Chloe's symptoms and/or concerns include:When I put all this together in a nice neat little chart I looked up every word in her 150+ page medical records that I did not know the meaning too. I took notes and I became familiar with her whole chart. Upon looking up different words I happened upon a site that mentioned a thing called "Happy Puppet Syndrome" I looked it up out of curiosity, but low and behold I discovered that it fit Chloe as if it had been written about her. Texting my doctor I asked if I was crazy for even thinking this might be it. He didn't think I was. Hoping I was wrong I waited the two days and then on friday morning I brought it up to the genetisit. I despratly wanted him to run the tests to appease me but to say that it was more likely this that or another that wasn't so bad, I mean this is a RARE syndrome. VERY VERY rare, like crazy Mystery Diagnosis rare. And as we ALL know rare only happens to other people right? After looking her over and spending an hour asking me all kinds of questions he said that he didn't want to waste time or money testing things he didn't think it was so he would only test for one thing. Angelman Syndrome. aka Happy Puppet Syndrome. About two hours after walking out of the mans office the enormity of the situation hit me and had it not been for a dear friend I am sure I would have been crushed by it. We are now going to have an MRI and a EEG done along with another Chromosome test. the MRI and EEG (both are to be done with Chloe put to sleep) will be done sometime next week or the week after. I feel that if the EEG comes back abnormal then that is my conformation that it is. I would give anything for this not to be what she has. I want so badly to wake up tomorrow and her to talk and walk and act like any other toddler her age. I want to see her in her pretty pink tu-tu twirling around awkwardly at her first dance recital. I want to hear her tell me about her friends and her hopes and fears. but I know... this is not going to happen. God could heal her, He spoke the world into existance but he wont heal her. I'm not mad at him. I know that he knows more about this whole thing than I do. I know that he is in control and that ultimatly he will be glorified in this. I know this, I don't like it. I don't like that He CAN do something but he won't, but I'm not mad. I'm just sad. So very very very sad. I have cried no stop since Friday. really. I have already gone through two brnad new sets of contacts. I eat because its time to eat not becauce i'm hungry, I go to bed when its time to go to bed but I dont sleep (unless Bobby gives me a nifty pill to hlep me sleep)to say I'm an emotional wreck would a this point be an understatment. Everyone says that I need to wait to get the test results. But see I think of this as my mourning time, and when the results come back it's time to kick it into gear and make the million calls to the medicaid disability office, the social security people. the therepists, the million other people I need to contact to get Chloe the best possible help and all thing things she is going to need, we are going to have to think about education options and long term care options. We are going to need to look into either handicapping our hoome or look into finding the funding to get a house that is larger that can accomidate her and the the equipment she is going to need and the resourses that she is going to need. A bigger house with more handicap features would be nice. Heck a house with a second bathroom and with out mold or structural issues would be nice. but the point is right now I can mourn the loss of the dreams I had for her, the prom and wedding dreams, the ballet and crummy art project dreams, the dream of she and I in our kitchen with little matching aprons making thinksgiving dinner for everyone. The dream of her holding her daughter and letting me kiss my granddaughter The million other little dreams you have that you don't know you have. In an instant all that is gone, and it is replaced with adult diapers, infant toys at 20 and an infants mindset in a ever growing body, Now is my time to lose it because later I will be too busy,Everyone has asked what they can do and I have really had no idea, I;m really not thinking all that clearly. but I have thought of some things and just not had the gumption to really say what is it that I need, but here on my blog in my own little world, here where I am convinced no one will ever read I can tell you. because you aren't real. I need prayer... lots and lots of prayer. Mostly Prayer that either she will be healed or that she doesn't even have it. I need you to look up what Angelman is yourself because for me to tell you is hearbreaking and for you not to know is heartbreaking. I need my house cleaned and I need my laundry done. I was behind in housework before being a homeschool mom of three littleer ones but now... yeah it's bad... I mean like the begining stages of hoarders bad. A clean house always makes me feel better and it lifts my spirits but right now I can't. And prayer, I can't get enough prayer. WOW I sound pathetic. but yeah that's about how it goes. I have never been so low. So that is why I haven't been blogging. Just in case you wondered
(3/22/11) Congenital Miscrocephalus (present since birth)
Failure to Thrive (present since birth)
PAC's
Esotropia
Hypoglycemic
Tremors (ongoing) Physical Therapist said they appear to be attention tremors
but that they are also intermittently over all her body
gross low global tone (ongoing)
planter grasp reflex with curling of toes (noted on 2/04/11)
Toe hallux valgus right is worse than left (noted on 2/04/11)
Peabody Developmental Motor Scale of 32 for stationary (9 months) and locomotion raw score of 38 (7 months) (noted on 2/04/11)
arm flapping (on going)
one word spoken "Mama" used intermittently (never used with eye contact to me her mother)
little outside babbling
first smile one day after birth
first clicking noise 2 weeks after birth
has pulled up twice unassisted, each time she pulls up with her elbows and her upper arms.
army crawls
has started getting on all fours and rocking but unable to get forward motion.(started one week ago)
Sunday, March 27, 2011
whats up in my life....very depressing and just blah
It's been a while since I've blogged. Lots been going on. Mostly due to Chloe. Our little girl is 16 months old. She weighs 15lbs and she is severly behind in every area of life, to give you an idea here is a bullet point list I made for our genetist appointment last Friday (more on that in a moment):
Labels:
Angelman Syndrome,
Chloe,
life
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5 comments:
{hug}
Jessica,
We love you and are praying.
Eric
My love,
God could not have placed Chloe in the arms of a more loving mother and we could not have asked for a more perfect little girl.
I look forward to walking this journey with you with the Holy Spirit within and you by my side we will endure and overcome to the glory of God.
We will grieve your dreams with you, and help you think of new dreams! Also, I think I can help you on the homefront with the cleaning thing. I'll call you.
ya, I really didn't think that anyone read my blog, I post this and low and behold I get like 80 hits in one day. I just want to say that I am overwhelmed at life right now, but I am blown away at the love people have shown for us. Thank you so much. Alice, you may just be in over your head but I thank you soooo much. The thought of you seeing our messy house makes me what to throw up but the thought of a clean and orderly house makes me want to jump for joy. I think I'm an emotional crazy person right now. Anywho. Thank you.
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