Showing posts with label muscle testing. Show all posts
Showing posts with label muscle testing. Show all posts

Thursday, July 24, 2014

East Meets West...

This morning started out how every morning this week has begun.  Each morning, while Hope takes a little nap, Brian and I attend Lego Therapy together in "his" (Gavin's) bedroom.  Oh, don't even laugh.  Lego Therapy is very serious.  *wink*  It's good for him - he uses his imagination and is learning how to build things.  It's good for me!  I get lost in the mindless connecting of lego bricks.  But it's best for us.  We never look at each other - only at our "masterpieces."  The activity and the lack of eye contact removes the vulnerability... and allows Brian to open up to me in ways he usually doesn't.
Yes, Lego Therapy is very serious.  And I'm honored that Brian invited me to join him.
After this morning's therapy, we got in the car to take Hope to the doctor.  While we were in Ocean City, a rash that was "here and there" and not worrying me much at all turned into a fully body rash that looked familiar.  It didn't look exactly like the contact dermatitis that I was used to seeing with Gavin over the years.  And it didn't look exactly like the eczema that I also saw with Gavin.  I had my suspicions... but I wanted the doctor to see her to rule out any illness or other reason for the rash.

First she got her weigh in...
She looks enormous here - but she's actually quite petite!
Hope's fightin' weight is now 16lbs, 12oz.  She will be 8 months in less than a week.
As soon as the pediatrician walked in and saw her rash, he said it was classic eczema.  I felt relieved that it wasn't an illness or anything very serious.  I left with a script for a steroid cream that I likely won't use.
Our next stop was to see Dr. Kang.  Because of her (and the other alternative doctors and nutritionist that I have on my "team") I know that everything begins internally.  When I was told it was Eczema and I should just moisturize and hope that she grows out of it down the road, I felt that it couldn't be entirely true.  Don't get me wrong - I have great respect for our pediatricians (they know that).  And I'm not trying to come across like I know more than they do (because I don't!).  I am really grateful that they have always been supportive of me - since Gavin was an infant! - as I tried all different types of alternative therapies and medicines and treatments... and then reported back to them with my results.  Some worked - some didn't - but none of them harmed my children along the way.  I need all of our doctors - traditional and non-traditional.  East meets West in our marriage... and in our healthcare team!
My suspicion going in to see Dr. Kang was that this was food related - and I strongly suspected Mango.  Hope didn't have any of these issues until I introduced food.  Then this morning I received an email from a reader who, coincidentally, uses the same type of doctor that does the same type of muscle testing that Dr. Kang uses.  She told me about her daughter who would get a rash every time they'd go to the beach (or throughout the summer) - and it turned out to be an allergy to sunscreen!  Bingo!  I hadn't thought of that!  So after reading her email, I quickly grabbed the sunscreen I used on Hope (Badger Sport Zinc based sunscreen) and headed out the door.
We got to Dr. Kang's and I told her about the new diagnosis... and my theories about the food and sunscreen.  With Hope sitting in her stroller, she tested me first.  I didn't show any reaction to the foods or the sunscreen.  Then she picked up Hope and put her down on the table next to me.  I held her hand with the vials representing the foods sandwiched between our skin.  Sure enough - she showed a reaction to fruit - evidenced by my weakness as Dr. Kang tried to push down my arm.  When she tested me without Hope, she couldn't push my arm down at all!  Next, Dr. Kang smeared some of the sunscreen onto my arm.  I held Hope's hand again and - she showed a reaction.  Can you believe this? You can't make this stuff up!!
Dr. Kang's advice was to follow the same back massage treatments on Hope that I have done (and still do) on Brian.  I will put mango in a glass baby food jar (and every other fruit I feed her - banana and avocado - just in case) - tuck the jar into her pant leg or waistband so it's touching her skin - and massage down both sides of her spine in a tapping motion.  This will balance her immune system and desensitize her to the "allergens."  I will also do this with the sunscreen.  "Why don't you just use a different sunscreen??"  I hear you asking.  Because I feel like I found a quality sunscreen that is safe and better for their skin than many others out there.  I'd rather make this one work for her than try a list of other ones that might cause a reaction - maybe even a worse one!  
She also suggested that before I introduce a new food, I should do the glass jar technique for two days prior.  This should eliminate any problems with the new foods!  And, she truly felt this would eliminate the eczema issues.  Since I was able to eliminate Brian's peanut allergy using her techniques, I tend to believe her.  Also, if you remember, I posted about Brian's skin issues several weeks ago.  Dr. Kang picked up a detergent allergy (which I eliminated) and an immune deficiency which showed up as skin rashes.  I diligently did back massages and he had two acupuncture treatments... and he's as good as new.  His skin looks great!
This does not mean I don't believe our doctors or don't respect their advice.  This just means that I'm open to the possibility that there could be another solution... a different way.  Knowing that it can't hurt Hope to try, I am going to be diligent with working to eliminate this issue.  I only wish that I had known Dr. Kang - or known this way of approaching illnesses and diagnoses - when Gavin was a baby.  He suffered terribly from eczema and contact dermatitis and reflux and allergies.  Knowing what I know now - and having the support I have now - I am sure we could have helped him so much more.  But when you know more... you do more.  And I know that he is smiling and proud in Heaven as I "do more" for his baby sister.
This will be a journey - and I feel confident that the outcome will be successful, but I could be wrong!  I'm taking you all along with me so we can experience this and learn together.  I'll be documenting the journey with photos of her rashes and we'll hopefully see them all disappear.  Here are some photos from today... 
 You may have noticed in some of the photos that Hope looks like she's crawling.  She is!!  It's very new that she's crawling on all fours.  I took this video today and it captures all the great things she's been doing lately:  crawling on all fours... motor planning as she figures out how to get to and then pick up what she wants... going from laying down to sitting up... army crawling (or doing the worm depending on how you look at it or what music is playing in the background at the time)... and problem solving!!  Check it out...

And finally - Brian's "Swim Fast" lessons.  He is doing great and having a lot of fun!  Today is day four and he was able to float on his back and flap his arms and legs to keep his face out of the water (for the most part).  His instructor (named Katie!) touched the back of his head here and there- but he mostly did this on his own!  I was really impressed!  (And Brian was extremely proud.)


Monday, February 25, 2013

Fascinating Discovery...

I mentioned in yesterday's post that I had contacted a "Medical Intuitive" named Anthony Williams. Basically, he's  a psychic who can tell you what's wrong with you. We wanted to see if he had any insight into what might be going on with Gavin. I'll admit that Ed and I are open to these types of things.  Sure, there are some quacks out there - "Boardwalk Psychics" and people who take your money - but there are also people who really have a special gift.  Not knowing which one we'd encounter yesterday - we really took a chance.  A $350 an hour chance.  We figured we had nothing to lose...except $350.


(Please read this post for an update in 2016 BEFORE contacting him!!)

Anthony Williams told me that he believed Mercury was Gavin's issue.  And mine, too.  That I passed on a mercury sensitivity - along with actual mercury - to him in utero.  That it caused neurological damage and even explained his features, or birth defects.  He told me his suggestions for supplements that I could give Gavin to help eliminate the Mercury slowly and safely from his system and he really thought we'd see great improvement from Gavin rather quickly.

I wasn't a total disbeliever yesterday.  But I wasn't sure I was totally "sold" on the idea.  I would definitely say I was intrigued.  The way I saw it, giving Gavin supplements and making small changes in his diet couldn't hurt him.  And I knew my next step would be to consult Dr. Kang, our acupuncturist immediately.  She has successfully tested the boys for allergies before and has not only been 100% accurate with her non-invasive muscle testing... but she helped me to ELIMINATE Brian's peanut allergy.  (Much to the shock of his traditional allergist)

After school today, Gavin and I headed to see Dr. Kang.  I explained the entire situation to her.  The blog competition - the influx of traffic - the tons of suggestions and referrals - the "medical medium" - and the mercury theory.  She seemed a little bit skeptical of the medium, but agreed to test both Gavin and me for mercury.  Sure enough - Gavin and I both tested for mercury.  First she had me hold a vial representing mercury in one hand while I held my opposite arm straight out in the air.  She pushed down on my arm with all her strength and asked me to try to keep my arm in the air.  I could barely keep my arm up.  Then, still holding the vial, I had to hold Gavin's hand.  She would test him using me as a surrogate.  This time, I had ZERO strength when she pushed down on my arm.  Looks like Gavin has it worse than I do - the mercury has to go.  Dr. Kang told me to get both of our blood drawn to test the mercury levels, so I'm looking into the best ways to do that.

Is this it?  Could this be the "diagnosis" I've been searching for?  I really don't know.  Ed and I are both on board with working to remove the mercury from my body AND Gavin's and see what happens - knowing it can't hurt.  In the meantime, however, I will still pursue other avenues and genetic testing.  It's very possible that Gavin has a mercury issue and a genetic disorder on top of it.

I've already started Gavin on the supplements today!  Anthony recommended that he take the following:

Liquid B12 - He told me that Gavin uses up more B12 in his nervous system because he has to work much harder than we do.

Liquid Zinc - This will support his endocrine system and boost immunity.

Hawaiin Spirulina Powder - This is to support his brain and nervous system.

Liquid Ginkgo Leaf - Not as a "memory booster"... but to support his neurological system.

Melatonin.  We have been giving him Melatonin routinely at night for the last two or so years and had no idea it had other benefits besides to help him fall asleep!  Gavin really needed assistance - otherwise, he'd be up every night playing in his bed until midnight!  Anthony said that Melatonin acts like an anti inflammatory agent in the brain.  It also helps repair nerve damage and electrical impulse issues.  I feel good that we might have been "helping" him without even knowing it!  Gavin also had a head start with nutrition thanks to Dr. Coralee Thompson.  I consulted with her when Gavin was a baby and she designed an entire nutrition and health program that he follows to this day.  She ended up writing a fabulous book that I highly recommend - "Healthy Brains, Healthy Children" - whether your child has issues or not!

As for his diet, Anthony simply suggested decreasing the fat somewhat and increasing sugar.  He told me that Gavin needs ten times the amount of sugar (natural sugar - not candy or juice) than 'normal.'  He expends more energy to do things and overworking his electrical impulses.  We generally add butter to every pureed meal he has - so we will just substitute that with applesauce.  He also told us to increase his fruit intake in general and to add cilantro to his veggie stew.

I've added "Zeolite" to my regimen.  I took the first dose this morning and - holy cow.  Let's just say it has already started to work.  Trust me.  You don't want to know the gory details.

These are all very easy things!  I'm really excited to see how Gavin progresses over the next few months.  I hope you are, too!

Over the weekend, Gavin shocked us by deciding to walk more than he ever has.  He was even turning himself around on his own to walk in a different direction!  I was too busy hovering over him to grab a video, so Miss Sara took one for me today.  Check out these two videos...and prepare to be amazed.

If Gavin is making this much progress now... can you even imagine what's ahead a few months from now?  I can't wait!

In other news... Brian has been kicked out of school!!
He has been attending a pre-school for help with his speech delay since January of last year.  He really loves it there - and we love his teachers, his speech therapist and his little friends.  But he really hasn't "needed" the extra help for quite some time, so the news didn't come as a shock to me.  I'm so grateful to his teacher, Miss Laura, and his speech therapist, Miss Maggie, for how hard they worked with and cared for him.  I'm currently "pre-school" shopping if anyone in the area has any suggestions or referrals!

I have a feeling before you know it Brian will be reading to Gavin... and Gavin will be complaining that he wanted a different book... and soon I'll be telling the boys to stop fighting with each other and to "keep it down"... and all my dreams will have come true in a big happy ending with a bow on top.

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