Lyme Disease Support Network

Looking for help


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


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