Guest guest Posted September 25, 2008 Report Share Posted September 25, 2008 How was he being treated for lyme? In the movie Under Our Skin one doctor asserts he never met a parkinson or als patient that didn't have Lyme so there is a big connection there. Have you heard of Salt/C regimen btw? It something you can add to whatever treatment you are currently using and it appears to help allot of people. My wife is one of them. You can get more information about it on the lymestrategies list. adams > [ ] Lyme that leads to Parkinson's > > Does anyone have experience dealing with Lyme that leads to > Parkinson's? Is > there a doctor out there that treats patients with this problem > specifically? > > My husband was being treated for Lyme then came down with > Parkinson's or > Parkinsonism. We are searchiong for the right treatment for > him and the > right doctor. > > Ann Prow > annprow@... > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2008 Report Share Posted September 25, 2008 Ann....lowering his total body burden of pathogens and toxins, and working on getting the Mercury/Lead out of his body will work....The Parkinson shake I have had is now diminishing, as I work intensely on getting the Lead/Mercury out of my body.....it is a slow process, BUT IT WORKS.... My getting rid of the Mercury/Lead will also help the Lyme....Lyme critters feed off of heavy metals.... You can go to www.gordonresearch.com and type in these words in the search box....You can't get into FACT, but I can however, I'm sure that the main search box will give you a ton of reading.... Angel Huggzz or Angel www.lymecommunity.com " stay tuned " for the exciting Lyme Conference here in June 2009....We have the hotel, which is chemical free.... [ ] Lyme that leads to Parkinson's Does anyone have experience dealing with Lyme that leads to Parkinson's? Is there a doctor out there that treats patients with this problem specifically? My husband was being treated for Lyme then came down with Parkinson's or Parkinsonism. We are searchiong for the right treatment for him and the right doctor. Ann Prow annprow@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2008 Report Share Posted September 25, 2008 I'm glad Salt/C worked for your wife, . It put me in the hospital, and it took over three months of strict bedrest for me to even get back to where I was. I'm just saying: it's something people need to be very, very careful with. It turned out later I had a common-enough genetic anomaly (known as an ACE deletion) that made it hit my body in a way that completely disrupted my endocrine system. A majority of people diagnosed with CFIDS have the ACE deletion, along with other SNPs that also affect adrenal function And since nobody really knows how many CFIDS patients really have undiagnosed Lyme, it seems likely that these problems may be more common among us as well. (I have a friend who is currently researching this very thing, in fact.) The bottom line: Approach Salt/C very, very carefully. If your feet and legs start swelling AT ALL, or your heart starts palpitating, get off it immediately, and don't even think about going back. It's your body telling you it's heading for deep, deep trouble. Sara On Sep 25, 2008, at 10:10 AM, wrote: > Have you heard of Salt/C regimen btw? It something you can add to > whatever > treatment you are currently using and it appears to help allot of > people. My > wife is one of them. > > You can get more information about it on the lymestrategies > > list. > > adams > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2008 Report Share Posted September 29, 2008 Good to know! Thanks Sara! > Re: [ ] Lyme that leads to Parkinson's > > I'm glad Salt/C worked for your wife, . It put me in the > hospital, and it took over three months of strict bedrest for me to > even get back to where I was. > > I'm just saying: it's something people need to be very, very careful > with. It turned out later I had a common-enough genetic > anomaly (known > as an ACE deletion) that made it hit my body in a way that > completely > disrupted my endocrine system. > > A majority of people diagnosed with CFIDS have the ACE > deletion, along > with other SNPs that also affect adrenal function And since nobody > really knows how many CFIDS patients really have undiagnosed > Lyme, it > seems likely that these problems may be more common among us > as well. > (I have a friend who is currently researching this very > thing, in fact.) > > The bottom line: Approach Salt/C very, very carefully. If your feet > and legs start swelling AT ALL, or your heart starts > palpitating, get > off it immediately, and don't even think about going back. It's your > body telling you it's heading for deep, deep trouble. > > Sara > > Quote Link to comment Share on other sites More sharing options...
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