Do you know what one of the side effects of the chemotherapy is?  One of the leukemias.  And yes, Hannah has developed leukemia.  She also was found to have a nodule in her lung that was a spread of the original osteosarcoma.

So she has had to change horses midstream, as they say.  She is now undergoing the preparatory chemotherapy to set the stage for a bone marrow transplant -- a European man is a perfect match, "except" for a few compatibility issues in typing.  I know, I know... so he's not a perfect match.  Near perfect!

At the moment, while her counts are down so low, she's been hit with some viruses, precisely at the time when she has NO immune system with which to fight back.  Her Mom is feeling low, too, because she thinks that she is now catching a cold, which means she cannot be a bedside cheerleader until she's well.

So... give a thought to Hannah tonight, and her family, particularly her Mom.

She is one plucky kid, and she is my hero.  When I get all slobbery pitiful about missing a shoulder and not being able to move a leg... I think of this girl in her heroic "crane" pose, in her quest to get back on the soccer field, and in the pool, and I read about her doing the very hard PT work without a word of complaint... and am so humbled.

From Caringbridge:

FEBRUARY 7:  Please forgive my tardiness in updating you all on how our Hannah is doing. It has definitely been a crazy week since she got her new diagnosis last Wednesday.

Hannah is still recovering from lung surgery. As of today they still are NOT going to remove her chest tube. There is a bubble in there and it has to be gone before they can take it out. First prayer is that the bubble goes away and she can get that tube out. It is terribly uncomfortable and painful for her when she moves around.

As soon as she is cleared from her surgeon, she will go straight to the 9th floor to begin chemotherapy treatments for her AML (Acute Myeloid Leukemia). She will be in the hospital anywhere from 4-6 weeks straight depending on how fast her numbers go back up after treatment. She cannot leave the hospital until her numbers are cleared...then after a couple of days at home, she will go back in for another round of chemo with the same parameters. After that she will have to have a bone marrow transplant. This is as far as we know for her treatment. Once she's past the transplant, we will see where we are going from there to get her in remission.

As for the tumor they took out on Monday, it was confirmed as Osteosarcoma. While we are all disappointed that it recurred so quickly (only 2 months), the good news is they did get all of the tumor and because the margin around the tumor was healthy cells, we know they got all of it. That means, at this point, there are no plans to put her through treatments for Osteosarcoma. We are so grateful for this "silver lining" in our very dark cloud.

We are so grateful for all of the prayers and positive thoughts coming our way. Hannah is in wonderful spirits, as always, and is ready to fight this monster called cancer. I will update you when I know more.

APRIL 19:  Just had another big informational meeting about Hannah's bone marrow transplant at St. Louis Children's Hospital. We know that Hannah's donor is a man from Europe and that he is a perfect match based on the criteria however there are a few things that could be a potential problem. It's a lot of medical terms so rather than go into a long explanation I'll just say she will have a heightened risk for GVHD (graft vs host disease) as well as CMV. His blood type is A+ and Hannah's is O+ so initially there could be issue despite them taking out the red blood cells. There are also lots of meds she's going to take for prep for the actual transplant. Also they pushed back her transplant date to June 12. Sooo many hurdles yet to jump. Please pray everything goes as planned with no rejection or problems. I feel so overwhelmed with all of this...soooooo overwhelmed! :'(

TONIGHT:  Hannah's still feeling rotten. Her ANC is back down to 0, but that's to be expected. These viruses (rotovirus is one of them) are kicking her tail. Still coughing and runny nose. Had to have 2 units of blood today b/c her hemoglobin was WAYYY low. Had platelets yesterday. She's really getting frustrated and down about it all... she told me today "I just want to be done!" Translation: Ive had enough of hospitals and medicine and doctors and all of this. She and I had a bit of a cry together, which I think helped her. Another hurdle for me (I know I never post about myself so please forgive me) is I feel myself getting sick too. If I'm sick, I can't be on the floor, meaning I can't be with Hannah. This is all so overwhelming! I can't be sick! My Hannah needs me! :'( 





Uploaded to YouTube by mayoclinic on Sep 3, 2010:  "This is a pre-surgical video which describes rotationplasty, who the procedure is appropriate for and possible complications. This video depicts the process of being fitted for a prosthesis and learning to use it. The patient describes her active and satisfying life after rotationplasty, her emotions and the process of adjusting to living with a prosthesis."

Monday, February 18, 2013

Something to consider, Dear Readers

No offense to my "cancer kids," but if you all would puh-leeze stop dying and relapsing, I'd appreciate it.  Just kidding, young ones, there's a whole host of you who've graduated from "The List of Four" and are now in college, back in fourth grade, on the swim team, and just generally kicking cancer's booty.

Miss Hannah, looking like she might wanna chew glass... but lovely and colorful, as usual! 


I want to talk to my Dear Readers about Miss Hannah -- yes, my hero.  If you've been following my logical and well laid out presentation of her story, you know that she recently suffered a relapse of osteosarcoma, with spread to her lung.  The good news is that a (relatively) simple surgery may have caught it early in the form of a nodule with clean edges.  So, that's worth a "yay!" -- just don't scare your co-workers with too loud a scream of joy.

The down side of chemo for osteosarcoma is the "side effect" of leukemia, which Hannah now has, as well.  That's worth a scream of another sort, and you probably should wait until you've some privacy before letting loose.

But you know me!  I'm not one to wallow in self-pity, oh no!  And in this case, since I am not the one battling two cancers at once, why should I?  Sorry, I got confused there for a moment, or a decade...

So here is the deal. Be a bone marrow donor, because that's what Hannah is now working toward.  It's an arduous process, and she is, of course, taking things zen-like, as they come.  But her transplant coordinators and family can't afford the luxury of laying around doing chemotherapy, relaxing in that comfy hospital bed, and chowing down on jello.

This is the latest post from Hannah's mom, shared at her CaringBridge site:


Today starts week 2 of this 4-6 week stay. She has 3 more days of chemo (including today) and then we wait for her counts to come back up before they let us go home for a few days. 
Today I spoke with the head nurse for Dr B...my other kids were tested to see if they are a match for donating bone marrow to Hannah. We got results...NONE of my other kids are a match for Hannah. The nurse said "they didn't even come CLOSE to being a match". *sigh* Soooo...plan B. They've already started the registry search. Because so many of you have offered to be a bone marrow donor for Hannah, we are in the process of putting together a donor drive. I will let you know when I have details. 
Thank you for keeping us uplifted in thoughts and prayers. 

From the National Marrow Donor Program, here are some frequently asked questions, with answers!  


Matching a patient

Deciding to donate

Donating bone marrow

Donating PBSC

Learning about the patient


Wednesday, January 30, 2013

UPDATED: Hell's Bells: Pray for Hannah

all previous "Hannah" posts can be found HERE.

UPDATE 2/2/2013:  From Hannah's Mom:


We had a meeting yesterday with Hannah's oncologist. In addition to the Leukemia, they found a nodule in her right lung. They believe the Osteosarcoma is back. It looks like she now has 2 types of cancer she has to fight. Hannah will have another Thoracotomy Monday morning to remove the nodule. It will be biopsied to confirm it is Osteosarcoma. We are devastated to say the least. Once she has healed from surgery, they will begin chemo for the Leukemia (AML). We have a very long and terribly difficult road ahead of us. Hannah is in very good spirits and is doing quite well under the circumstances. Please continue prayers for all of us. 
**********          **********          **********          **********          **********


I love this confident face...

Aw, hell's bells.

This breaks my heart.

Hannah, my hero, the little girl who had the rotationplasty last year following discovery of osteosarcoma in her leg, now has leukemia.  Her mother just posted this plea, which I pass along to you, as I remind myself that even heroes need loving support:

Worst nightmare confirmed. They found Leukemia in Hannah's biopsy. On our way to St. Louis Children's Hospital now. Pleeeease pray! :'( 
In case you've forgotten Hannah's heroism, it comes not so much from being stricken with cancer, that happens... It comes from choosing to treat her particular form with a fairly new and radical surgical option, the rotationplasty.  Here's a great video from the Mayo Clinic about the surgery:



Uploaded on Sep 3, 2010
This is a pre-surgical video which describes rotationplasty, who the procedure is appropriate for and possible complications. This video depicts the process of being fitted for a prosthesis and learning to use it. The patient describes her active and satisfying life after rotationplasty, her emotions and the process of adjusting to living with a prosthesis.

Here is my favorite photo of Ms. Hannah, My Hero, as The Crane:

From Prayers for Hannah
There shouldn't be profanity there where Ms. Hannah is... but you'll excuse me this:
DAMN CANCER.


addendum:  some fast reading and reminding allow me to share that the only thing that heralded the development of the leukemia was a sudden bad rash over her upper body, for which they went to the logical healer, the dermatologist.  it was his biopsy that led to this second cancer diagnosis.  apparently, one of the curses of chemotherapy for osteosarcoma is that it puts the patient at risk for... leukemia.  now that is one sucky, sucky side effect.

Thursday, November 8, 2012

Getting it all out, at once...

If you don't hate cancer, you ought to.  I take that back... maybe you are different from me -- it happens -- and you come at cancer with your love of life and a refusal of hate, a refusal to hate anything or anyone.

I'm resigned to not being that great of a person.  I've almost come to accept Nate Silver's probabilities that I'll go to Hell.

There is, right now, too much cancer in my life... and it's not even in my life, properly speaking.

It's in my friend Joyce's life, as she watches her husband Billy struggle to breathe and lose, perhaps thankfully, his grasp on reality.  She's amazing. Trust me on that...

Joyce and Billy on September 15, 2012

Joyce wrote on her Facebook page, this past Monday:
Billy's nurse just left, he has gone downhill very fast. She said there were NO lung sounds at all on the right and very little on the left. He has been out of it, talking to himself and people thats not there. He is sooooo worried about leaving Brian, when we ask him what he said he will say he was talking to Brian, and Brian isn't here. 
Brian is Billy's oldest grandson, who knows him more as a father...

Cancer is still in Kate McRae's life every day, too -- but she's been doing wonderfully, and hopefully will continue to be cancer free.  She and her mom Holly, and her dad Aaron, sister Olivia, brother Will are in the midst of that unimaginable angst of it being "MRI" time.  Oh, and she has pneumonia.  Holly wrote, a few days ago:

This will be 6 months out of treatment, and my heart continually reminds me that she relapsed at 9 months out of treatment last time. We pray for CLEAN scans. Not just to the Dr's eye, but that there would be distinctly no cancer cells left in her body. None. And no confusion upon reading the scan.
Kate McRae, courtesy of her CaringBridge site


HAPPY UPDATE for Ms. Kate:   "No Evidence of Disease!!!!!! Some of my favorite words!" Yayyyy!  That was Holly's tweet after Kate managed a 3-hour MRI without anesthesia, because of her pneumonia. The funniest tweet came next:

Kate: "Mom, I love you, by please don't shout it out about my MRI. They are strangers. You are embarrassing yourself. "
Not even close, Ms. Thang!

Moving on... of the other children I follow (I try to keep it at four... no idea why, but four it is) -- my personal hero, another Ms. Thang (check out her bangled-braceleted arm!), Hannah, has finished her chemo and despite a struggle with its side effects, is home.  Her nonchalance in the face of rotationplasty made me feel quite ashamed at my regret at losing a shoulder, and her courage before all that followed made me a teeny bit less self-absorbed, hard as that may be for my Dear Readers to believe.

Hannah's photo courtesy of her CaringBridge site
My third kid is also hanging in there, though his path is rough:  Sweet Braden and his super-courageous mom Maranda.  His most recent MRI?  Maranda wrote:

Brayden's MRI is completely stable. The Dr is very pleased. We are so relieved. Happy tears all around. Thank you is not enough, but it is all I have at the moment, plus lots of love from us.

Brayden's cancer, though, is not that simple.  But "stable"?  Hell, we'll take "stable."  Here's Handsome Boy:

Handsome Braden, courtesy of his CaringBridge site
 But... as reader TAM and I have commented, back and forth, both of us with the profound luxury of watching only selective truths, and from the comfort of our computers... it is grim with young Joey Keller.
I simply cannot bring myself to bring you up-to-date, if you have chosen to get news of Joey here.  I encourage you to go to his CaringBridge site as the situation is as complex spiritually as it is medically. Bless his parents and their faithful entourage, they cannot let him go... when perhaps, he needs to.  My worst fear is that he may want to, but is so tender-hearted, loves them so much, that he cannot say so, cannot give himself permission, lacking theirs.  This feels cruel to write, and a cold chill of guilt envelops me.  I cannot know or come close to imagining Nick and Elizabeth's tortured pain... but I *do* have a vague idea of Joey's, and that drives my cruel words.

Nick last updated the CaringBridge journal in the very early morning of November 7:


We saw the MRI. Major growth on lumbar spine, brainstem, and in temple regions sort of growing towards the center of his brain. It WAS in CSF kind of "on" his brain, now it seems its growing into and through his actual brain cells and tissue. Wicked, evil disease. We discussed hospice and the reports from all relevant medical teams was, "anything else we could do will cause more harm and damage than any potential for help or therapeutic upside." They do believe his unusually high heart is do to the cancer spot/tumor/lesion on or in his brain stem. We flat out need a miracle. Otherwise, what he will have to endure, systematic loss of brain and organ function, system failure, ventilator again, it's unthinkable. They were especially concerned looking at this MRI vs. the one just a month ago (brain) bc Its really moving quickly. We have got to pray. All those scriptures I looked up and listed in previous CB postings on faith and healing, haven't changed. The promises regarding healing...haven't changed. We've exhausted every medical option that exists (due diligence.) Now, We look to God to do what only He can. All day long I kept thinking about the Israelites looking at the Red Sea, the Egyptians racing to basically cut their throats or put them back into slavery. They thought they were dead. Or at best, had no idea how God would get them out this, this time. Slaves for 400 years, finally free, and now this??? To die here, like this? All day long I've been getting texts from buddies and pastors from those very chapters. Don't believe it's a coincidence. The thought keeps going through my head, if its not impossible, it's not a miracle. Thx for praying for our Joey.
PS- I have been inundated with emails and texts and VM's. thank you all so much for your kind words and for reaching out. I just can't get to them all. In time, I will read and hopefully respond to every one. There are some aspects of my job I must do everyday and outside of that, my time/energy is focused on Joey. I hope you understand. Please, pray. Just pray. Thank you.

Father and Son

Wednesday, September 5, 2012

the one where i finally show my face...

okay, friendly readers, i am wayyyyyy febrile and it's kind of evident.  i hate a sweaty head, in particular, and the shivers.  the burning eyes, not so bad, except that i have made it to then last 20 pages of a novel and now cannot decipher the ending.  maybe by bedtime, which, given that it's now 4 pm, might arrive any time!

here's my plan for this post.  a picture of my hero hannah, as she tests out a prosthesis and remains a young girl staring, unblinking, into big troubles, then flashing a beautifully defiant smile.

then, i am going to try to post a video update of my lovely hands and feet, and maybe a spot from my face, though we all know that'd break the camera, ha ha ha. it's a weird new development, kind of like the weird old bumps and bullae that plague my right leg.  it adds to my feelings of confidence and encourages my desire to appear in public.

as for an update on my relationship with the new specialist on The Team, and my cancellation of the big and important appointment i had with my dear mdvip go-to-guy, i'm gonna lift a "blog" post i put up over at drphil.com, that cess pool of cess pools that attracts me like a cess pool fetishist. oh god.

sometime today, i need to clean our private quarters here in Marlinspike Hall, as Marmy Fluffy Butt has been  experimenting with projectile vomiting -- most impressive, i must say.  thank goodness that our stepdown living room space is populated with most of the mission style furniture put out by l.l. bean -- meaning that slip covers are removable and washable.  not by moi, of course, as this useless left arm is... useless, but by the dear, dear fred.

as for Marmy Fluffy Butt, herself, a large part of the issue, i feel, is that she is still avoiding me like the plague, and i am her main aesthetist.  i was her daily groomer, her weepy eye cleaner.  i kept Miss Thang free of hair balls and other such gross happenings.  however, ever since i administered her eye medicine, she runs from me.

nay, she flees.  it hurts my heart, as that daily time with her was precious and i miss it.

and now, we must worry that she has a gastric blockage, though she did, i believe, just go streaking and shrieking past my bedroom door, Buddy the Freakishly Large Kitten hot on her trail.  so maybe i am worrying needlessly.  but she is such a tiny thing, all hair, really, and she's so weird that i think we may be cosmic twins.

okay, so now that i've exposed the intricate details of this post's plan, i need to go take care of these plebian matters, the vacuuming of the futons, the spot cleaning. oh, and maybe i should begin the makings of a dinner for Fred, and a rapid damp mop of... everywhere.

i cannot tell you how badly i hurt, how much i have cried today.  how hopeless it all seems.  how much martin bashir irritates me.  how i hope michelle obama speaks tonight as we all know she can, and that it lifts my spirits.

msnbc (oh god, don't get me started...) has shown several times a short clip of barbara jordan today, and it has been a comfort, for some reason.  that voice, that dignity, that intelligence.  that humor, and all the unknown suffering turned into triumph simply by who and how she was...

there is hope, there is beauty, there are stolid, solid lovely people.  and i am off to vacuum, dust, and mop -- while the percocet is working.  but i promise to be back to fulfill my compositional promises.

in fact, before i go, here is hannah:

from Hannah's CaringBridge site
this girl rocks.  at the moment, she is getting a break from chemotherapy due to low numbers, not something that anyone wants, though i bet there is a secret bit of relief, a brief sense of vacation.  she's been steadily going through chemo, sometimes clearing her numbers like a champ, sometimes falling prey to fevers and nausea.  but what doesn't change is her steadfast attitude, her straightforward walk through this unexpected trouble.  is she still my hero?  you bet.

okay, i am up and heading for the mission living quarters. yay?
**************************************************************************
it's no longer today, it's tomorrow.
i slept so hard, so long, and am thinking about doing it again.  i missed michello obama's speech. drat.
but i remember the dear ms. keenan, of naral.  hooray!  i think she did a great job.
i have no clear recollection of even writing anything above the dotted line.  still, following my own intructions, i just snapped some photos -- because video is impossible due to my hands shaking.

first, five photos of my right foot, the site of onset for "my" CRPS.  i think i will eventually lose that leg.  this is the leg that the new superduper famous ortho i saw last week would not even look at. not a brave soul, him. he?

then comes the most painful, though not the most painful looking -- my left foot/leg.  only two shots because the pain just does not show.  the onset of CRPS in the left leg came about 2 years after the right foot/leg.  i simply woke one morning, and *poof* -- there it was, a purple, cold, burning left foot.  and now, this foot/leg is behind most of my extremely loud, hopeless verbalizations and castigations of God.

next... my hands are kind of freaky right now, and embarrassing... so i just showed you the extreme weirdness of the nails.  it began on my left hand a couple of years ago -- the thumb and middle finger only.  then, one morning -- *poof* -- i noticed that the thumb and middle finger of my *right* hand had begun to ape the left side.  the symmetry of CRPS is just... creepy.

i had to show you poor marmy, hiding away.  she's upset that we washed and vacuumed and generally rendered antiseptic her favorite furniture, plus she feels like crap and won't accept any nuggles or loving.  i did see her scarf down a few treats though, so she's okay...

also, marmy is there as a buffer for the first time i've ever shown even a bit of my face.  maybe now my family, constantly demanding photos of "me" can understand.  i have CRPS crapola even on my face.  please respect how absolutely ugly and socially WRONG that makes me feel.

besides, you know the rule:  no wearing of CRPS faces out-of-doors or in photography/videography after labor day.

without further ado:














oops, i almost forgot the cess pool of cess pools, the "community blog" area of drphil dot com.  why i put it there is anyone's guess.  oh, i know:  i think dr. phil can cure me.  i think he is one hunk of a brilliant psychologist.  yeah, that was it.  so here it is.  stylistic differences and lack of cussing that may be of note are due to an ongoing war with moderators there, who do not like publishing ANYTHING i write.  hmmm, maybe that is why i am over there, pelleting them with writing!


summing up  [stolen from drphil.com, mwa ha ha ha!]
i have to redefine my relationship with my "mdvip go-to-guy," my pseudo-concierge internist who has been keeping me alive for about 13 years now.  i cancelled a huge appointment i had set up with him for tuesday after my experience with the new ortho specialist i saw last week.

basically, the hip dude (as we shall call the new specialist) said he would be "too scared" and even "terrified" to operate -- and he's purportedly one of the top hip dudes in the country.  he looked mostly at the floor while he talked to me.  he had already spoken -- twice -- to my infectious disease dood guy, and, to shoulderman, as well.  he did not even want to proceed with a simple ultrasound, and really, really wanted to avoid discussing doing an aspiration under fluoroscopy.

i drove him to his bottom line and that turned out to be... no one thinks even a wash out of the right hip is worth doing.  they don't think any more effort should be expended on trying to defeat this infection.

i pointed out, with what i consider amazing calm, that this leaves me with daily fevers, chills, sweats, whole days in bed, whole weeks in bed, and diminished.... everything.  i did not mention pain, because then my sangfroid would have boiled over.  i did not mention pain because, hey!  that wasn't his specialty.

i tried to poke at him enough to see if the CRPS in that leg, in particular, was part of his reluctance to go after the infection.  just as he wouldn't look at me, he wouldn't look at that leg.

so... i am to keep a follow-up appointment with infectious disease dood, even though that appointment does not exist.  i am to wait another month, for a reason i cannot remember -- but i think he wants more time between ending abx and testing.

but then, what to do with the message:  if we grow a pathogen from the aspiration, i still won't operate?

so i came home, crying in the car, because, damn it, it hurt -- and then looked at the calendar and  saw my upcoming big assessment appointment with mdvip go-to-guy.... and emailed him to cancel.  he's been very brave, very helpful... but if the specialists won't do any more, what can he?

my last visit with nathalie, i begged for an injection of toradol.  she said they didn't have any.... "sorry." so when we were in the pharmacy, filling all the damn opiate prescriptions, i pulled the dear pharmacist aside and asked him if toradol was available in non-injection form.  "yeah, and i don't know why, but no one prescribes it anymore except as inpatient, by i.v...." so i ran (okay, rode) back up to the office, and left a note marked URGENT for nathalie... and lo!  the angel of the lord guided her hand and mind, and she called down a 5 day prescription.  it's a pretty dangerous drug, and that's as long as i can have it.  so this is my first whole 24 hours off and i can feel it.  will she let me have it one week out of the month, do you thnk?  one week when the bone pain can be brought down to non-screaming levels?

go-to-guy doesn't know this happened, nor shoulderman.  i've had serious bleeds in the past and all that jazz, my hemoglobin is dropping about a point a week (until i stopped going in to have it drawn) -- "for some reason."

i feel like i need to tell fred that i've reached the end... the trouble is, he thinks i've been there so many times before, he won't pay attention, or he'll think it is the pain talking.  i had hoped to leave him more money and a more organized house (one that could practically run itself!) -- but i have done the best i can.

so i am blowing off all the specialty dudes, and even my dear mdvip go-to-guy, though i know he is there for me, and always will be.  god bless the man.  this is how he answered my email:  "Sorry for what you're having to go through. I wish there's more I could do to help you."

and that about sums it up, eh?

Saturday, June 30, 2012

Why I Cannot Commit Suicide

I'm a mess.  There are things to do about it, and I'm working my way to and through them.

On one level, oh Sweet Lord, I want a shower.  To this there are challenges and warnings, but I have faith in Saran Wrap, paper tape, a portable shower head, and a growing "who cares" attitude that is building up a head of steam. The lower part of the incision is doing its gravitational obéissance and leaking, and then there is the whole no shoulder thing.

On another level, but really pretty perpendicular, or lateral, or... the same, I need to figure a way to stop this eating in my sleep business.  Waking with a spoon laden with Carbsense Peach yogurt kind of latched onto your pajama top is... well, hell, we've reached the point of BORING.  No marinara sauce, no sushi, no chocolate oatmeal (my *waking* favorite meal of the moment).  Just weirdly gelled and separated Carbsense Peach yogurt, neatly spooned, and attached mid-boobies.

Other messes are harder.  Like, if I keep giving away all my love and possessions, do I have to fit the suicidal paradigm?

If Fred actually helps me with the budget for 2012, and yes, I DO know that it's essentially JULY, does that mean anything?  And if he doesn't, and I stick to my threatened ultimatum of arbitrarily assigning weighted financial responsibilities according to my guilt-driven whims, does he really hate me that much?

If Marmy doesn't overcome her resentment of my treatment of her herpes infected eyeballs, I may just melt into nothingness.  She wants me;  I want her -- yet all we can accomplish are mutual sexy eye winks and finger-nose kisses.  She has this thing where she loves no one but the boy cats from around 5 AM to noon, when serious sleeping commences for her, them, and most of the inhabitants of Marlinspike Hall, the Haddock family's ancestral home.  If you've not heard of the Haddocks and cannot locate Tête de Hergé on MapQuest, don't feel bad -- the world is getting bigger every day, and we're just in another part of it.
Anyway, Marmy Fluffy Butt *will* socialize with humans after 5 PM, but only in one room, and only when she is standing on the floor, ready and able to make a run for it.  Around 10 PM, she's a delightfully uncomplicated creature, who will do the flop and let you play with her warm belly.  Anyone at all can pick her up, love on her, be utterly silly with her and have her trill-and-twirl her way right into their hearts... except for moi.  I get a clear hiss and a glimpse, plus a whiff, of the tartar and tooth decay we have to highjack her to the vet for next.

She's no fool.  She's seen three of her dearest friends go off to the vet and not return.  So when I bring my supplies to treat her funky eye, and those supplies still smell of vet smells, I am not to be trusted.

Dobby is still with me, though he grieves.  I am crying too much, too much the fool, and losing my focus.  The focus should be Dobby's derrière, it's need for a light and deft whacking.  Every encounter requires a few minutes of brushing, as well.  Buddy the Freakishly Large Kitten has no messes (beyond hairballs -- he's a Maine Coon who abhors being brushed) except for a small daily requirement of pounds and pounds of bonito flakes.

Messes?  I guess not, not really.  These probably fit the bill better:

Why turn the page of a mediocre novel?
Who cares if you need more pain medication?
Thanking a person is nothing.  Showing by some sort of doing, that's the ticket.  But how do you get out of the crap of this tit-for-tat nonsense?  How are you, you, trapped in that tit-tat nonsense more than anyone, not hurt when there's no light in the eye, back?  There's no spark of memory, recognition, nothing?
What's the answer to "How are you able to sustain such good spirits?"
I've had a strong and very compelling urge to drink -- single malt whiskey only.  Sudden, strong, compelling, and always ignored.  I don't drink.

I have a mess with the IRS, or will, if I don't file soon.  See, I don't *need* to file... don't owe, nothing of that sort.  But I have crap to report and haven't taken the blessed 5 minutes to do it.

The surgery I need on my eyes, that I've just been putting off until the Shoulder Saga ended, hahahahahaha, has become messy because Propionibacterium acnes is one of the more horrid complications.  When I see the good eye doctor again, she will likely laugh at this mess I've built in my mind from reading the silly interwebs.

I am switching from the very small amount of methadone that I was on (15 mg/day) to fentanyl patches.  But I forgot about tapering down the methadone and just switched.  I cannot count the number of eyes that I've watched roll and loop-the-loop when I launch into "My Mess" speech after hearing that.

Am I a lumbering pharmaceutical?  Am I my WBC count, my sed rate, my CRP?

There is no one to whom I want to give the beautiful gold jade-y and celadon-y green red ruby earrings that R brought me from Iran.  What a pisser of a reason to have to stay alive, that I don't wear gold.  I wear silver.  That doesn't impact on the giving-them-away part of things, except to say that figuring their weight in love is complicated by lack of use.  And thus, I am saved, left to my messes.*






* And my alegiance, no joke, to the courage of Hannah.

Wednesday, June 13, 2012

Okie-Dokie, Then!

I don't know how to describe yesterday, except to say that, during the night, evidence suggests that I ate a bag of microwave popcorn, one and a half apples, and a "carbsense" peach yogurt.  The evidence comes in the form of popcorn kernels all over the floor, one well-gnawed apple core, one apple sliced neatly in half -- brown but with that still (barely) good nutty apple smell -- smartly speared with a small utility knife, and an upside down carbsense peach yogurt balanced on the pillow I was hugging with wanton abandon.  A spoon smeared with yogurt sat neatly upon my carefully folded glasses.

In further riotous detail -- I woke hypoglycemic.

Back to yesterday, which shall absorb the blame and the shame for all of these disgusting nighttime activities.

I know that I apologized to my President, Mr. Obama, several times, even, on Twitter, for singlehandedly destroying the PCIP budget.

[ASIDE:  Please, MSNBC, among the many programmatic and philosophical changes you need to make, do not force Luke Russert upon us.]

As I was saying, I may have annihilated the Affordable Care Act all by my lonesome, just by the shenanigans of January and February, in our upteenth attempt to rid my body of an osteomyelitis that just won't quit.  Transfer to a Long Term Acute Care Facility was involved, as were superfluous surgeries, and massive failure to understand the machinations of CRPS / RSD.  One of the results of all the money thrown at my problems was the declaration that I had maxed out my PCIP coverage to the tune of.... "catastrophic" levels.  My main comment on that is that the maximum I was told I'd have to spend on my health care (not including, of course, premium costs and deductibles) was roughly $7,000.  Excuse me while I imitate someone doubled over in laughter.

So one of the joyous benefits of having been hit so hard financially in the space of the first two months of the coverage year is that I am exempt from paying any more co-pays for doctor visits, etc.  I am at that glorious 100% coverage realm, up where the air is so thin, one can hardly breathe.

And yet, every doctor's office that I visit demands that $25 or, at one place, that $55, before I can be seen.  Never mind that I've been with each of them for years and never, ever carry a balance.  (JOKE:  I'd rather die first!)  Now, this is the true me:  For a couple of weeks, I was just so tired, I said, "Okie-dokie, then, here you go!" 

Then I had the fire lit under my aching, red, and breaking-down butt.  It turned out that my orthopedic surgeon's office had NOT applied to my PCIP deductible the $2000 I put on my credit card when they called on January 17, 2012, claiming I needed to pay them the in-network deductible or they'd be unable to proceed with the grand screw-up of a surgery scheduled for January 23.  Did you follow that?  I could make it clearer, but I'm so stuffed with food I can barely think.

As I was investigating a weird charge from the LTAC, submitted by a pulmonologist I'd never heard of, nor needed, who also appeared to have no license in this area West of the Lone Alp... I became mired in the pages and pages of online data documenting the obscene, pornographic exchanges of money, it hit me that I could not find that $2000 payment from January.  

I can be quite the dip when it comes to money, so I thought a courtesy call to the orthopod's office was in order before I set my aching, red, broken-down butt afire.  Anyway... no, they had only "needed" about $200 of all that, and had just tucked the rest in between the brown corduroy orthopedic sofa cushions in their snack lounge.  Miss Melissa, after sternly reminding me that she had only known of the error since March, eventually returned the $1700+ to my credit card.

I had to jump up and down over and over on the radio that kept playing in my head:  "And what about the interest charges you incurred, nimwit?  What about the money you might have grown from that $1700+ had you been able to invest it in the equity that went up over 23% in that same period of time?"  Smashed that damned radio to pieces, I did.

So yesterday, Fred and I sat in the waiting room at ShoulderMan's office, discussing some hilarious scientific literature. [Not kidding!  He was showing me the studies proving that light, among all observable things, changes its behavior if... observed.  Hilarious and mind-boggling stuff that makes me believe in God even more than that rare child cured of persnickety and metastatic brain cancer.  Fred can be a brilliant man, knowing when to pull out the big guns.]  

Now, I already may have pissed one of the receptionists off, I am not sure.  I was trying to be helpful, but how often does "trying to be helpful" really mean "pointing out crap that no one wants to deal with, and thankyouverymuch."  All of these orthopods have installed "kiosks" for check-in purposes.  It scans your IDs, your insurance cards, updates your address and phone, and asks whether you're likely to vote for President Obama or Dickwad Romney.  Oh, and please press HERE if you are not white.

I always complain about these kiosks.  Several reasons:  I am in a wheelchair, and the slant of the screen makes it nearly impossible to read due to glare from the sun -- that sun that may emit particles or waves, but probably isn't a coherent light source, anyway, who knows?  I ask them for a lower kiosk, as well.  Think about it.  I am in a wheelchair.  The kiosk is raised for someone of normal height, standing.  And why am I there?  Because of my freaking shoulders.  There's something so not fun about having one barely working arm that you have to keep raising above your head to enter data that hasn't changed since the week before.

Ah, but none of those bitchifications were involved in my complaint yesterday.  When I rolled up to the kiosk, it had been left by its previous victim in mid-operation.  I silently acknowledged my agreement with the evidence of their frustration, briefly bowing my head, and saying my personal and shortened version of the Serenity Prayer.  There was no way to abort the half-finished session, so I just flew through each screen by pushing some version of "Don't Know" and "Don't Care." The last screen I saw, still dedicated to this long gone patient, offered me EVERY SINGLE BIT OF THEIR PERSONAL INFORMATION.  From social security number to address, phone, personal doctor's name, insurance data -- all of it.  I could have copied it all down, photographed it, or I could have gone slightly bonkers and rolled over to the receptionist to report what I thought a major flaw with their blessed little kiosks.  She said, "Oh, no, that's terrible." 

I shortened the Shortened Serenity Prayer and went back to the kiosk to enter my own data.

Fred and I resumed giggling over the double slit experiment.  ("In 2002, Jónsson's double-slit experiment was voted 'the most beautiful experiment' by readers of Physics World.")  I was waiting for my main man, Leo, ShoulderMan's left hand man, to call me back to the exam rooms, when instead I heard the receptionist's dulcet tones, asking me to report to her area.  Zoom, zoom, zoom, and there I was -- hidden, of course, behind the counter that was so tall someone in a wheelchair would never be noticed without use of an emergency flare.  

She has two things to accomplish.  One, could I please confirm the information I just scanned and entered into the goddamned kiosk.  Two, I owe a $25 copay.  I am already missing Fred and his promise of some mention of Schrodinger's cat.  I carefully repeat the necessary demographics, but balk at paying.  My chapped ass has had enough, already.

"Well," she said, between huge sighs, "I guess I can call and reverify your insurance coverage." 

"Okie-dokie, then!" I crow.

"You can stay right there, so you don't have to go running back and forth."

"Okie-dokie!" (Appreciative of her saving my thumb and forefinger all that effort...)

Twenty minutes later, I am the source of major human traffic flow complictions.  My wheelchair is blocking old men with walkers, little girls struggling with crutches, and various blue-hairs who just shoot me a dirty look before lining up behind me, despite my frequent announcements that I am not in line.

Every now and then, the receptionist says something in a loud voice and I've no idea if she is speaking to me, so I answer, even if at the "okie-dokie" level.  Occasionally, she says, "I'm so sorry!" and it is then obviously incumbent upon me to say, "You've got nothing to be sorry about."  Oh, how weird things get when you cannot see the person with whom you might be having a conversation.

Finally, I hear this:  "Oh, you're gonna hate to hear this, Ms. Profderien!  You are absolutely right. You don't owe us a thing.  You can take a seat now."

You'd have been proud of me.  "[cough::cough]  I don't suppose you could refund the $25 I had to pay last week...?"  And then I rolled my aching, red, broken-down butt to Fred, who was asleep under a book, snoring just the smallest bit.  He woke, thought I had already seen the doctor, and make ready to leave, cheerful at the well-oiled machine that was apparently in force.  I hated to break it to him -- we had yet to really begin.

The chase?  You want me to cut to the chase?  Okay... Leo called me back, told the same joke he always tells, the Nurse Who Really Runs Everything came in and I signed all the consents, and we looked at my blood work.  She kept saying, "Your CRP is *really* high..." After running back and forth to consult with the surgeon, she decided I needed to be the last case of the day next Monday, because odds are that there is more crapalaficious infection to be dealt with, and "the infecteds" are always operated on last in the surgical day.  She sends in the PA who says, "You know the drill," and then seems to fall into a fugue state.  "Bob," I said, "You seem really tired.  Why don't we just move all this along?" Bob seems grateful and says I need to "run" across the street to the hospital to pre-register.




Before I leave, I pick up all the paperwork (including the blood work results) that have fallen on the floor, and stealthily crept under the exam table.  I leave them in a place that's obvious, so that either the next patient can steal my personal data, or the Nurse Who Really Runs Everything can retrieve them, so as to fatten up my anorexic chart (we're on overstuffed Volume 3).

We did not know that hospital pre-registration was going to have to be done yesterday but Fred and I decide to see it as a good thing, meaning that we don't have to come back later this week, and can stay home waiting for the roofing dude to come save the collapsing roof over one of the rear porches overlooking the fruit orchard we share with our Cistercian neighbors.  Believe it or not, the whole thing sort of collapsed 5 days before the 5-year warrranty expired on the last time they came and did not repair it very well.  If there are any charges to come out of this repair, you can bet that we're inviting Abbot Truffatore over for dinner, al fresco, with his seat right under the most prodigious leak.

I pay the $5 for parking so that we can go park at the hospital, which will cost -- you guessed it! -- an additional $5.  Fred threatens to muzzle me as I launch into my "Dear President Obama..." routine.  Why try to save me with an Affordable Care Act and then bankrupt me with health care parking fees?

Anyway, we know this hospital like some people might know the back of their hands.  But right away, something is different.  I am in a cubicle with a polite young man who is reentering all that personal data stuff, when he pauses, actually stops working, and says, "Do you mind if I ask you a question?" 

Oh, what goes through one's mind.  "Yes, I know I still owe you many thousands of dollars.  I'm sorry.  If Google would just have a blow out of an earnings report, you'll be paid that much quicker.  In the mean time, would you accept $20 a month, or maybe a kidney?" 

But what he asks is this:  "Was your experience here back in January and February a good one?"

I think I swallowed my tongue.  "No," I said, "it wasn't." 

"Well, I am sorry about that, and I hope that from this moment on, your stay here this time will be much better."

I am tempted to yell out "WTF?" but don't.

Okay, so I got a Press Ganey thingy to fill out on the hospital, back in March, and filled it out with bloody honesty, but how the heck would he know anything about that?  And he is, no offense, just a data entry clerk.  And wasn't it anonymous?

I'll spare you.  The tenor of his overtly solicitous behavior continued throughout the pre-op check-in process.  The nurse was extremely polite and well-informed.  She knew what CRPS was.  She had an accurate list of my meds.  She listened as I begged for them not to change the marvel of the pharmaceutical arrangement that is helping me so much with the CRPS dystonia.  She did not make me repeat tests that had been done within the last six months.

She passed me along to the nurse anesthetist whom I absolutely HATE.  I am sorry to say that.  Ashamed to say that.  But this woman, every darned time, interrupts me when I bring up the need for stress-dose steroids pre-, intra-, and post- op... and then to please revert me to my normal dose.  She lectures me on the hospital's pristine record with steroids, given that it is one of the region's foremost transplant centers and blah blah blah.  This time, I talked over her, telling her that I was very nearly dead thanks to their own hospitalist not givng me ANY steroid for five days, while I became more and more altered, with systems failing, getting weaker and weaker, and no one sharp enough to check my medic alert tag, or even look at the hospital records from an admission a mere two weeks before.  "Oh, my," she says.  "That should not have happened.  I'm so glad we discovered it in time." 

Scrape me off the ceiling.

I tell her that I discovered it.  It probably would have been my last cogent comment. Vision fading, weakness rising, I asked the nurse who was giving me meds which one of all those white pills was my steroid.  She told me I didn't take steroids.  I believe I began blubbering "Oh, my God, oh my God." To this good nurse's credit, she RAN to get help -- and a syringe full of Solu-Cortef.

Anyway... we got through yesterday, I hyperfocused on the weirdness, and then we got a pizza, for comfort.  It was after 7 pm before Ruby the Honda CRV rolled gently through the labyrinth, among the ramparts and over the moats, drawbridges and cleverly converted battering rams, into the safety of the well-loved place called home.

I have not forgotten young Hannah, to whom I promised to look for inspiration in all this -- but I cannot think much about how mutilated I will be when I come out of anesthesia on Monday.  Later today, I will check on her progress, and again marvel at her strength, and pray to be able to imitate her just a bit, if nothing else.  She is doing well, I know, midst a sucky situation.  She's been fitted for a prosthetic leg and will soon begin learning how to use it -- which I expect will take her a full five minutes.  Keep on keeping on, Miss Hannah.