Making new friends
Hi all,
I was diagnosed 2001 RRMS tried Avonex for 3 years but could cope with the injections, no further contact with Neurologist and decided just to live life taking LDN. Now back in the system and am SPMS.
I use an active manual wheelchair but can't blame the ms entirely for that - I have drop foot and broke my leg 2019 and had had no neuro physio until just recently. So here I am with wheels.
The wheelchair limits where I can go on my own (environment accessibility issues) so I'm more or less stuck at home. I'm a young at heart, sociable person and miss meeting people, so I'm hoping build some friendships on here. and also find people in my area.....
Good Morning @Bramble1 It’s morning here in Michigan and an easy hello 😄Like you, I had RRMS for years and graduated to SPMS last year. I have 2 rollers. One I use at home and one we take with us. I’m stuck at home as well. Please read my history on this site. I love animals and birds. I have been married to my husband since 2000. My mother was born and raised in France but wasn’t taught French. I used to make jewelry but my dominant hand made it difficult for me along with cooking and some baking. What do you like to do and have affection for? Curious to learn more about you! Cheers! Rochelle
Hi and welcome fellow SP graduate here. Plenty of nice cool people here willing to help feel free to reach out anytime 💪🧡