← Return to Severe Sensorimotor Polyneuropathy, Muscle Wasting, Numbness

Discussion
Comment receiving replies
Profile picture for annasonery @annasonery

@moorethrpy Thank you so much ♥️
He is a real fighter and I hope things keep improving. I don't know what is it about movement but so many positive things happen when we move. We are not made to be stationary beings.

As for K lasted therapy he did not try that yet. Is it any good?

From therapies at a clinic he only does NMES - Neuromuscular Electrical Stimulation and he says it helps him a lot. He does that once a year for few weeks.

There is also some exoskeleton which I got him from amazon and it helps with spine posture and he swears by it. He also told today that he tried Carbon Fiber AFO for ankle support and said it helps him walk even better.
There are many things that patients can do which can help them but as I said in previous post you have to do multiple things from different angles and results will come ♥️

Bless you

Jump to this post


Replies to "@moorethrpy Thank you so much ♥️ He is a real fighter and I hope things keep..."

@annasonery Totally agree..a multi prong approach. I also take a prescribed vit B supplement so that I get the appropriate amounts. I go to gym for classes daily...movement is so important. I will let you know about Laser..I see Chiro tomorrow. thanks for sharing.so much of our adaptation is not feeling alone and learning from others.