Sunday, November 13, 2011

PS

...To the meds coverage story.  I did it.  The pharmacist was surprised, and she said so, but I did it:  Q has the Prevacid prescription and it filled.  The pediatrician wrote it for "ONE YEAR," "dispense as written; patient has swallowing difficulty" and it went through.  We'll see what happens when we hit the 90-day mark and the state wants to have this conversation again. 

Next step?  To get a response from the state for the pharmacy corporate office with regards to refunding my out of pocket expenses.  Prayers over this would be appreciated.  I will get this done, too, but (whispering) I'm a little tired...  At this point, we could use that refund (we're out of eggs) and this thing needs to resolve this week because I have the next level of things to move on.  No time for lollygagging, dontcha know! 

In the meantime, I'm going to go sleep so I can be all bright-eyed and make more applesauce and apple butter tomorrow.  Ooo - maybe some pear sauce, too.  Cheap fruit = good, cheap food.  Wheee!

Thursday, November 10, 2011

Good life

Such a lot of water under the bridge(s)! 

Let's talk about Mr.Q first.  He's has been sleeping... well, not great over the last couple of weeks, resulting in new local peaks in pharmaceutical caffeine use (by moi).  The rehab visit went well, but I'm having trouble wrapping my head around the A & P aspects of the selective dorsal rhizotomy discussion.  It would seem that new, more delicate techniques and growing experience in neurosurgery are allowing kids who have inappropriate lower limb tone to benefit quite nicely from a procedure for which they would not have previously been candidates.  Hooray!  So perhaps that would be an alternative to the Baclofen pump.  The thing is, every time Q's Baclofen dosing has increased, so has his swallowing ability, vocalization, overall healthy muscle tone and mass - all of these are huge.  Just huge for him.  So at this point, I'd want to go ahead with the Baclofen pump at some point, even if there would be excellent gains to be made in the rhizotomy - Q needs those upper trunk and extremities benefits.  I think that's part of why he hasn't had any remarkable respiratory events (requiring steroids of any kind or breathing treatments) in almost two years.

But back to that "rhizotomy" word.  I usually take in all the info for these appointments, go make notes, read whatever reports that are sent, synthesize with other things I know about Q, and on we go.  But that word...  It means "to sever nerve roots in the spinal cord."  I just kept looking at his little back, then at the drawing on the white board, showing how certain little roots get clipped and where.  His skin is all soft and unmarked there...  I do get that the hip surgery and a possible placement of a pump also require incisions into that perfect little skin.  There's just something about this procedure that seems somehow worse.  As if there's a hierarchy for incisions...  I still have that spot picked out in the backyard.  For puking. Which doesn't seem at all theoretical to me...

Q had two evals on the same day with the OT/PT pump placement team.  I don't have reports from them yet, but I expect them to say that a pump would be appropriate when Q's tone has reached the point that we feel life is unworkable here.  He's tighter now than he was a few months ago, despite PT, massage, stretching, and Baclofen.  So dressing is tougher, as well as arranging him for sleep, transfers for bathing, feeding, etc.  As much as he wants to help, there are definitely certain losses in progress.  He is more volitional or intentional (both?) about his own position - working to hold himself up in his chair before he's completely buckled or strapped in,  holding up his hands for dressing or undressing (and laughing like mad as his fists emerge from the sleeves), lifting his pelvis for pants or changing.  He's working more purposefully, but he's tighter as he does so, if that makes sense.  All things to consider.

I know there's more, but I need to sleeeeeeep (whine).  We're running  four days a week as we train for a December 5K.  The girls are noticing their muscles are different, which has provided neat segues into conversations about body image, confidence, and how to be the best person we can each be (vs. "fitting in" and trying to be like someone else).  We've also got the usual subjects on deck for school, plus it's been fun to discover that Q is studying a little medieval history in his kindergarten class while his sisters are digging into it  at home.  G is finding his feet at high school - discovering the need for hard work in addition to good test scores.  And what a lesson to apply throughout life:  one must show up for and complete the difficult things as well as the fun or easy.  (insert eyebrow waggle)   In the meantime, he's enjoying after school activities and hanging out with neighborhood friends, though his mother wishes he had more homework because kids these days need to work harder!!  (Heh.)

So because of the above, I've got to get to sleep.  My syntax is suffering.  And since I've just poured lemon ginger tea down my shirt...  G'night. 

Wednesday, November 09, 2011

Whoosh

This is amazing.  Transcendent, I think...

Saturday, October 29, 2011

Wednesday, October 26, 2011

Spot on

Sissy Free Task.  Indeed.

Since I'm here...  The ongoing prescription argument is frustrating.  Q needs the solutab.  We've tried the liquid proton pump inhibitor (neurological side effects), Prilosec OTC (didn't work).  He can't take Zantac, because it's in capsule form.  There are little packets of soluble powder that could be mixed with sugar water, but that's omeprazole, the same med as Prilosec, which didn't work.  Meanwhile, there's no word that the paperwork is getting where it needs to go, and the manufacturers have either stopped making the med permanently or have been on backorder since June.  There are non-generic solutabs available, for which I will still be paying out of pocket, but instead of almost $6 each, it's more like $10.  So.  As soon as Q is on the bus in the morning, and just before the girls and I sit down to contemplate the birth of astrophysics, fractions and variables, predicate nominatives, and the medieval-era invasion of Islam, I will make the rounds again on the phone.  I shall strive to be...  Well.  Let's aim for patient, shall we?  I first began this conversation in May, so I think the bar of patience is plenty high.  I do have the phone numbers of all my state reps, and maaaan...  I'm considering using them.

Time for sleep.  Peace out.

Wednesday, September 07, 2011

Info.

Our church seems to be preparing for ongoing conversations about mental health issues.  While thinking about this and some events that have led up to this, I've been reading about and ruminating on a few diagnoses.  It's pretty fascinating stuff.  As difficult as the subject matter can be, especially when families are suffering, remaining blissfully ignorant isn't really an option.  Knowledge is power and ought to help us better understand ourselves and the people we love.  Here are a few links.

Borderline Personality Disorder
Major Depression
Beyond Blue - a very useful blog
Amen Clinics - brain care and brain health, started by Dr. Daniel Amen
Traumatic Brain Injury - MedlinePlus, with links to other pages
Traumatic Brain Injury - Wikipedia, with more detail, discussion of current grading techniques, etc.

If you have good resources please share!  Pax.

Tuesday, August 16, 2011

Onward

We're now in the middle of the week in which we do our church's version of VBS - with dinner served and lots of cool projects.  So much fun!   G and E are serving as "table captains" which is sort of like a camp counselor role to the other kids.  E has a table of four little girls and they're all doing these projects together.  So stinking cute!

The director for our camp last week gave me a jar of dahlias Monday evening and thanked me for bringing Q to camp.  I cried.  She told me that there were so many faculty and staff, and other parents, who commented on our neat family dynamic and what an amazing job the bigger kids did with Q - especially when we were seated on the front rows for the concerts and Q was loving all that live music, and wiggling like a boy who'd been sitting still too long.  I hugged her and cried.  How incredibly kind of her to have taken the time and acknowledged both the beauty and the difficulty in one fell swoop.  It is both.  Always both.  But the former far outweighs the latter, in sheer mass.

And speaking of all that Life business...  You know, I've given up a lot of thoughts about what constitutes an "ideal" family.  I was somewhat surprised to discover, rather recently, that I really do still miss the partnerships to be found in a good marriage.  Even a barely civil marriage provides certain benefits to the spouses, most of them simply logistical.  But even in a just better than barely civil marriage, those losses begin to be keenly felt.  Imagine how lovely it would be to know that the end result of one's hashing things out with one's kid didn't then rest solely on one set of shoulders.  Support in or for one's ideas is sweet, and deserves to be treasured for the gift that it is, of course.  But nothing replaces that other parent "having your back," you know?  In all those small but important ways.

Hope you're resting well and got to spy some meteors this week!  Godspeed, lovely people.