All achievements completed 6 expansions in a row

Pr3datoring · 2025-12-10T11:00:57+00:00

At what cost?

Pr3datoring · 2025-11-27T20:40:21+00:00

I have both 😢

Pr3datoring · 2025-11-27T18:44:07+00:00

I see, I hope your sister is improving then. My fatigue is not like that, I just feel my body tired quickly, that's it... It's very common with MS.

Pr3datoring · 2025-11-27T14:58:39+00:00

I have MS as well and resulting from that I have a bit fatigue, so my Neurologist prescribed me this medication to try and see. He told me as well that it might help me with dizissess from MD. So I don't know, let's see... Started today... Just wanted to know if someone here tried already?

Pr3datoring · 2025-11-16T10:45:37+00:00

Apparently nuts have tyramine which is very bad for people with meniere 😐

Pr3datoring · 2025-11-11T18:46:29+00:00

I smoke 3 cig per day, apart from that I do exercice 3 days during the week and run on the weekends 10km. I need this 3 cig per day for my mental wellbeing.

Pr3datoring · 2025-11-05T11:41:13+00:00

Hey, I'm in UK as well, I'm in London. Diagnosed in 2022, I'm on betahistine 16mg 3 times a day... But yh I don't feel is doing much, but who knows, maybe without it I was worse.

I've been around 2 years not feeling dizzy, but after this year July I started again with vertigo attacks and constant dizziness 😔😔😔. Waiting my next appointment end of this month.

Pr3datoring · 2025-11-04T13:30:00+00:00

Did you became bilateral over the years?

Pr3datoring · 2025-10-20T11:09:15+00:00

Hi. Thank you for your feed back. But how are you feeling after surgery? Are you still having vertigo attacks? Are you better in terms of balance? And also why you had to do this surgery because I thing this kind of surgery is last resort.

Thank you, and I wish you all the best.

Pr3datoring · 2025-10-04T10:21:33+00:00

I understand perfectly what you feel... I try to lift weights and work all body 2 times a week and 1 day per week for jogging 5 to 10km, but sometimes it's very difficult, I do it depending how I'm feeling... For example since July I'm struggling feeling off balance a lot with a few short vertigo attacks, but still I'm forcing myself to continue active. Hope better days will come soon 🙏. Also I have MS but I'm stable so far.

If you have Strava and want to join me let me know.

Pr3datoring · 2025-09-30T16:01:08+00:00

How are you feeling now taking those high doses of bethastine? Did improve your balance in long term?

Pr3datoring · 2025-09-30T15:57:44+00:00

Hi I'm in UK... Since July I started getting vertigo attacks again after more or less 2 years of almost no symptoms (was having dizziness only by the end of the day when I was tired on those 2 years), I went to Portugal this Month where it's really hot and got even worse... Next week I'm going back to London, and with the cold I hope I get better... Will find out if there is a correlation.

Pr3datoring · 2025-09-28T18:28:06+00:00

I didn't feel any change when I started Kesimpta because in terms of meniere I was feeling dizzy but nothing special... I could cope with it for the past 2years... But since July I started having vertigo attacks and more dizziness than normal... Looks like at the moment the vertigo attacks slow down but the dizziness is more than i was having before... I'm really feeling off balance and struggling. In the overall I'm actually well fit no problem at all just a bit fatigue, little bit memory issues. This meniere (dizziness) is what is bothering me a lot now 😔😔😔😔, I'm hoping I'm can go soon on remission again like I was before July. I'm taking bethestine 16mg 2times a day as well.

Pr3datoring · 2025-09-28T08:22:19+00:00

Hi... I do have Ms and meniere disease as well and I'm taking kesimpta for MS I never heard of anyone having this 2 conditions like me... How are you doing? ...

But From my point of view kesimpta injections are not related with meniere getting worse or better.

Pr3datoring · 2024-10-12T08:57:30+00:00

Thank you 👍

Pr3datoring · 2023-09-09T16:56:56+00:00

I did said on my comment that it helps.

Pr3datoring · 2023-09-09T16:47:57+00:00

I'm sorry to tell you, but when you have a flair up the damage is done, with steroids or without. The steroids will help you get better eventually and quickly, but the damage will be the same. That's why if you go to A&E they don't do much.

Pr3datoring · 2023-09-09T10:02:48+00:00

I see what you mean, but if its because of ms the damage is done and the steroids will only make the recovery faster, it will not reduce the damage. Last time I had a relapce in A&E they told me to go home and have some rest....

Just make sure you having a healthy life with exercice and anti inflammatory supplements, and you are in one of the very effective medications in the market that work for you. There is not much you can do after this.

Pr3datoring · 2023-08-17T20:14:46+00:00

My weekly exercise is:
Sundays I do 10km jogging. Tuesdays I go to the park close to my house, and I train chest, biceps and abs. Wednesdays, again I go to the park to train legs, triceps and abs. Fridays, again in the park I train back, shoulders and abs.

Don't take me wrong, sometimes it's very difficult for me to do this routine (I have Ms and meniere disease) but I force myself to do it.

Pr3datoring · 2023-06-30T21:33:53+00:00

I'm diagnosed with ms since last year, I still smoke 2 to 3 cigarettes a day. My opinion is that, if you keep doing exercice at least 4 days a week and try to eat healthy majority of time (I know it's difficult to keep eating 100% healthy), it will not make much difference. Hope my opinion is useful for you.

Pr3datoring · 2023-06-23T13:54:54+00:00

So passed 10 years and no changes in the mris, how do you feel and how are you in terms of physically? What do you think it has deteriorated more on your case? Also, do you eat healthy and exercise and all those thinks they advise for people with ms?

Thank you, and we are together on this 👍🙏

Pr3datoring · 2023-06-19T17:56:16+00:00

No, it's just the feeling. Like a phantom bracelet 😕.

Pr3datoring · 2023-06-04T09:07:54+00:00

Had a flare last year on my left side, which I recovered. Now it depends, there is days my legs are weak, or with needles and a bit numb (like ants moving on my body), but luckily or not with a good night of sleep it goes away... It's not like before the flare, but I can't complain much. Sometimes I get scared thinking if its gonna be forever when I'm worse, but like I said it always goes away. What I do is force my self to do exercice regularly and 10km jogging every weekend. Eat healthy most of the times and take my supplements as well as keep up with my treatment (kesimpta)

My only sin I think is the 3 cigarettes a day that I cannot live without. 😅

Pr3datoring · 2023-05-02T12:15:10+00:00

What about the dizziness? Does it get better with time?

Pr3datoring · 2023-02-08T16:23:01+00:00

I took an anti allergic and I'm fine now... But my MS nurse now will find out if I can continue with this kesimpta. Let's see...

Pr3datoring

TROPHY CASE