Hi Folks,

Like most of you know I have the RSD DX by ONLY 30 Neurologists.

I always questioned why?

Just take a look at these photo's.

http://dermis.multimedica.de/dermisr...1/diagnose.htm

I have done nothing short, but fight for my life.

Roz,

Wow, those picture look frighteningly familiar!!!

By the way, what are you doing up at this time of night? For that matter, what am I doing up?

Thanks for sharing. Your message is so very important!!!

Jeanne

http://www.klinghardtneurobiology.com/chemtox.htm

Have a look at what this German doctor is doing in Washington. I've never heard of any of this before. Quite an interesting approach some of which is a bit out there, but worth consideration.

MsL

Hi Jeanne,

I took a long nap yesterday. So I was up late cleaning.

Hugs, Roz

This website has a lot of information about a possible infection connection:

www.robertgschwartz.com

Dear MSL,

I really believe the articles make some very good points. Their is supposed to be a wonderful clinic in Germany. I would love to go, it's like a 3 month program.

My sister in law is German, she says what great wonderful care they have their.

In the States we are a bit in the stone age. Thank You for the article. Much Love, Roz

Hi Jeanne,

The article is great at the very least he is linking inflammation=infection.

I tested neg-for mycroplasma, he speaks alot about L forms in bacteria.

With Lyme alone their are cysts forms, L forms and cell.

Much Love, Roz xxx

I went into Endocarditis due to Bartonella. I just don't want this to happen to anyone else. I had to have IV's for months, I now am able to take Erythomycin.

http://www.ncbi.nlm.nih.gov/pubmed/16388485

Here are some books you can read for free.

http://www.arthritistrust.org/books.htm

thanks for the articles they were great. i have a question that i havent really asked anyone with rsd. have you noticed that since your onset of rsd that you have allergic reations to more med or anything for that fact than compared to before rsd. in my case . since having rsd the only antibiotics that i can take is levaquin vancomacyin and gentamaycin thats it. deathly allergic to morphine even tho at one point i was on kadian for 2 yrs no problems,,its like the longer i have rsd the worse that reactions get . i know that the sympathic nervose system has alot to do with just wanted to know if anyone else has this problem or like my sister says im just a freak a nature lol let me know my pm and neuro and a reasearch dr that i know are doin a study on ppl with scs and the way that the sympathic system works with rsd ie bp heart rate etc