Only diagnosed

Hello everyone. I have just been diagnosed with RR MS. I dont really know how to feel about it tbh. I have the mind set that. Life goes on but finding it hard to get my head round it. I am so lost as to what to do next. So any help or advice would be much appreciated.

Are good places to start looking. I was lucky that I knew someone with MS for more than 20 years. So acceptance was much easier and I had someone to discuss things with. We each have our own story to tell and for some things progress slowly, for others not. Keeping active and doing as much as possible is the only advice I would give. Concentrate on what you can do rather than regretting what you might not be able to do.

I was a late developer so I only had to cross things off my post retirement bucket list.

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Thank you so much for the links to the information and your personal advice :blush: