Edmunduk
 

I'm thinking of telling my doctor that I think I should have injections. I suffer severe pain in my feet from PN . No treatment so far has helped one Iota! The pain brings tears to my eyes and life is a misery. I'm 85 so would appreciate a bit peace in my life. Hope you get some good results.

We don't have to pay in the UK.

Anyone know of a Stem Cells support group to talk about Stem Cells for joints especially the knees and ankle due to arthritis.

I'm so on the fence for knee replacement and Stem Cells are being talked about more and more. These are not insurance covered in the U.S. and I'm trying to think of ways to come up with the money to do them. So many worries about knee replacement surgery.

And I live with complications from a hip replacement in 2010.

Any inputs and thoughts are welcome. C

Caroline2, there is a group on Facebook called "Infusio Exchange" that is a geouping of people considering or currently having fat-based stem cell therapy; though they are primary Lymes patients. I just happened upon it yesterday but am doing reading and research now. I reached out to ine of the patients who reported healing from SFN...trying to learn more about this and will share my findings.