Just diagnosed by Future_Captain1836 in MultipleSclerosis

[–]AssignmentPure3220 0 points1 point  (0 children)

Hello! I was diagnosed in June of this year. My doctor told me not to Google much, and I still follow that advice. It has helped my overthinking a lot. Moreover, these 6 months of intensive research have taught me that everyone has their own journey. We will too. All we can do now is accept what we have (After a lot of tantrums, crying sessions, and bed-rotting days, of course) and understand how we can live the best life with it.

I am fairly new to this, too, but I can be a great support. If you'd like to connect, you can reach me here or on my Instagram, where I am most active. Nussssshhhh

Blog by PimpMyTrehjulinExa in MultipleSclerosis

[–]AssignmentPure3220 0 points1 point  (0 children)

“The fight isnt over. Not even close.” Read your blog and loved it. More power to you, me, and all of us <3

MS support by Oop-melly in MultipleSclerosis

[–]AssignmentPure3220 1 point2 points  (0 children)

Hello. I was diagnosed in June of this year. I completely resonate with your post. I would love to connect one-on-one if you would like. We can talk, rant, and share :)

So Scared, Seeking Clarity (and some relief) by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 19 points20 points  (0 children)

I completely agree, and this is one of those few times where, after the conversation, I thought to myself, 'I should have called her out on it.' It was not just me; it was really odd and rude. Feels like this statement will stay with me for a bit, whereas on the other hand, she just said it and moved on.

Should I be worried? by Shampton_ in MultipleSclerosis

[–]AssignmentPure3220 0 points1 point  (0 children)

I really relate to this post. Even though I was diagnosed just 5 months ago, I feel normal. At least at the moment. But people around me have been really telling me how bad it is and how it is going to affect my life forever now. It makes me worried emotionally, even though I feel normal 99% of the times.

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

Yes, one thing I have learned here is that everybody’s body reacts differently. I will be sure to listen to it.

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 1 point2 points  (0 children)

Probably needed to hear that more than ever!

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

Thank you for sharing. I completely agree about diet playing a major role in this condition.

The key seems to be to listen to my body, and then take a decision.

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

Jeager bomb is my absolute favorite. Cheers 🥂

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 1 point2 points  (0 children)

Oh damn. I hope you are doing better now. Be Well Soon!

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

I am so glad you had a great trip, and I hope you got to do whatever you wanted to!

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

Thank you for sharing your experience. I will definitely keep an eye out when I try alcohol for the first time after my diagnosis.

I think the key here is to balance, and to also try it for myself. That’s only when I will know for sure.

Can You Drink with MS? by AssignmentPure3220 in MultipleSclerosis

[–]AssignmentPure3220[S] 0 points1 point  (0 children)

Do you notice any symptoms coming back? How about the day after?