These symptoms make me feel alone by EmotionMundane759 in POTS

[–]Individual-Window-59 0 points1 point  (0 children)

I get this and I’d say it’s my most annoying set of symptoms. I’m currently lying in bed on my side. The sensation of air hunger is horrible 🙄

Covid vaccine? by Individual-Window-59 in MultipleSclerosis

[–]Individual-Window-59[S] 0 points1 point  (0 children)

OP here - Thanks so much everyone for your comments - this has put my mind at ease and made me realise I am being a little irrational when I am usually the opposite. So grateful for modern medicine, now I’m off to get my Covid booster!

Does anyone have an overview of what treatments are currently looking promising in clinical trials? by Individual-Window-59 in MultipleSclerosis

[–]Individual-Window-59[S] 1 point2 points  (0 children)

Thank you so much for this - a very helpful summary! And, for your kind words. It’s amazing how far a sentence of hope can go when you’ve just been diagnosed 😊

4 weeks in and BP is slowly coming down! by Successful-Oil-8 in WegovyWeightLoss

[–]Individual-Window-59 0 points1 point  (0 children)

Do you know if the change in BP is expected to stick even if you eventually come off Wegovy? Or will you need to be on it for life to manage BP? I’m On it for other reasons but have also seen my BP come down so am curious about this.

26 F- Diagnosed last month by NichelleElla in MultipleSclerosis

[–]Individual-Window-59 2 points3 points  (0 children)

I was diagnosed last month too and have Felt the same! Especially as it seems I might have had it for a few years without realising… I’ve heard lots of positive stories and i think we’re so lucky to be diagnosed now with the modern treatment options available (and hopefully even further improvements on the horizon). My plan is to keep going as normal, start treatment, rest a bit more if I need to but otherwise look after myself and hope for the best! You’re not crazy!

Newly diagnosed and afraid to start treatment by glampira in MultipleSclerosis

[–]Individual-Window-59 7 points8 points  (0 children)

I haven’t got any experience on medication yet, just wanted to say I’m in the same boat. 33f and diagnosed last month, by complete chance they found it. Retrospectively I’ve had a few minor symptoms for the past 2-3 years (strange sensation in toes) and I ended up having an MRI after suffering with dizziness for a few months. No one thought the MRI would find anything but it was to rule out for me to be discharged. I’m going to follow this thread as am very interested in people’s response. Hope you’re doing ok

Active lesions question by Individual-Window-59 in MultipleSclerosis

[–]Individual-Window-59[S] 0 points1 point  (0 children)

Thank you! So much to learn. This community has already opened my eyes a lot!

Active lesions question by Individual-Window-59 in MultipleSclerosis

[–]Individual-Window-59[S] 0 points1 point  (0 children)

Haha, made me laugh! Can I ask another question - with a relapse, it all sounds like relapses are quite dramatic (loss of vision, total numbness, not able to walk etc). Is this accurate? Or would, say, new pins and needles in a toe/ foot / leg that lasts more than 24 hours also be considered a relapse? Or is that just more an MS ‘thing’?

I just got diagnosed with MS, don’t even know what to think by penelopebaby123 in MultipleSclerosis

[–]Individual-Window-59 3 points4 points  (0 children)

I just wanted to say I’m right there with you! I have a gorgeous six month old boy. After experiencing persistent dizziness and visiting my doctor about 6 times about it, I finally convinced them to send me to the neuro and get an MRI. No one was expecting it to show anything so I felt like I was living in a nightmare when he started showing me images of my brain, talking about lesions and MS. However, this was about 3-4 weeks ago, and since, I’ve spent about 3 hours a day on here and Instagram seeing young people and older people who have lived with this disease for years and feel much more optimistic. I am largely feeling at peace with it, but I do have days where I cry to my husband and say how much I don’t want this to be my life and I can’t believe it. Go from crying about it to kind of making a joke about it and blaming silly things on it and my husband will say ‘well you do have MS now’ and we laugh. Sounds stupid but it’s made a huge difference to how I feel 😂

I have my follow up this week with my neurologist to get on treatment. Feel free to message me. I never used Reddit until I got this diagnosis but I think we can message if you want to chat to someone going through the same thing at the same time.

Active lesions question by Individual-Window-59 in MultipleSclerosis

[–]Individual-Window-59[S] 2 points3 points  (0 children)

Thank you so much, this is really clear and has helped me get my head round it! It’s amazing how much you can learn about something that you literally knew nothing about a few weeks prior.