LDN & Neuropathy

[Guest guest]

Good morning,I have been fighting multiple myeloma for a little over nine years now. A couple of years back, my oncologist put me on the horror drug of the 60s THALIDOMIDE to treat the myeloma. It did a good job for almost two years, but then I noticed that I was losing sensation in my fingers and toes. We stopped, but the damage had been done. I now have what I would describe as a pretty horrible case of peripheral neuropathy to add to my cancer. Two weeks ago my wife started LDN for MS. I actually found out about LDN through a web newsletter called Cure Your Own Cancer. That led me to this group, where I see folks chiming in about both MS and cancer. So, we got her started and are moving forward with guarded optimism. The Avonex and Rebif kits went into the trash, we found a good compounder here in land, and I am to the point where I think I'm ready to get going with LDN myself. I have noticed several group members writing about LDN and fibromyalgia. The thing that disease shares with peripheral neuropathy is discomfort and pain. I'm wondering if, in addition to treating the myeloma, I might get a spinoff benefit from the LDN for my peripheral neuropathy. Just kind of wondering out loud if anyone in the group has any familiarity with PN and would have any opinion of LDN's impact on it. Hope to hear from anyone who does. Have a great day. I am inspired by this group every day! Quite a bunch of determined and uplifting folk you are.-Al Can a Web portal forever change your life?Win up to $25 Million on iWon - click here!