wanting other's using ldn 4 m.s. to share their thoughts on this please

[Guest guest]

I am freaking a bit over this post.....I have been taking LDN 3 mg for

about 2 years and it has been OK until about a few month ago.

I started getting worse: numbness, tingling, weakness. I started taking

4.5 LDN and start feeling improvement.

Neurontin and hormones were also mentioned.

So basically I have worked my way up to 3.8 mg's ldn, at 3 I had

extreme spasms and I make it up from the 50 mg pills so no worry over

fillers. My question - thoughts on if I should stay at this dosage or

continue on my ldn journey to the 4.5? What if I am at my dosage and

need the increase to 4.5 in the future? I am doing so well on the ldn

that I have stopped my shots of Copaxone a little over a month ago.

My brief history is I'm 4th to be dxd with ms in my family, spasms so

severe that my former neurologist brought up the Baclofen pump cuz

doses of 140 mgs daily of it were'nt working, I refused so he said he

wanted to cut the tendons in my legs. Again, I refused. I use

stretching, deep breathing, and meditation to control them now with no

medications. Glad I don't listen. I am still walking btw.

Any thoughts greatly appreciated.

Warm regards,

Donna