Re: morgellons website free information regarding causes and treatments

Weak post Phanta.

Since our syndrome has been labeled as imaginary by the medical establishment, we rely on anecdotal accounts of treatment experiments by sufferers to get better. If a recently infected Morgie could only go to 2 websites to understand their affliction, would you tell them to go to the CDC and Mayo Clinic website, or the anecdotal forums at lymebusters and curezone?

My life was turned around - 40 symptoms reduced to 5- when I decided to follow the advice of a laysufferer who convinced me to take massive doses of vet meds that are not approved for use in humans. I doubt that these anthelmintics effect bart bacteria, though it's plausible that bart is the deepest root of my issues.

I think your suspicions of bart involvement are justified. But you must remember that, at this point, it is just a decent hypothesis. The few doctors and researchers that recognize Morgellons often specialize in lyme disease. So they are reasonably educated in bart diagnosis and treatment. They are wholly unconvinced that bartonella is the cause or even present in most Morgies. (Source: CEHF conf. 2014 DVD). It's wrong to ask Maybelle to remove her website based on lack of scientific proof, when your bart/morg connection lacks the same.

Maybelle is a noob around here making excellent contributions. Her candid posts about contagiousness are more accurate than posters who have had this for decades IMHO. Her site is off to a good start, and I appreciate the attention to rotifers, magnesium, and salts.

Your posts work so hard to exclude other's theories from your own. I think you should be exploring how they might relate to your own discoveries. How would EMF pollution, rotifers, nematodes, recreational stimulants, and solvent/pesticide exposures interact with the bartonella bacteria?