@StillAsleep84 

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StillAsleep84

How to be an MS warrior...

Hello everyone, I wanted to ask you all what it takes to be a MS warrior? Now more than ever it seems we need to draw on all of our resources and wondered what these are? I'm newly diagnosed, new to this site and looking for some inspiration to help me cope over the next few weeks and months. Thanks in advance x 😉
@katfight

@stillasleep84 For me it's mind over matter but when I get to the point of feeling like I'm drowning I'll talk loads, here is the most amazing place to do that. Read posts that are of interest, keep positive, reply to others or make your own posts. Don't get drawn into the negativity, to many posts are about that can pull you in, don't watch so much of the news either other than what you feel you need to, for me that's Boris Johnsons daily updates. Just know you got this, we are all warriors fighting our own battles with others who get it more than those without ms Be safe and take care 😀

@Lisa_Morghan

Hi I'm Lisa your comment on how to be a MS warrior I'll start with my own personal story my family my Mother my Sister and now me "Lisa" have been diagnosed with MS not fun... so what I have learnt watching caring for them through this is "Stay away from denial " both my mom and sister WOULD NOT tell any one that they were diagnosed With MS. Me I'm still walking I'm on this awesome Site to meet new friends listen read there story... just stay positive be safe and it's okay it really is 🤲⚘✌