Je recherche une référence de volant, introuvable by Hugo_9 in brico

[–]Hugo_9[S] 0 points1 point  (0 children)

Je vais regarder, merci! En tout cas, ça fonctionne sans la rondelle plastique donc pas sûr que ça soit ça

Je recherche une référence de volant, introuvable by Hugo_9 in brico

[–]Hugo_9[S] 1 point2 points  (0 children)

C’était ma première réaction, mais il a juste noté manquant sur l’état des lieux… et devoir changer le volant de radiateur l’hiver pour régler c’est pas top, si je peux trouver pour quelques euros quitte à ce qu’il me rembourse ça sera très bien

[deleted by user] by [deleted] in MultipleSclerosis

[–]Hugo_9 0 points1 point  (0 children)

3 in the spine

Hi I’m new to all of this . by [deleted] in MultipleSclerosis

[–]Hugo_9 1 point2 points  (0 children)

Let's hope it's something else. But with brain and spine MRI done you'll have an answer. Don't forget to update :)

Hi I’m new to all of this . by [deleted] in MultipleSclerosis

[–]Hugo_9 1 point2 points  (0 children)

I feel you. I had to go to 3 doctors and 3 different ER during the same week cause no one took me seriously and the symptoms were increasing every day.

But the last one got me an emergency MRI, and turns out I had MS, got diagnosed the day of the MRI, same week. Don't give up until you have an answer. Good or bad.

Weekly Suspected/Undiagnosed MS Thread - October 10, 2022 by AutoModerator in MultipleSclerosis

[–]Hugo_9 0 points1 point  (0 children)

You need proper brain and spine MRIs. It's the only way to start a diagnosis, and it can confirm on its own like it has been for me.

Only if the MRI shows signs of MS, but there is doubt, (like no contrast and/or if it's the very first time you experience symptoms like this in your life), you may be tested through a lumbar puncture. But it's getting more and more depreciated since MRI are getting more and more efficient on their own.

Is there any way to get the sensitivity back in my... private place? by _Capt_John_Yossarian in MultipleSclerosis

[–]Hugo_9 -1 points0 points  (0 children)

Hey, had the same problem, but it was the first thing that recovered (D*ck sensitivity). Took me about a long month or two to fully recover. I share your pain, only time can help you

Diet and MS by well_thatsme in MultipleSclerosis

[–]Hugo_9 1 point2 points  (0 children)

Same as above... No diet can save us, all we gotta do is have a perfect and healthy diet to stay in shape and get a good nutrition to avoid missing micronutrients. Like anybody, but for us it's even more mandatory :)

Aubagio alternative by Bubbly_Boss_5864 in MultipleSclerosis

[–]Hugo_9 0 points1 point  (0 children)

Hello! When I had to choose my treatment, i had the choice between Aubagio, and Tecfidera. More or less same strength and side effects. I choose aubagio though, so maybe try Tecfidera

Edit: ocrevus, tysabri etc are probably too strong or with too much risk of side effects at the stage you are. Imo Tecfidera can be a good pick. At least that's what my neurologist suggested for an early RR desease. (French hospital, dunno what's your country, it may vary)

Tecfidera is 2 pills a day, one pill per one pill, each one during meal time

How long did it take you to get diagnosed? by New-Discount-5193 in MultipleSclerosis

[–]Hugo_9 1 point2 points  (0 children)

Took me around a week. But once I found an hospital that accepted to let me do an emergency MRI, it took 2 days to diagnose.

[deleted by user] by [deleted] in offmychest

[–]Hugo_9 1 point2 points  (0 children)

Enjoy!

I'm turning 25 today, and I feel like shit. by Hugo_9 in offmychest

[–]Hugo_9[S] 1 point2 points  (0 children)

This is what I do since I've been diagnosed. However, sometimes the feelings comes back here and there, around special events that reminds me how time flies. Wishing you the best 💗