Hi,
I’m in the older group of people diagnosed with PPMS - I’m now 62 and was diagnosed 5 years ago.
My mobility has deteriorated from no aids initially to stick - rollator and now wheelchair for long distances.
Would love to chat to someone in similar position and also I’m really confused re meds - was told initially no dmd but now being offered meds as they now think I’m having relapses so I may have primary with relapses.
Very confused and unsure what to do.
Is there anyone local who can chat or support group near me?
Thanks x
You might find something suitable here.
Support near you | Multiple Sclerosis Society UK (mssociety.org.uk)