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Lyme Disease Support Network

Looking for help


#1

I’m sure I am in the same boat as many others but having suffered for over 20 years without a diagnosis I have finally found out what I believe to be the cause of symptoms which have turned my world upside down. I do not have much faith left in the medical profession so I am looking for any advice on alternative therapies - in particular, MMS and colloidal silver. Any advice is gratefully received. My symptoms are fairly typical of the standard list although I also get a strange tingling over my upper back - especially at night. Thanks in advance


#2

Hi Foxy, I’m sure you will get some responses here but you can also look under the “Complimentary Therapies” category on the discussion wall.

Meli from Mod Support