Guest guest Posted December 29, 2007 Report Share Posted December 29, 2007 My boys have thankfully come a long way. That have taught us so much. Logan was just taken to get re-evaluated and they said it looked more like ADHD that ASD. : ) He still is very active and distractable and can go from 0 to 60 in the excitement category. He is still on many supplements, but we learned an important lesson about getting too comfortable with recovery. He is very fragile metabolically and we made some decisions that led to a recent regression. He has PANDAS and it was in remission. Logan was doing so well that we stopped the anti-strep herbs and the microbial RNA that had helped him so much. Well he came down with a horrible case of strep (no sore throat, but a scarlett fever rash) that completely changed his behavior, eye contact, sensory system etc. He even developed a very scary facial tick and made sounds under his breath like a train. I was so upset. He was the one I was done with! Well- regardless of what people tell would lead you to believe if your child is meatbolically fragile- you are never " done. " Never let your guard down- trust me! This all happened in mid October and now he is almost back to normal. He is just more hyper than usual. The facial tick is gone, sounds are under control, fine motor skills are almost back to normal and he is more sensory regulated. Most people would never know what he has been through recently or before. You used to ask him his name and he couldn't respond. He couldn't answer why, how or even what questions. Now he talks like any other 6 year old. Now he has lots of friends at school and plays on a t-ball team. He is happy which is all that I care about. He is learning to play golf with his daddy and is a very good reader. I often find him reading chapter books in his room. (Not bad for six.) 's improvement is the most dramatic, but he still has autism. He is 4. He is so with it now and follows directions spoken to him in a conversation out of the context of a routine. IE- He wanted to take a bath and my husband said. " We need to clean out the tub first. Let's get a cup " He ran to the kitchen by himself and dumped out a plastic cup's ice water and ran to give it to his daddy. He now is beginning to answer questions more readily and tells us what he wants. has apraxia and along with this he has articulation problems. C is pronounced T etc. He plays with other kids, but has a hard time if the play turns more language based. His eye contact is great. He gives these mischevious looks and raises his eye brows like " look what I'm gonna do. " He has quite the personality. VSL3 (probiotic)LDN, IVIG, and Deplin (Rx strength folic acid) have been very helpful recently. IV secretin also helped him to start gaining weight. I just recently posted about his rash that we call " his valtrex rash " that came out with IVIG. He never held a titer to the varicella vaccine. (MMR and varicella vaccines helped him to crash into autism quite dramatically.) used to bang his head, not acknowledge others in the room, cry when he wanted something with out gesturing, pointing etc. Stomach aches, up all night crying, no naps, no sleep. UGH! Now he sleeps all night, communicates effectively, runs up to me and says " Mommy. " He smiles and tries get my attention by doing things he is not supposed to do while grinning. He knows his letters and sounds and is reading sight words. He still has a far way to go in the language department, but we are feeling like he is " here with us now " where as before he was a million miles into his own world. Here is to hope! Recovery and improvement is possible! It just takes A LOT of reasearch , A LOT of hard work, A LOT of good therapies, A LOT of advocacy, an awesome DAN! doc, and unfortunately A LOT of $ invested. We drained our savings, our equity, our retirement and our credit cards- but I must say the " I love you mommy " got from last night made it worth every penny. I may have to teach kindergarten until I die- LOL! But at least I'll understand the kiddos on the spectrum in my class and my boys will have a future that no one thought that they would have. : ) Jeanine > > > > I posted earlier and can't find it to repost. My son is much worse > > with his OCD, lining up, etc. and has had fever blisters on and off > > since we started valtrex almost a month ago. Is this normal? Should > > I continue even though he seems to be regressing? > > > > Thanks, > > Crystal > > > > > > > > > --------------------------------- > Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2007 Report Share Posted December 29, 2007 > Thank you for posting this reply. It is always beneficial to gleam encouragement and pearls of wisdom from those who have gone before you on a recovery journey. I've found that older posts in the archives have proven to provide strength, inspriration and patience. > Yes, thank you all for replying. There were a few questions from earlier I wanted to answer. My son does eat yeasty foods, but is GFCFSF with about 40 other food allergies. We're taking Yeast Aid by Kirkman. Should we do something more potent? I've never been able to tell yeast meds help him, but he's never been on a yeast free diet as far as fruit and flour. He is very thin and will not eat. We've been doing DAN for over a year and I can't really tell too much of a difference. How long are you supposed to stay on Valtrex? Are there other things to do to go along with it? I did search the files and didn't find any. Thanks, Crystal Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2007 Report Share Posted December 29, 2007 You are too kind. My boys are both on GF/CF corn free and soy free diets. Logan also becomes anaphylactic to beef, eggs and peanuts. So, feeding time used to be tricky, but is no big deal any more. My husband and I eat GF/CF/ CF as well. It helps for the kids to see us eating the same foods and I feel sooo much better- no more tummy aches for mom either : )! Good luck to you on your son's journey. > > > > > > I posted earlier and can't find it to repost. My son is much worse > > > with his OCD, lining up, etc. and has had fever blisters on and off > > > since we started valtrex almost a month ago. Is this normal? Should > > > I continue even though he seems to be regressing? > > > > > > Thanks, > > > Crystal > > > > > > > > > > > > > > > > > --------------------------------- > > Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. > > > > > > > > > --------------------------------- > Never miss a thing. Make Yahoo your homepage. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2007 Report Share Posted December 29, 2007 Hi Crystal- My son was (is) a tough cookie too. It is so interesting how much the gut plays a role in all of this. We used glucosamine to decrease the inflammation in his gut and the very strong pro-biotic VSL 3 (available at Apothecary shops w/o an RX) Diflucan has helped as well. Your son's refusal of foods might be a sign that he is still having pain when eating. Maybe the VSL 3 would help. It is used for ulcerative colitis and Chrons disease. We found that removing corn was very helpful for . It can cause many allergies and pain. Have you tried digestive enzymes? Maybe your son is not fully digesting the foods he is eating and this is causing pain. We follow the resarch of Amy Yasko and found that the Bowel Support RNA immediately cleared up any stomach problem that was having. Also, when we adequately supported 's methyl donors he began to have normal colored poop. He takes Deplin, which is an RX for folic acid. So, many factors are at play with the gut. I hope this helps. Good luck and feel free to private e-mail me. I will be more than happy to share or help if I can. : ) Jeanine > > > > Thank you for posting this reply. It is always beneficial to gleam > encouragement and pearls of wisdom from those who have gone before you > on a recovery journey. I've found that older posts in the archives > have proven to provide strength, inspriration and patience. > > > > > Yes, thank you all for replying. There were a few questions from > earlier I wanted to answer. My son does eat yeasty foods, but is > GFCFSF with about 40 other food allergies. We're taking Yeast Aid by > Kirkman. Should we do something more potent? I've never been able to > tell yeast meds help him, but he's never been on a yeast free diet as > far as fruit and flour. He is very thin and will not eat. We've been > doing DAN for over a year and I can't really tell too much of a > difference. How long are you supposed to stay on Valtrex? Are there > other things to do to go along with it? I did search the files and > didn't find any. > > Thanks, > Crystal > Quote Link to comment Share on other sites More sharing options...
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