Hello lovely people 😊
Hi all, new to shift ms. I was diagnosed in 2017 with RRMS. I tried a few DMT's but was 3rd time lucky with Cladribine (mavenclad) I'm now going into my second year pill free and so far so good, I still have new lesions but they are much fewer and I've not had any major relapses since beginning Cladribine. Since being diagnosed I have slowly lost friends and hobbies my life has changed dramatically and I struggle to cope with this change every day. I've lost who I was and I don't know where to start making new friends (real friends) and what to do with my life I've hit a bick wall. I don't know if anyone has felt this way or feel the same? Anyway, I hope you are all keeping safe and well.
Hi @Chelle82 welcome I’m new here as well. I feel like I wrote that it’s sad to realize who your true friends are when you are diagnosed with a life changing autoimmune disorder. Thankfully your family and true friends stick around. Here is a good place to make new one’s that you can actually relate to and know they know what you are going thru. So welcome again and feel free to message me whenever you want. Enjoy your Friday 🤗
Thanks @marychvz7 have a lovely weekend 😊