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Old August 9th, 2011, 10:46 AM
sammy is tring to live with m
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Jane, for the ears try some hdrogen proxide 35 percent on qtip. this was one of barakas great ideas and it works. doesnt take much but it shuts them down. sammy
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Old August 9th, 2011, 12:01 PM
marsha is feeling hopeful.
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I totally agree with you that it's not natural. I am leaning towards thinking it has a variety of causes, and some people are more susceptible to it than others. Don't know if it's their body terrain, as I've read about, their immune system, previous exposure to Lyme Disease, chemicals from jet and military aircraft, GM foods, or something no one has thought of yet. OR maybe a combination of one or more of the above.....What I DO know is that it IS and that I have it along with the rest of you. What I don't understand is HOW so many can refuse to acknowledge something that is so easy to see!!!

And I love this: "things were much easier when I was just mental!"
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Old October 17th, 2011, 05:40 PM
lana hakemack has no status.
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I am new to this site.I have had morgellons for 8 yrs. have found them in many stages of the cycle,however no one will look at them but me though a microscope,drs. say Im crazy!Family have seen them! maybe someday a dr. will look.I found a woman on this site called Carla.She says she may have a dr. willing to treat need to find her. Hang on dont give up the battle isnt over yet.
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Old October 17th, 2011, 06:22 PM
tcmgpt13 is "status viatoris."
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Carla has some fairly old lists with doctors for lyme and also for morgellons. These doctors are not found in every state or country and some of them may or may not still be in practice after this length of time. You could also read on this link about how to search for doctors who might help you. Not sure where you live but there are some suggestions on this thread for UK, US, Canada, Ireland and Germany:

morgellons-disease-research.com/Morgellons-Message-Board/general-discussion/4235-finding-doctor-help.html

Another way to find some lyme literate doctors (some lyme doctors treat Morgellons patients) is to search speakers lists from upcoming lyme doctors conferences, such as the one for ILADS which takes place this fall in Canada. Many lyme doctors who are not listed on websites will be listed to show who will be discussing what lyme topic at that conference. Or to find a few of the practitioners who treat Morgellons read about who spoke at the last 4th Annual Morgellons Conference which took place in Austin sometime in April of this year. Information about that conference and who spoke can be found on this link:

thecehf.org/morgellons-disease-conference-2011.html

quote=lana hakemack;84771]I am new to this site.I have had morgellons for 8 yrs. have found them in many stages of the cycle,however no one will look at them but me though a microscope,drs. say Im crazy!Family have seen them! maybe someday a dr. will look.I found a woman on this site called Carla.She says she may have a dr. willing to treat need to find her. Hang on dont give up the battle isnt over yet.[/quote]
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