Showing posts with label Isaiah. Show all posts
Showing posts with label Isaiah. Show all posts

Friday, February 20, 2009

stupid

When I called the house tonight from work to say hi to the kids, Zae was really upset...I guess he got a note sent home, that this last time he was sick (w/ strep) put him at 5 missed days for the school year...the kids are only aloud 4 sick days a year...so now he has to stay after school twice next week. He said his feeling are hurt (I think he just means he's sad but doesn't know how to express that)...I feel so guilty though, one day he missed because I was soooo horribly sick I just couldn't get him ready and off to school, it was the one and only time I've used a sick day at work in a year. But as the mom I should have pushed harder and MADE myself get him ready, I feel so bad that he has to suffer because of me now. But honestly I think the 4 sick day rule is a little over the top, hell I get more than that for work and I'm adult!!!...I understand we're an exemplary school district and it's important for kids to be in school blah blah blah...but I am NOT sending my kids to school w/ strep! And the more they force parents to send their kids in sick the more the kids are going to GET sick @@@@@@@@@@.

Thank goodness last year they were aloud 10 missed days, last year Isaiah was phobic of thunderstorms...he has bad anxiety issues, as well as sensory issues...and thunderstorms were too much for him, if it was storming i couldn't get him to school he was in full meltdown mode. I mean it was fright or flight, pure terror...so he missed probably 5 days to being sick and probably 5 due to storms.

I don't know I'm just annoyed and feeling guilty...so thought I'd vent and tell on myself lol.

Sunday, December 21, 2008

Finding Isaiah's missing Pieces

I have to say I get quite excited whenever I find anything medically that pertains to Isaiah, it's like someone took a puzzle and shook it up and dropped the pieces all over the place and I am looking all over for them trying to put him back together. Every piece of imformation I find feels like another puzzle piece getting me that much closer to having my son back.

The first 5 years of Isaiah's life he was mildly autistic, for the most part we had our son, with glimpses of autism. We often forgot he was autistic, his biggest problem was that he couldn't communicate, (he talked but you couldn't hold a conversation with him) he was a little more hyper and had more meltdowns than the average 5 year old, but it wasn't horrible. Then in Kindergarten everything changed...if I knew then what I know now I would have NEVER have gotten his kindergarten shots! But I trusted my Dr. who has an article hanging in every room that vaccines do not cause autism. After that I lost my son, we rarely see the little boy we saw before. Before we had Isaiah w/ glimpses of autism, now we have autism w/ glimpses of Isaiah...it's like he's trapped in there.

That is when I began searching to find him again...so every little piece of the puzzle I feel like gets me that much closer to finding my son, and maybe getting him back. When we first moved to our house 2 years ago our neighbors would say wow I'd never guess he's autistic...it was only when you'd try to have a conversation with him...now they won't let their kids play with him because he's too "bad"...it's been a heartbreaking 2 years losing him like this.

Since we've started biomed I've started to see my son more often, God how I've missed him! I don't know how far we'll be able to recover our son. Every time I find a new piece to his puzzle its like a high...and it feels so good to finally have hope again!

Saturday, December 20, 2008

Cod Liver Oil Study

This is the newest med we are doing w/ Isaiah, his Dr. put him on Cod Liver Oil...as I did my part to make sure I am as educated as possible on Isaiah's treatments I found one medical paper by Dr Mary Megson in which she discusses in a scientific way her work around cod liver oil supplementation, principally in relation to Autism, it had so much information that pertained to me and Isaiah. This was a very interesting paper...I got lots of great information out of it, so I thought I'd share, and as I read it jotted down my thoughts and feelings along the way...

In the very first paragraph it discusses the link between autism and the pertussis vaccine, which I find ironic running across this in the wake of the DOD announcement that DTaP causes autism.

Just in the beginning she talks about one or more parents of these children suffering night blindness, that pertains in our case (me), she also mentions the thyroid...which Isaiah has a rare genetic condition, that my grandfather shares, (it's x linked recessive so I am a carrier and all my sons have it) where on paper he appears to have hyperthyroidism, although he does not. I just feel like we're finding more and more pieces to Isaiah's puzzle here!

I can't copy and past from the paper because of the form it's downloaded in, but I have a link below,

She talks about disorders of the eye, which when Isaiah was diagnosed with his eye muscles are weak and his eyes don't come together properly(which for the life of me I can't remember the name of right now, the eye Dr. said it was common in autistic children)...also the other thing that grabbed my attention was families with Colon Cancer, which we do have a family history of on my mothers side.

I highly recommend you taking a few minutes and reading this medical paper


http://www.scribd.com/doc/2574676/Cod-Liver-Oil-suplementation-for-autism-and-psychological-disorders

Sunday, November 23, 2008

The Progress We've Made!

Well, as of today it has been exactly one month since our very first appt w/ our DAN! Dr. I NEVER would have guessed that, in a months time I would have gone from skeptic to believer!!! Yes, when I very first heard about this whole biomed "movement" I thought it was just a bunch of parents who were seeing what they wanted to see while throwing all their $$$ out the window. So I say I went into this more than skeptical, I expected it to fail, The progress Isaiah has made in a months time is phenomenal. The biggest change in our/his lives to date is the meltdowns! A month ago Isaiah had on average close to 20 meltdowns a day...now we are down to maybe 1 or 2 a WEEK!!!!! Yes a WEEK!! I would have been FLOORED w/ one or 2 DAY, but a WEEK, this has CHANGED the quality of our LIVES DRAMATICALLY!!! Fixing all the problems in his body is going to take alot of time, there is still alot of work to be done, but the fact that THIS much has changed this fast gives me great hope for our future...for the first time ever.

Thursday, November 13, 2008

wow

OMG, so last night I was at work, and I called the kids on my lunch break and Isaiah informs me that he ate a piece of toast, apparently Rob made the kids cinnamon toast, Isaiah's on his bread, and Xanders on reg bread...Xander didn't finish his piece, and I guess Isaiah ate it...this kid is NUTS this morning!!! I can't believe how horrible he's stimming, and making wild noises, and the spontaneous mischievous actions. ..like I had him in the bath, I went to pack his lunch and come back and he's wetting the dog...The past 2 weeks have been so wonderful, and peaceful ...I just can't believe one piece (actually less cuz Xander ate some of it) can do this to these kids, and to think I was giving him 2 pieces everyday, along w/ other gluten and casein products. It's just amazing!

Wednesday, November 12, 2008

I'm still here.....

The first time I heard this song, it melted my heart, the words just seemed like they could be from an autistic child talking to the world. This is one of my new favorite songs, I put some of Isaiah's pictures and set them to the music...

Thursday, November 6, 2008

Afraid to jinx it

So I've been thinking it, but have been too scared to say it out loud, praying it isn't just a coincidence...but I think I can safely say I am seeing a change in Isaiah...he stims so much less now, he's not as hyper, his meltdowns aren't quite as frequent. Getting ready for school this week has been almost easy! He hasn't battled me about eating, he has had some mild meltdowns, and some stimming but not near as much as usual. Today Tierra and I went to walmart and I asked Tierra if Isaiah seems different to her at all, she said YES HE DOESN'T DO THIS (mimicked his usual hyper jumping up and down w/ making a weird noise stim). My heart just melted, ok it wasn't just me seeing what I want to see, someone else sees it too! And she's pretty impartial. I mean she knows we've found a new Dr. and are trying things to help Isaiah be more normal, but she doesn't know any of the details, or what might change. So I feel I can safely share this, I am almost certain, my baby is healing!!!

Here's what we've done so far...
October 23, Met our DAN, and began mixing the Biomed w/ chiropractics and acupuncture (not needles just a painless laser)
October 24, started the GF/CF barely soy diet,
October 30, started epson salt baths
October 31, 2nd appt w/ DAN, this is also the day we noticed his psoriasis that we've been battling for 4 years had magically disappeared
November 3, began taking Probiotics...

Sunday, November 2, 2008

What Isaiah wants everyone to know...

A friend of mine has this posted on her myspace, and it really hit home with me...I hope everyone who ever comes in contact with Isaiah, or any autistic kid for that matter, would read this, and get a small glimps into what life is like for our children.

Nobody can see my disability. I look just like every other kid -- attractive, walking, making sounds. They can't see how my neurons are scrambles in my brain. They can't see the misconnections between my left and right brain. Nobody can see that I have autism spectrum disorder. Nobody can see that my body is sick. No one can see that my stomach is in knots from my digestive system not working. No one can see that my body and mind are starving because my cells don't make the right enzymes to digest food. No one can see that I suffer from low blood sugar because i can't properly metabolize nourishment. No one can see that my body is attacking its own nerve cells from autoimmune dysfunction. No one can see that mercury ,lead, and arsenic cannot be excreted from my body, so it keeps building up in my brain. No one understands that my body cannot tolerate normal enjoyments for children, like bright, vivid colors and loud noises. I desperately want to be a kid and enjoy these things, but my body just won't let me. But everybody can see how inappropriate my behavior can be when I am out in public. Everybody can see how immature I can be compared to other kids my age. Everyone sees the 2-year-old's tantrum when things have been too overwhelming for me. Everyone sees my frustration from trying to cope. Everyone sees my screaming & fighting. Everyone just assumes I'm being bad, not that my body hurts, my eyes are in pain from colors, my ears ring with loud noises not heard by others. Everybody sees my tantrums when I don't get my way. No one sees that I can't explain my fear when I think I'm not being understood. Everyone may see me scream if my mom takes something away from me. No one can see that having something of comfort can keep my fears under control for me, and taking it away makes my nerves explode in anxiety. No one understands how hard I have to work just to keep my behavior from reacting to the chemical imbalances in my body that make me feel horrible. No one can see that, no matter how hard I try, sometimes I cannot control it. No one can see the shame I feel after I've had a meltdown from my body's problems. What they don't see is that I'm a person. I have feelings and want to be loved and accepted like everyone else. What they don't see is that, when they look at me like I need a good spanking, I understand that I'm not capable of controlling my body. What they don't see is that I scream because I don't know how to say, "Help me." What they don't see is that I hear every ugly word they say, but for the life of me, I can't make my mouth say what I'm feeling. But they don't see that as a disability. They say I'm unmanageable. They say I'm a problem .But I'm not a problem. I have autism spectrum disorder. My mom has taken me to more specialists than you can ever imagine. She's read more books and done more research on my disease than a parent would ever want. She has tried special diets, supplements, drugs, and various metabolic therapies. She has prayed for guidance and asked for discernment on how to help my body. And behavior, oh yes, has she tried everything to help my behavior. Stop telling her all I need is a spanking. If a spanking would stop all this, my mom would gladly exchange my disability for a spanking. She knows better than any of you what I need to help me, and what we both need is your understanding, not ignorance. I just want to be accepted and understood. No blamed and shamed. I want to be appreciated for my gifts. I do have some if you look more closely. I want to be cared for as a person. I want you to care, even when I act like I don't. I want to be respected, just like you do. I want you to respect my mom and dad for all the hard work they have done to help me try to lead as normal a life as possible. I want you to respect my family and all the struggles we have endured because of our love for each other. I want to be loved like any other child. And I need you to role model respectful behavior for me so I can be respectful, too. I want you to love me just like Jesus would. Debi Tyree

Friday, October 10, 2008

I wrote the teacher

So here was her responce, I just LOVE his teacher!

Mrs. ****,

I'm so sorry to hear that he is feeling left out. It appears that there is some apprehension or shyness when he's in the classroom with the students. When we work in small groups he seems to feel proud when he excels and interacts with the kids. However I feel it is very important to help him feel more comfortable with his classmates. I will check on places Isaiah isn't in my class to see if there are kids he's playing with at times. I will also find out who he would like to play or work with and buddy them up. Do you feel he would like to be moved to another table and sit with other kids? I can move several students if you think it will help.

The things we try will be done in such a way that he won't be singled out. Your input and suggestions are very important. Let me know what you think of the suggestions I have.

Wednesday, August 20, 2008

I can't believe this is happening!!!


Isaiah started first grade today. He's been so excited about it, I thought he would jump out of bed and drag me out of the house this morning. But instead he woke up and said "I can't believe this is happening" lol!!! My baby was NERVOUS!!! He knows he's in for a long day. He wouldn't even eat breakfast the poor thing! But he got dressed with the cute little outfit his sister picked out for him, and grabbed his over stuffed back pack and his lunch lovingly packed by his mama and trotted out the door. He was unusually quiet the whole ride to school. We got there, and I walked him in and he met his teacher and recognized a few of his friends (and of course the one kid he can't stand ended up in his class lol). I'm so nervous for him! I hope he does ok...man I wish I could be a fly on the wall in his class today!!!