@MrsKing 

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MrsKing

New Aussie

Hey guys, this is all new to me, I don’t even like to talk about the fact I have MS, I was diagnosed April 2018 after most of my body went numb (all better now tho) I guess i just want to say hi, I live a relatively normal life these days I suffer from fatigue and dizzy spells but otherwise I think I’m doing ok. My muscles ache especially in my back and neck a lot and I get niggling pains all over my body. Doctors just shrug all my complaints off and my neurologist while positive doesn’t really explain much to me most of what I no about my illness I have found on google. I am probably still in denial over the whole thing to tell you the truth. I have ocrevus every 6 months and that seems to be doing it’s job so I’m happy to continue with that, otherwise I just take it 1 day at a time and just hope my attacks stay away and I can live my best life with my two little girls and amazing husband. I look forward to being Abe to get insight from people who actually no what I’m going through. Cheers everyone x
@RMDaniels

@mrsking Welcome & thanks for sharing a bit of your journey with us! It’s very positive to hear you’re doing well with Ocrevus. I’m considering switching from Tecfidera to Ocrevus. Like your experience, it seems like my neurologist is reluctant to give me much information! I’m totally surprised by the lack of communication. This has been a GREAT place for me to find out more about this beast! @stumbler @highlander @dominicks are always posting links to great articles from the most reliable sources that I’ve found very helpful! I wish you all the best!!!

@MrsKing

Hey there @rmdaniels thank you for your reply It’s nice to no I’m not alone with all this! Sometimes it feels that way! Thank you for the info I will keep an eye out for the links. All the best to you to! X