Disclaimer: This page may contain affiliate links. We may earn a small commission for purchases made through links in this post, at no extra cost to you.
4 months on LDN
by Steve W.
(Tasmania, Australia)
I have had MS for 14 years, went from RRMS to SPMS about 4 years ago, which is when I really started to go downhill, now in a wheelchair. Have not taken any medications other than IV Methylprednisolone occassionally.
Started LDN 4 months ago, now 4.5mg nightly. Have not had any side-effects or seen much in the way of symptom abatement. However I'm mainly taking it to arrest the progression of the disease. I've found I have more bowel and bladder control and if it does no more than that I'm happy.
Dear Friends,
"Life in Spite of MS is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com. We're also part of the Ebay Partner Network, another affiliate program."
We'd also like you to know it doesn't cost one cent more when you click through the links here on our blog. Not one single penny. And we will make a little extra cash when you do click through. We'll be ever so appreciative. You also have our word that we'll only link to things that we would use ourselves, (or wish we could have or use).
Sincerely,
Cir & Akrista
You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!
Privacy Policy ~ Advertising Policy ~ Disclaimer ~ Contact Us ~ About Us
