Summer heat and MS don’t mix . Try to find some cool air for awhile Kaylee

INVEST IN SMART PLUGS & Smart fan so u can control with your voice will help with the heat and try some exercises for the numbess... that worked for me

I would ask to have a nerve conduction test if you haven’t already. From your additional information you say nerves are involved, so definitely tell your neurologist you need to have this test done. Be your own advocate! It’s the only way to get things done.

My Dr. would prescribe a blister pack of prednisone for 6 days. That took the inflammation down and got me back to normal, well back to my normal.

Hi Kay
Maybe not MS symptoms per se. I'm PPMS and as my condition has worsened and I've gone past being able to do proper cardio exercise, my muscles have deconditioned (atrophied). I get lots of pain in my lower back, hips, sacroiliac joint, glutes & thighs but regard it as a comorbidity. Affects walking and standing significantly but is a MSk (mussculo-skeletal) issue rather than neurological.

Does that help / can you relate to those sensations?
Graeme