Showing posts with label anthony williams. Show all posts
Showing posts with label anthony williams. Show all posts

Wednesday, February 17, 2016

The Things We Do When We're Desperate...

Have you ever been in a situation that made you feel so desperate that you were willing to try anything to make it better?

I have. It was called being Gavin's Mom.

I was constantly on a quest to make his life better in every way. Simple things like finding ways to make sure he felt included and could participate in family activities. Or figuring out ways to physically improve his life with equipment or clothing or shoes or aids or new therapies. I was always on a quest to improve his health and nutrition - and to keep his playroom neat and constantly interesting so he could move around and enjoy himself. But honestly, my greatest mission in life was to figure out his diagnosis - and that was the source of my desperation and most of my sleepless nights.

Back in February of 2013 - just a couple months before we would lose Gavin so suddenly - Chasing Rainbows was nominated for an award by Parent's Magazine. I never in a million years thought I would win - and didn't care. It was a huge honor to be noticed and nominated - but to be honest, it was MOST exciting to suddenly have a platform. I used it, shamelessly, to put Gavin into the universe - hoping that someone out there would recognize something in him that would lead to a diagnosis. 

It was a fascinating experience. I got a lot of suggestions... a lot of "Gavin looks like my child who has"... ideas for tests to ask for... and a reader who suggested that I contact a "Medical Medium" by the name of Anthony Williams. I took every suggestion and every thought seriously. I sent an email to Gavin's geneticist that same day and asked her what she thought of a list of new syndromes and disorders. And I immediately contacted Anthony Williams and got an appointment almost overnight. The call at that time was $350 for an hour. (It is now $500 for a HALF hour) I remember sitting on the phone waiting to talk to Anthony and I was so, so excited. I was sure I was about to get the answers about Gavin that I had been searching for since the day he was born.

I explained to him my desperation to get answers about Gavin's mysterious, undiagnosed genetic syndrome. He spent the first ten minutes or so talking about supplements. The history, which brands he prefers, which supplements help with what. Then he told me that mercury was the cause of Gavin's issues - that I passed actual mercury on to him and a mercury sensitivity in utero, causing his physical, neurological and developmental issues and explaining his features. Basically, that he suffered mercury poisoning in my womb. He said that was the cause of all of my miscarriages as well (nine at that time). He also said I had the Epstein-Barr Virus in my system. Then... it was back to supplements again. He was a very nice person so I tried to remain patient. I thought he was just getting off track and would get back to helping me with our medical mystery. 

He didn't.

I watched the clock tick and tock - and watched our money continue to fly out the window - as he spent 95% of our call discussing supplements and telling me to write down which brands of supplements to give Gavin and which I should take. I wondered, in frustration, if he got a kickback from supplement companies! You can read that original post here.

I hung up feeling very upset... very foolish... and extremely dissatisfied. I had been told he could "diagnose" and I didn't get that. But - if you know what it feels like to be desperate, then you know what I did next. I convinced myself that maybe that was exactly what I needed to hear. Maybe the supplements WERE the answer! Maybe Gavin's issues WERE "my fault" when I passed on mercury to him. So I went out and bought all the expensive supplements and made small dietary changes. I did them all for Gavin and for me.

Just forty eight days after that call, Gavin died of a random febrile seizure that stopped his heart and led to brain death. He was gone - only 5 1/2 years old.

For months, I stressed and questioned doctor after doctor about the supplements wondering if we hurt him in any way or they led to his death. It was an excruciating time. (Thankfully, every doctor assured us it was not our fault and the supplements were not at all the cause.)

After Gavin died, Anthony William's assistant called and said he requested that we call him. I suppose he either read that Gavin died on my blog or saw it on social media. I did NOT appreciate being summoned by him when it was my son that died, after all. I never called him - and he never called again.

Since that time, I have received close to 500 emails from people who googled Anthony Williams, found my post and have questions. Most of them are writing to ask my opinion before they put themselves on a waiting list for a $500 call. Many have written to tell me about their call - and how they won his "lottery" and were picked for an appointment. I answer every email personally - even though 75% of them end with "I hope Gavin is doing well!" I suppose it has been my new mission to keep people from making the same, foolish mistake that I did.

The following comments are all "alleged" experiences by those who have had appointments with the medical medium, have bought his new book or have listened to his radio show. I want to emphasize the word "ALLEGED" so no one comes after me.  ;-)

Over the last month or so I could tell that something had shifted because I started to receive at least ten emails each day. It turns out that Anthony Williams released a book. I was told by many people that they were offered incentives to give his book five star ratings on Amazon - prizes, autographs, etc. I personally feel like that is immoral... especially toward desperate individuals who are seeking answers and then are misled by all the praise! At one point he was offering a $3,000 prize for the most inspiring Amazon review. I'm sure the "winner" was someone from his publishing team. You'll be hard pressed to find anything negative about him anywhere on the internet (which is one of the reasons why I'm writing this post). I am quite sure he has a team of people keeping his image squeaky clean. You'll notice his Facebook page doesn't allow visitor posts - and he personally answers every single comment under his own posts. I'm not sure if he's a "medium" or a "nutritionist" - nearly every post is about what supplement to take and not focused on medical issues. People who are gravely ill contact him which makes me very sad.

ALLEGEDLY, the "lottery pool" is a ploy to make every person feel "hand picked" and oh, so lucky. Everyone wins the "lottery" - and the prize is losing $500!

There seems to be a theme from people who have contacted him. He has (allegedly!) told them all that they (or their children) have the Epstein-Barr virus, shingles or mercury in their bodies - or have had mono as a kid. All of these things can explain anyone's symptoms. Then he puts everyone on a benign supplement regimen that is pretty standard and well known to anyone in the health care world. There is nothing "spirit-led" about it.

He claims that he is the only person in the world with this gift - as a medical intuitive. My personal opinion, but if Anthony Williams was the real deal, don't you think the internet would be blowing up with "I'm healed!" or even "I'm so much better because of his advice" stories? You don't see the internet blowing up because everyone is either ashamed that they fell for him, no longer with us or have just moved on with their life (less a big chunk of money). Allegedly, of course.

I feel glad when the people who don't have $500 to lose write to me and I can keep them from handing over their rent money... grocery money... and their hopes to him.

I feel sad when people write to me who are so, so sick or were like me and have a child they are desperate to help. I know their pain and their struggle and hate bursting their bubble with my story about my experience - and the many, many emails I've received from people who had the same experiences.

If you're thinking, "She's just bitter because her son died and wants someone to take it out on" - well, you're wrong. I tried it all for Gavin - including contacting a "medical medium." Or should I say, "THE" medical medium... since he claims he's the only person alive who has this special gift. Too bad The Medical Medium couldn't have given me a head's up that Gavin would have an issue that could cause his death. Perhaps there could have been a way we could have intervened.

Of course we couldn't have intervened - and of course he wouldn't have known that Gavin would die - because he's a fraud. 

Allegedly.

I know what it feels like to be desperate. I do. And I know what it feels like to be sick and want to be well. I feel that every day. But Anthony Williams is not your answer. 

I've answered hundreds and hundreds of emails since 2013, but hopefully this post will put an end to them. And hopefully Gavin and I will continue to help people by sharing our experience.

If you found this blog post by googling the Medical Medium, please consider this YOUR sign from above... save your money and your time and your pride. Do not contact him.

Some lessons are learned in hindsight, unfortunately.

(Boy, Gavin, our journey together continues to be a wild, interesting, twisty-turny, lesson-filled, sometimes bizarre (allegedly)... and always a loving one. I miss you so much.)

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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