new with a link

[XhelpmehelpyouX]

Hi everyone I posted somewhere else the following,,,





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Just wanted to say Hi and that I am new. I am from Texas and been having symptoms for a year and a half. Hope to get to know some of you and share ideas etc. Anyhow, I have been coming to this forum off and on for a while now and wanted to post a site that I found online that you all may know of but maybe you don't. Hope it helps someone.

Since I am not able to post a site then you will have to look it up.
clongen . com is a lab. Read on it and morgellons.


I am still learning my way around this place.

[carla]

Thanks and welcome to MDR .
Heres the link .It looks very interesting and they welcome questions.

Morgellons Disease - Clongen Labs

[Sadsack]

Dr. Kilani is working with the MRF as a member of the Scientific Advisory Board. I believe he knows someone with the affliction, and that is how he connected with them.

His lab does a lot of the kind of testing that we are interested in, including Lyme, mycoplasma, and endotoxin testing.

A great resource for us.

SS

[posey]

My D.O wrote me an order for lab test to include:

CD-57 , Mycoplasma , Chlamydia Pneumonia

He was sure to explain to me what peolpe's first initial thoughts are when they here the "C" word but that there are all types of C as there are different types of swallows.

He's so caring and compassionate. He acknowleges "M", knowing full well it is an existing entity.

So, if anyone here is a Dr,. Clinical Lab Microbiologist, Researcher, etc. and is willing or wants to do research or whatever via long distance and via participants Dr., please PM me, I am available. D. O. is also most willing. He does not work for an institution, he is self employed so he is not limited as to what he can and cannot do that is neccessary in helping a patient via lab tests, knowledge , etc. He wants to help those who are suffering in any aspect of their life, regarding med. issues.