Showing posts with label medical intuitive. Show all posts
Showing posts with label medical intuitive. Show all posts

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.

Sunday, February 24, 2013

Thank You...

Today is the last day to vote in the Parents Magazine Blog Competition...up until midnight tonight... and I have to say, I'm relieved.  I am tired.  I am grateful.  I am glad that it is over.  And I am proud that I accomplished what I set out to do - bring as many eyes and smart minds and tender hearts here to try to help Gavin.

My writing has always been about Gavin.  To be honest, I often feel that my life's purpose has always been about Gavin.  I was sent here - and he was sent to me - so we could heal each other.  And we will. And maybe in the process we will help heal others, too.  
There's something about this little boy with the sweet smile and the fierce determination that has captured more than just his family's hearts.  I feel honored to share Gavin with the world.  And I truly mean the world.  Here are some of the countries you all visit us from...

Having all of you here means more than just a rising visit counter and collecting flags.  It means I learn from other parents who have travelled this road... I learn from medical professionals with advice to share... and, most importantly, I am reminded that I'm not alone.  Having a special needs child can be quite isolating.  You all have been the greatest company - whether you've been here over the last five years or just the last five days.  

The added exposure here has gifted me with new friends, wonderful suggestions, interesting referrals and a list of different syndromes and disorders to present to Gavin's medical team.  One of the referrals was to a medical intuitive, Anthony Williams.  I just finished an hour consultation with him and it was fascinating.  (Please read THIS UPDATE before you consider contacting Anthony Williams!!! A LOT has changed since I wrote this post) He is sure that I have high levels of mercury in my body - and that I am highly sensitive to mercury, which is causing my medical issues.  He also said that the majority of my miscarriages (I've lost 9 babies to date to miscarriage) were due to mercury toxicity. (Darcy's death - my 10th loss - was a true cord accident) This makes sense to me.  In my twenties I was very sick and no one knew what was wrong with me.  I was so weak that at one point I had a short stint in a wheelchair.  Luckily, we have a family dentist who has a holistic approach and he insisted that my mercury fillings needed to come out.  Out they came - and sure enough I quickly got better.  Anthony Williams thinks that Gavin has the same sensitivity as I do - and suffered from mercury poisoning in utero.  He told me that it can cause birth defects and neurological issues and it's not something that would show up in chromosome testing and we never thought to test it through blood work before.  There are supplements I can start adding to Gavin's diet (and mine) to start pulling the mercury out of his system - and won't harm him in any way in the process.  He sees Gavin making tremendous progress... walking and talking and eating... and living a long life.  The way I see it, working on removing mercury from our systems is something we can easily do while we continue our conventional quest as well.  It can't hurt!  I will be calling Dr. Kang, our wonderful acupuncturist, tomorrow.  I bet she'll be able to muscle test Gavin and me for mercury - and maybe she can help us with balancing our bodies and removing it at the same time!
I am so grateful for all the love and support that has come my way because of (and before) this competition.  And I'm grateful to those who voted - some every single day!  I know how busy life is so thinking of you taking the time to click into a site and vote for this blog - it's humbling.  Thank you.

And I want to thank the editors of Parents Magazine.  Thank you for choosing me... the girl who uses "..." and exclamation points entirely too much.  The girl who pours out her soul and overshares on a regular basis.  The girl who used your competition to expose her son's medical mystery to the world without having him sign a HIPPA form.  The girl who tweeted Snooki to "Vote for Chasing Rainbows."  (I'm sad to report she never tweeted me back.)

I am grateful for the validation that you gave me along with the nomination.  Validation that I should keep on doing what I'm doing.  That I should keep on working hard to help my children be the best that they can be using any means possible.  Readers may reach for tissues when they come to this site... 
...but you should all know that the Leong family is reaching for the stars.
Parents Blog Award Finalist 

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