What state do you live in?

[VenusFlider]

Dallas, Texas here!

I am new to the forum and live in Dallas. I have been struggling for a year and a half with this and have started isolating myself for fear that my family and friends will catch it (my dogs now have it). Is there a social group or event we can reach out to one another? It is definitely getting a little lonely

[VenusFlider]

I am definitely interested in any information you guys have about doctors located in Dallas or Texas that are trying to treat this or at least acknowledge it. My experience so far with 6 doctors was humiliating and a waste of money.

[chocket]

Hi Folks,
Im back! I was one of the original 100 people used in the survey the CDC, Armed Forces Division of Pathology and Northern California. I recently moved to Connecticut and am looking for anyone who might be a least a bit sympathetic to what I am going through. Also, in California at Northern California Kaiser I found a wonderful compassionate physician. Her name is Dr. Rose, dont mistake her for her husband that works in the same office. If you live there and belong to Kaiser, try her out. Just dont come on too strong and call it 'Unexplained Dermopathy'. Cheers, Carrie

[scabdraggr]

A cat is a cat and a dog a dog.Unexplained derm is UD.So what does she call it,DP?It sure is unexplained and affects the skin.Maybe fibermyasis or scratch fever!I don't get it.Stop visiting drs and save your money.Many good treatments here while we wait for the division of pathology to decide how to use this for a bioweapon or how to avoid telling us the truth.I feel certain that they know what is happening and what causes it.I can treat myself and I have made great progress but I know that nothing so far can chase it from the small intestine and the prostrate gland.

[brighterdays]

Is anyone else here from Dallas? Did anyone find a medical professional willing to help?

[jonsi]

Hi chocket, did the pharmaceuticals help you in the long run?

For me, homeopathic/natural medicine works.

I'm in northern New Mexico, Jemez Mountains.

itwl,
~jonsi

[Marle]

I found this site from a link in Lymebusters.I posted regarding my state long ago...Seattle WA, USA

[gapey]

Hi Marle and everyone! I'm in the Seattle area too. I've pulled a few fibers from my face over the past year which led me to believe it may be Morgellons. I don't have any open sores or any problems with itching. I hope it doesn't progress to that. I have been dealing with Candida though and just started a candida diet and taking a lot of supplements for the past couple of months and am hoping that will help with this too.

[IWishIwasCrazy]

I'm new here and I live in Tennessee.

[PeacockMaiden]

I live around the Sacramento area.