In Pre-Op |
Never ever did I imagine my life would take me on this
journey…All my life, I have wanted to work with children with disabilities…but
never did I think I would have children with disability…I have dreamed of
becoming a mother…but never did I believe I would be the mother of two children
with chronic illness. I have hoped to
marry a loving, caring husband, but never could I imagine I would partner with
the most amazing individual with incredible amounts of love and he shares it
all with me and our two beautiful boys; and still he has love to spare.
Some days my brain feels like its on overload. Today is one of those days. Mixed feelings fill my heart, giving me a
sense of emotions-on-overdrive…I just went from tough mean-mommy, to having a
sense of stabbing sadness of what Parker has to endure if he wants to
walk, to my heart breaking knowing that he is telling us (PT, nurse and me) the
complete truth that he hurts so very bad, to knowing I must muster up that
tough love and MAKE him do what he doesn’t want to do because he knows it will
cause more and more pain… I had to make
him put those arms with flaring shoulders and wrists down and wiggle and scoot
and drag those million-pound legs/feet and lift himself into his
wheelchair. Then the torture continued
as we had to then get those legs off that bed and down onto the wheelchair foot
rest as tears rolled down his face and “I hate you all” came out of his mouth…But…
the one emotion that is emerging more than all the rest is incredible pride in
the strength and bravery that Parker is enduring this…because he DID it, he
really DID it with splints on his legs/feet, cadaver bones piecing him back
together in alignment, and pins criss-crossing through his bones holding it all
together and in place.
I know there are many adults with RA that have had
reconstruction…but we only know a few kiddos who have endured some sort of
reconstructive surgery. WOWZERS! I am so incredibly amazed with each and every
one of those kid-heroes. What they have
accomplished is a miracle. I just watched
my kiddo go from hating us to just about doing the entire transfer back into
bed, with such determination, that he did most of it with his own strength and
not one complaint. The nurse was
shocked!
Gram & Gramp |
This hospital does not have pediatric rheumatologist; and
so the medical staff rarely work with kids with juvenile arthritis. So, to have a kid like Parker and all his
complexity…well, let’s just say, that all have learned a ton this past week and
they have been absolutely open to learning.
I actually really appreciate their interest and questions, verses just
pretending that they “know”. It is very
refreshing and Parker feels really smart as he educates them.
So if you are reading all this…YOU are one of those
really special people who care a whole lot.
We so appreciate all the out-pour of love, support and prayers we have
received this week. It truly has powered
our entire family and we really needed it.
Many of you have asked how you can help…there are two ways you can help both
us and children with JA. One, our whole
family is very involved with the National JA Conference this year because it is
being hosted in Florida. If you know a
potential donor, in-kind sponsor, or you would like to volunteer with either
prep or at the conference event, please contact us or Susan Cuellar (Florida AF
office: 813-968-7000 or 1-800-850-9455
x11) and tell her you know us and how you would like to help. And two, as you
may know, the walk will be this May and we would love for you to sign-up (it is
free) and walk alongside our family on “Parker’s Purple Playas and Logan’s
Dream Team”. (Click here to sign up on our team.) And of course, we also welcome
donations to our walk team, too because we definitely need more research
towards a cure, to send kids to camp, and to scholarship families to go to
conference.
Like I said, never did I imagine that my life would take
me on this journey…but it has and I am proud to say that I have become a nurse,
a fundraiser, a conference planner, a JA educator, a counselor, a motivator,
but most importantly…I am a wife and a mother who deeply loves my family and am
so happy that there are people like you in our lives who love us too.
Parker's first post-op request was to see his brother, Logan. |
Parker is a super hero in a family of heroes! We continue to keep you lifted up in prayer. Love always, Cathy and Dave Stone
ReplyDeleteThank you Cathy and Dave. We hope to see you and your dogs out at the walk again this year. We miss you.
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