Newly diagnosed
Hi everyone I'm newly diagnosed with PPMS I'm just getting my head around it, i am suffering with constant pins and needles in my hands and feet, can anyone suggest anything I can do to help me cope with this
Thank you
Sandra
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Last reply
Hi, Welcome and yes I find gentle massage can really ease the feeling. It doesnt last, There are medications that can help. Talk to your nurse.
Hi Sandra, I found that using a heat pack and gentle massage did the trick for me. Once I found the correct medication for me, things certainly improved. As Jay (above) said, speak to your MS nurse. Good luck and keep in touch. x