This is topic Beginning amalgam removal kicking and screaming in forum Medical Questions at LymeNet Flash.


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Posted by Rene (Member # 4870) on :
 
Hi All,

After 8 years with this illness and trying every treatment under the sun, its time to have my fillings removed. The problem is my attitude.
Believe I have reached a point where I do not believe removing fillings will do anything.

I dread the chelation and the illness that this will bring on. Just need to vent and know that I should be more excited. Only feel dread. Thanks for listening.
 
Posted by seibertneurolyme (Member # 6416) on :
 
Not everyone has the same experience obviously.

Hubby had his amalgams taken out prior to his tickborne illness. His main symptoms were nausea/dry heaves and Parkinsonian tremor.

For him the chelation made him feel so much better he didn't mind the hour or two of headaches when he took various chelators.

He did IV push DMSA and for him that med stopped all his symptoms for a couple of days in the beginning. Then as he continued the good times lasted longer. Instead of doing weekly IV's he eventually decreased the treatments to monthly.

When he became sick with tickborne illnesses he initially thought he just needed more chelation because his main symptoms were again nausea/vomiting and Parkinsonian tremors. He had not stopped treatment but was at the once a month phase at that point.

We tried more frequent chelation and consulted several more specialists and his mercury tests were no longer elevated. And the chelation treatments just made him feel bad and did not relieve symoptoms as in the past.

It took over 2 years to get a diagnosis of tickborne diseases and about 3 years before he got any treatment for those.

I am sure he would say that he just wishes he had a mercury problem now as that was so much easier for him to treat.

Hubby ended up with 6 fillings and 10 crowns so he did have lots of amalgams.

Good luck.

Bea Seibert

Editing to add -- Hubby did IV DMPS -- DMSA is oral and he did that as well -- but the IV chelation was with DMPS.

[ 04-05-2012, 05:54 PM: Message edited by: seibertneurolyme ]
 
Posted by willbeatthis (Member # 31111) on :
 
Dear Rene: I think we all reach this point

throughout this journey and yours sure has been a

long one. I think the key with this illness is

to work on all of the things that contribute to

the landscape of Lyme and making our own immune

systems stronger. Getting rid of your fillings

is one of those things. Bea added some great

information as always about chelation and I have

no expertise here. I am doing heavy metal

chelation with my doc and I do find Dr. K's

chelation protocol very helpful. If you do a

search GiGi

writes a lot about it and I think he is very good

at all of this. By chance, have you read

the book by Bernie Siegel Love Medicine and

Miracles... well, that book has helped me so much

on an emotional level with all of this. Granted

I am only into four years of treatment... I can

identify with not having hope. That book made

me hopeful as well as the amazing support from

this group of dedicated people... I can't

imagine this journey without the support. I hear

you and I will be praying for you that you feel

that hope I am talking about. We are here for

you...
 


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