Posts

Summa Summa Time - and someone's improving!

Image
We've moved out to our beloved Montauk for the Summer and someone loves the ocean air. We decided to take a break from Josie's typical schedule of back-to-back therapists and appointments all day. We all needed a break and I think Josie can use some new sensory experiences. That said, I did find an amazing OT in Montauk who is coming twice a week, so she's still getting some very good therapy. I really love this OT, Lori. The truth is that since we've been out here, I've had some scares that she was not progressing, but in the past few days, she's wow'd me. Today I almost cried when she basically rolled over by herself! She's moving so much more, scooting her little legs under her belly, and reaching for what she sees in front of her - with both hands! This is new. I recently described Josie's development like Groundhog Day, she's been developmentally 4 months since being 4 months - so for 15 months. I am pretty certain she's gaine

Heavy Feet! 18 Month Update

Image
Josie is now 18 months old. Here's an update... First, the most exciting news: At the last weigh-in with Dr. Wilkens (pediatrician), we finally saw the curve on the growth charts move up! Josie gained one pound and her head circumference increased by one centimeter! One lb./cm might not sound like a lot, but this hasn't happened in nearly 9 months! I would stand by that scale like a contestant on The Wheel of Fortune afraid of landing on Lose a Turn. Month after month, I'd wait for the digital number to hold steady and when it finally does, it always read between 16.8 - 17.5. How was this possible? Pat Sajak shakes his head like, sorry dude. Well, she is now 18.7 pounds, 30 inches tall, and her head is 43cm. That is still below the charts for weight and head, but seeing the line on the chart move diagonally upward and not horizontal is all that matters - we're in the game - on our way to solving the puzzle. For height, she is actually on the charts - about 8%. Su

Ready to Start.. The New Regimen

Image
We got the results from Wanda, the Naturopath I mentioned two posts ago. Just to refresh, Wanda did a saliva DNA test to find out what's going on inside that little body. She found....drumroll please... diphtheria and graphites and a deficiency of iron and nitrogen. Let's start with Diphtheria. The DTaP vaccine that babies get at 2 months, 4 months, and 6 months stands for: D - Diphtheria, T - Tetanus, and P - Pertussis. To be clear, Josie doesn't have the actual illness, but a significant amount of the Diphtheria toxin was found in her body. I'm just wondering how a baby gets the very bacteria that she was vaccinated three times to prevent? I'm trying to wrap my brain around this one. I'm doing research on the disease and the controversy around this specific vaccine. I won't bring my findings here as my focus and energy now is just to rid Josie of the toxin. And that's Phase One of Wanda's regimen. Wanda also found graphites aka lead. I asked wh

I See You... in Pittsburg

Image
We took another road trip this week - to Steelers Country. As if I care about football. I don't, but that's a shout out to Uncle Peter. So we went to see Dr. Christine Roman-Lantzy, who is one of the few experts in Cortical Vision Impairment (CVI). She actually wrote the book . I made this appointment in September so needless to say, I was very excited to finally meet her. Josie was diagnosed with CVI at around 9 months. It's actually amazing to me that the first opthamalogist we went to did tell me it's her brain and not her "vision" (the structure of her eyes are fine), but she never told me about CVI. The second opthamologist handed me a one-pager with the definition of CVI, but never discussed the importance of tackling it immediately with CVI-specific vision therapy. The next two eye doctors had nothing CVI-specific to tell me either. The fact is that a child with CVI has a great chance of overcoming most of the challenges if they engage in the corre

So much to say.. So much to say

Image
Dave Matthews popped in my head just as I was ready to write a title. I do have so much to say and I'm hoping I can keep this post organized. So just as I've been feeling that I need to head down a new road, I spoke with 4 different women and one man who gave me just that - a new hopeful direction. I finally spoke with other moms who have experienced a situation similar to ours and who can say their children are recovering. To hear those words - and I'll end the sentence there. While I was at intense PT with Josie, a woman named Melissa came in with her son Matthew. I've seen them there for months and I couldn't get over how great Matthew looked. He's younger than Josie and was walking like a champ. I told her Matthew seems absolutely fine and she says she credits her team for getting him caught up. Part of her team is a woman named Jodie Collins, a PT who does CranioSacral Therapy. Melissa actually gave me Jodie's card a while ago, but I thought I had b

Go to the ends of the Earth for you..

Image
We just got back from a Johnson family trip to the wild wild west - New Mexico - to see a Chinese Dr. named Dr. Jason Hao. Dr. Hao is one of the only Chinese doctors in the United States who practices an acupuncture method called Scalp Acupuncture. We did a lot of research on it and read many stories of people with severe brain injuries who, after just a few treatments, recovered. Paralyzed people started walking. When we spoke to Dr. Hao on the phone he was very confident he could help Josie. When asked what percent of his patients respond, he said "I'd like to say 100%, but most people don't believe that, so I'll say 99%." Music to my ears. He explained that it sounds like the neurotransmitters in Josie's brains aren't connecting and with Scalp Acupuncture he can get them to ignite. We decided to make it a family vacation and make it as exciting as possible for Tanner. I told him it's the start of our mission to visit all 50 United States. We d

We are the People

Image
This post is dedicated to the people who work with Josie day in and day out to help her grow stronger - aka Team Josie. We had our 6 month IFSP (Individualized Family Service Plan) meeting with Early Intervention recently to assess how Josie is coming along with her current services. I was told that EI is unlikely to increase her services as they are going through budget cuts, but that wasn't the case for Josie. The coordinators understood that Josie needs more. While she is showing some moderate improvements, she has not reached a single milestone yet. She's still not sitting up unassisted, rolling over, making consonant sounds and/or anything above those skills. I personally think she's got these skills in her repertoire, but she loves the attention from all these amazing women every day. Smart cookie. So all of her services were increased by one. She will now have Physical Therapy, Occupational Therapy, Speech Therapy and a Special Educator 3x week for 45 mins. And h