HANDLE, Cranio, Enhansa

If anyone asked me what my three biggest "wow"s would be with Michael, these would have to be them. We have done so many things with him that have been miraculous (Tomatis, diet, etc.), but these are current and making a huge impact on him now.

We had Michael's HANDLE followup this afternoon. It is so remarkable for me to think back where he was last year when we started, and compare that child to the Michael we have now. Today he was interacting, asking questions, being polite, so many wonderful things. Last year he was shy, acting out, impatient. He still has a long way to go, but I am just so thrilled with his progress.

I think the biggest things he has gained from HANDLE have to be better vision, self-confidence and body awareness. He has always struggled with getting his eyes to work together, making distance reading and close work like writing extremely difficult for him. Now, when his schoolwork comes home I can actually read it! And, no more throwing pencils to get out of writing! Also, he really seems to have a much better idea of where his body is in space, letting him freely jump, run, and just be kid. I love it!

I think the CST works so well with HANDLE. As his therapist has been working on his frontal lobe and the two hemispheres of his brain working together, we are seeing huge gains in self control, expression, curiosity, and pretend play. I'm not 100% sure what to attribute to HANDLE and what to CST, but together, they make a whole new kid.

Underlying all these gains has to be the enhansa. Now that Michael is free of the chronic candida infection, his tummy problems are gone and so is his OCD and most of his aggression. I can see every day that as his body heals, his brain does too. It is hard to understand how yeast can do so much damage, but boy do I believe it! Plus, the anti-oxidants have to really help in reducing inflammation and just making him healthier.

So, after much introspection on the way home, I have to rave about my favorite three 'wow's -- at least for today!

It's never, ever too late!

It's been a rough week here because Steve has been out of town for the last several days. Michael and I have really missed him. So, when I saw a topic of 'hopeism' on Age of Autism, I knew I had to read it right away. I was smiling and crying at the same time, and counting all our blessings.

Sometimes I get so caught up in all the things that Michael can't do, I forget about all the wonderful things he CAN do, and does. Every day we get to see more of his personality, and it's awesome to see another parent getting to see parts of her daughter she thought she'd lost so many years ago.

So, go read, watch the video, and have a tissue ready!

What I find most ironic is the article above it, about Enhansa. I truly believe Michael has made such fantastic leaps this year because of Enhansa. So, having these two articles back to back is just perfect!

I'm In Love with Enhansa!

I never thought I’d be in love with a bright orange capsule – but I am, and it’s the real thing! We have had Michael on Enhansa for well over a month now, and have seen incredible results. But, let me start with a little background information.

Michael has been battling systemic yeast his whole life. We’ve tried Yeast Aid, Diflucan, Ketokenazole, you name it. Each would help for a little while, and then the yeast would come back in force. I had researched the anti-candida diets, but just couldn’t do it. Michael is so skinny to start with; I just couldn’t take away any more carbs.

This calendar year we started off with the Diflucan and then switched to the Ketokenazole. Toward the end of the second prescription, the yeast was under control but I was terrified of what would happen when we stopped taking the medicine. Plus, I was afraid of what damage taking such strong antifungals could cause long term.

I had heard really good things about Enhansa, and was perfectly primed to try it. So, when we started, the yeast was mostly under control, but still there. We started Michael with one 75mg capsule in the morning for a week. We added one capsule a week until we are now at 2 in the morning and 2 at night, for a total dose of 600mg a day.

It’s like we have a whole new child. He was doing great when we started, but his social interaction is really taking off, and his OCD is much better. Right now he and Steve are playing Mario Kart on the wii. They are talking back and forth about the game, strategies for doing better, and unlocking levels. It’s so nice to hear a back and forth conversation that is related to what they are doing together! Add in that he’s sharing and taking turns, and I’m completely over the moon.

Spring is staring and Michael has been asking to go to the park. Last year, he would go on a lot of the equipment, but shied away from a lot of the more challenging tasks. This year, he is doing absolutely everything. He’s still a little intimidated by walking over a mesh bridge that is at least 20 feet off the ground, but he does it. He’s still a little more cautious that most of the other kids, but he’s catching up fast. It’s so wonderful to see.

Even better, he’s starting to interact with some of the younger kids. He generally feels comfortable with children about 2 years younger than him – they tend to be quieter and move a little slower. He’s played on the teeter-totter a few times, and shared some of the equipment that requires sharing. It’s so awesome to watch.

The very best result by far though is that Michael is a much happier child. He smiles more, and laughs a genuine laugh. I was so used to the hyper yeast laugh (other parents of yeasty kids know what I’m talking about) that it was a surprise to hear a genuine, happy laugh. I think he’s feeling better overall, and is less bothered by what’s left of the OCD.

I’m tempted to bump him up one more capsule to 750mg a day, but we haven’t decided yet. For now, we’re holding steady at 600 and seeing a happy, connected child. What more could I ask ?

I do have one footnote to add. Through all of this we’ve been seeing an absolute angel of a CranioSacral therapist. She has worked wonders with Michael both before and during our Enhansa experience. So, I can’t say for sure what is due entirely to the Enhansa, and what to the CranioSacral. I tend the think the two work synergistically, so it’s not a very big footnote.

OK, I will

I'm sitting here shocked. Michael and I have both been sick for the last few days. He's on the mend, I'm not doing as well. Steve was upstairs checking on some things that he needs to do before going to a meeting tonight when his dinner 'dinged'.

I asked Michael (who is feeling well enough to be sent on errands) to go upstairs and tell him his dinner is ready. Immediate answer "OK, I will" and off he went. He delivered the exact message I asked.

I've never seen such cooperation as we have the last few days. Could it be the fever? Is it that he's on his second week of enhansa? We haven't had any side effects from the enhansa (unless they've been covered up by the cold), but wow. I'm speechless, and it's not just my lack of a voice!