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Vicki

Good for you! your getting well is the key!

Hugs

Kelley

new to group

Hi group,

I am new to this group, so I don't realy know where or how to

start. I have an 18 year old daughter who has been diagnosed with

bpd. I feel like I am the one going crazy tho. I am having a hard

time figuring out what is behaviour and what is a symptom of the

disorder. I am also afraid and on edge most times- terrified to

answer the phone in case she's tried killing herself again. She is

away at university. I feel horrible, like it is my fault that she is

suffering like this. I guess i just need a place to vent, where

people will understand. Rita

Send questions & concerns to WTOParentsOfBPs-owner . " Stop

Walking on Eggshells, " a primer for non-BPs can be ordered via 1-888-35-SHELL

(). For the table of contents, see

http://www.BPDCentral.com<http://www.bpdcentral.com/>

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  • 4 years later...

Hi there,

I just wanted to introduce myself to the group. I came over after the chelation group shut down and have been too busy with the kids to spend much time with the group but the last couple days have really enjoyed reading the posts. I get a lot out of other peoples experience and thank-you all for sharing them!

I've got 3 boys. The oldest is typical and the younger 2 regressed into autism nine months apart and have mitochondrial disease type 1. Just as I was overcoming the shock of my middle sons regression and learning about what to do my baby (he's 3 today) started to regress. He was 15 months at the time.

My boys are on a modified SCD diet (with no casin, yeast, low phenol and sugar). We are also chelating, do namenda, valtrex, B-12, naltrexone, fluconazole and loads of supplements. My children are low functioning. My almost 5 year old started to put words together after we started valtrex but my little one didn't respond. Both boys autism is so similar as far as behavior and blood work the older one is having slow but gradual gains but my baby doesn't respond to much. He regressed in school last year so he has a home ABA program (40 hrs) a week from the school this year ( we gave him 20 hrs. last year after full day preschool) and hes picking up some sign but the biomed doesn't seem to do much for him so far. I know it works cause it is working on my other son. I'm switching DAN! Dr.'s next month hoping that Dr. Rossignal will help us with HBOT. My youngest almost died in the spring because of a reaction to clonidine and I'm pretty sure my current DAN! is now afraid to try things with him.

I'm active in trying to get insurance coverage for ABA therapy because I believe that once we clean these little guys up, with biomed., they respond best to the intense 1:1 intervention. I recognize some of the people on here from other lists and look forward to sharing hope with all of you. If your interested in seeing my little guys go to http://www.autismvotes.org/site/c.frKNI3PCImE/b.4445103/k.D5E8/Virginia.htm Autism Votes Virginia and click on the cute little guy, that would be my youngest Korlan or you can look at his webpage (it really needs to be updated) www.korlanneedsyourhelp.org .

Take care, Casandra

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