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Joined: Apr 2008
Posts: 3
Freshman Member
Hi My name is JoAnna, I was diagnosed with Mercury in 2006, Months after having my first son in 2005 (yes he is a miracle!) after many years of developing pretty much every symptom Andrew Cutler had in his book! I was born with Lupus so everyone just kinda contributed all my health issues to that. I had to live in a bubble, wear and use all ORGANIC, I was starving to death and down to eating Organic Turkey Broth! Mercury affects my breathing allot so its so hard to breath!
Come to find out I have genetic mercury posianing, meaning I got it when I was in the womb, passed down to me by my parents. I had to spend over a year on "Natural Cellular Defense" and getting my thyroid and digestion (as well as that can be put together ) Hormones, Vitamin D levels and so forth. Then in 2008 I was able to finnaly start DMSA, I started a month and a 1/2 and then I found out I was pregnant again!!! So then I had to stop and wow what a journey that was for the both of us, Aviosuly Im making this a very condensed story! I had my precious Jack Ryan On December 22nd 2008! I am finnaly offically starting the dmsa THIS SUNDAY, I am exited to get back to things again and GET WELL. Life is very challenging with Mercury plus on top of it I have to take care of my two children , one Sean may have Mercury posinaning frown We are waiting on more results, he has a allery to gluten , but I know it is easier to Chelate younger children he is 3 1/2 and babies than it is adults so if we have to do that at least we know what to do which is a blessing in itself!

I could not be making it through this without God's Strength he give me each and everyday! I have an awsome Husband who has supported me when manny others have not (family included), I love him so much. And I have two wonderful boys! So take hope all out there we can get through this , what a blessing we have the tools!!!! NOW HAVE THE ENDURANCE!

Joined: Dec 1999
Posts: 30,867
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Welcome to the forum.

I have spoken with many people who believe that they either got mercury poisoning from their parents or passed mercury poisoning down to their children.

I would be interested in knowing how they diagnosed you, that is, what test did they perform to determine that you had genetic mercury poisoning?

Thanks!


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Rashid Buttar has huge amounts of knowledge on this stuff. The guy is just awesome imo. One thing he mentions is the genetic predisposition for the inability to excrete mercury.(his cool sounding words not mine ). He has weekly free audio downloads,just gotta subscribe-

This is a Q and A with him and he mentions some genetics in it http://www.drbuttar.com/autismcall/

Joined: May 2008
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L
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Hi JoAnna, ((( Smiles )))

That is so interesting Samh that you brought up Rashis Buttar..
I was just reading his site yesterday on the subject of Dr. Rashid Buttar Speaks on the Dangers of DMSA.
http://www.drbuttar.com/blog/2008/08/dr-rashid-buttar-speaks-on-the-dangers-of-dmsa/

I was reading on the board last night about an FDA ban on it?
DMSA and my childrens doctors office said they haven't heard of any ban as they use DMSA.
They wanted me to send them what I had read on it.
But my children who are autistic get DMPS and CaEDTA.
Lots of mercury and other heavy metals have come out.
One is very toxic she's the more severe one she excretes mercury in the extreme levels.
The other one has excereted in the extreme levels as well but she's high functioning now and just does rectal chelation.
My other one was doing rectal chelation but for her she wasen't excereting as well so they have been doing the IV chelation and rectal 2 days following..
and she gets her chromium selenium zinc glutathione vitamin c ect with it as well.
They brought up trying IV chelation with my other daughter to excret better but as she's pretty high functioning now..
I thought we would just stick with it this way now.
The other one seems to be more impacted at this time so we are focusing more on her..
We got a late start as they where born in the 90's and doctors ect weren't to much up on autism back then it was hard to get a diagnoise.
And they really seemed more focus on learning/pec's and behavioral therapy back then..
So we were pretty much into that path untill I found out about the mercury ect in thoses shots they had.
I feel like we are doing the right thing now but I wish we did it sooner as we wasted alot of time trying to figure this thing out but...
I asked the doctors office why not DMSA and they said that it's stronger harder on the system and I know it's hard enough on my daughters system now.
Though she doesn't seemed as bothered anymore since they don't have to sedate her anymore.
The sedation cause her aggravation but without it she's been much calmer now following.
But she doesn't need stronger being she has a high mercury count.
My daughters got it from their Vaccines..
I'm totally convinced of that that their bodies retained all that Mercury and Aluminum that I see comeing out of them now.
But you said...

Quote
genetic mercury poisoning? meaning I got it when I was in the womb, passed down to me by my parents.


How did that happen? Where did they get the mercury from?
Did they both have mercury fillings in there teeth?
Eat tuna while pregnant? Used a product that contained mercury?
Any history of grandparents family members useing thoses teething powders that caused pink disease?
Work in an industry that works with heavy metals?
How did you get poisioned in the womb??
Have you ever got flu shot's or any vaccinations yourself?
Did your mother get any while pregnant Rho gram ect..
Any fillings in your teeth?

What do you think it could be or does the doctors really know?

Thanks
Lynn


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