J replied: "Hello~
My daughter was prescribed LDN but never had an opportunity to take it...However many other Lyme patients we know have taken it and done very, very well with it..helped the sludgy cognitive issues and the severe fatigue!
(As you probably already know, many to many MS symptoms are identical to MS but almost all treatments are the opposite, save this one and some other brain fog ones)
BTW, have you recently explored the relatively high possibility of Lyme induced MS? If not, please see the following science based web sites (can't hurt to look and process):
Or:
The following websites explain why neurologists do not understand Lyme induced MS (Fraudulent guidelines by IDSA and the AAN was right there with them!!!)-(Anotherwords, it's not the individual doctors, it's the guidelines they must abide by and blindly believe in)
I hope I have not aggravated you...not meant to , just want to bring up to date the viable possibilities.
Best wishes~"
pcheesewhiz replied: "I have multiple sclerosis and I take LDN. Prior to taking LDN I spent my days on the sofa because I had so little energy. I was exhausted all the time and had symptoms that changed every three or four months. Once I started taking LDN, all that changed. I was able to go back to having a relatively normal life. I have the energy to work out at the gym, take care of my home and enjoy a social life as well as working a part time job. My neurologist prescribes LDN to many of her MS patients to manage their symptoms."

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