Ireland connections
Although I was diagnosed 25 years ago, its only in last few years that I have been having issues as neurologist says I have moved into SPMS stage. I know everyone symptoms vary but fatigue and balance huge problem at moment. Hard to find support sometimes. MS society have website with classes etc but not as much in rural areas. Any comments appreciated.
There’s a ms group on a app called meetup who have online video chats once a month. Other than that and the ms society’s events I can’t really think of many other places.
Thanks @irish34. You would think there would be more resources by now considering so many more people being diagnosed