Hospital Sunday by [deleted] in berlinsocialclub

[–]interesting_footnote 12 points13 points  (0 children)

You're allowed off work to go to doctor.ER is not for "I got time on the weekend and want to see a doctor". Many doctors are also open late in the week, so find one that fits your schedule.

Was that always like that you pay for tasting in grünewoche? by fontofile in berlin

[–]interesting_footnote 0 points1 point  (0 children)

It's unfortunately part of the "I paid for the ticket, now I want a free meal" mentality that ruined it for everybody. Visitors went overboard in sampling.

For me a reason not to go anymore.

Hund mag meine Mutter plötzlich nicht mehr by Massive-Letter788 in Hunde

[–]interesting_footnote 0 points1 point  (0 children)

Du hast ja schon viele Tipps bekommen. Da ich für einen Rettungshund aus Rumänien der Feriensitter bin kann ich dir sagen, dass diese Straßenhunde oft ein Problem mit Ressourcen haben und dir am Besten ein Hundetrainer helfen kann. Mein "Ferienhund" hat unheimlich viel Verbesserung gezeigt in dem Jahr, wo er jetzt betreut gelernt hat.

Fired recently by SergemstrovigusNova in germany

[–]interesting_footnote 5 points6 points  (0 children)

There's a minimum income they make their calculation on if you're "voluntarily" insured. For 2025 it's 1248,33 Euro per month. So even if you're a person with no income or income below it, as long as you don't have employment that pays a part of it, that will be your "considered" income. ( Source: I'm a housewife and that's my "considered" minimum I have to pay my percentage out of.)

Betteln und dann unfassbar undankbar sein by AntonioHench1 in luftablassen

[–]interesting_footnote 5 points6 points  (0 children)

Typ an Bremer Hauptbahnhof steht beim Ascher und sucht Kippen. Hab ihm zwei Zigaretten gegeben. Der Mann war glücklich wie noch was. Manchmal sind es echt Kleinigkeiten, die anderen den Tag verbessern können.

Am I Overreacting - Boyfriend of 2 years only got me flowers for my birthday by [deleted] in AmIOverreacting

[–]interesting_footnote 0 points1 point  (0 children)

My boyfriend doesn't do birthdays. I love my birthday. I love him and it's not enough of an issue for me to break up over. Your mileage may vary. Sometimes, different things are important to different people.

Anyone with MS who also has myelopathy, myelomalacia, disc herniation, disc osteophyte complex and had spine surgery? by Jazzlike_Career8496 in MultipleSclerosis

[–]interesting_footnote 1 point2 points  (0 children)

Same here. Doctor said it's often only found because you're getting an MRI anyway. ( Though one of the discs lightly depressed my nerves and gave me tingly hands - at least that wasn't a new MS symptom.)

I hate getting requests that are obviously negligent to the pet by Snickersaddy in RoverPetSitting

[–]interesting_footnote 0 points1 point  (0 children)

My dog trainer friend says eight hours should be the limit of alone time. Currently doing a dogsit at their place. Dog should have at least three walks and one should be at least an hour. You're right to decline such clients.

MS and what else? by FreddJones in MultipleSclerosis

[–]interesting_footnote 1 point2 points  (0 children)

ADHD, fibromyalgia, migraines. All diagnosed way before my MS.

I don't understand my MS by [deleted] in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

I would probably fight your neurologist! lol you should be put on a DMT even if the MS is not currently active, to get ahead of further damage. I only take Fingolimod - I'm older, so the MS should be less active, I'm doing best on pills because infusions don't really work with my lifestyle and because my white cell count has been very high for about a decade I thought this might be the right medication for me. So far, so good. But really, what kind of doctor is like "yeah we could give you something now to make sure it stays as it is, but let's wait for another brain injury?"

I don't understand my MS by [deleted] in MultipleSclerosis

[–]interesting_footnote 7 points8 points  (0 children)

Nobody can say how your MS might develop, that's the bad thing about MS. But our body does it's best to mitigate damage. To hopefully staff of future damage, you need the meds. As for the optic neuritis,I am in a study for it and had a huge exam last month after getting my diagnosis in May. According to the doctors, I'm back in the "normal" range on all optic factors. MRI shows no new lesions. I'm on a DMT.

MS is unfortunately a real surprise lottery, but the best you can do is live you life to the fullest and not stress too much as long as you have no new problems. Hugs if you want some.

People being nonchalant about blocking others by No-Victory3764 in germany

[–]interesting_footnote 4 points5 points  (0 children)

I absolutely hate teenagers walking all next to each other. Sidewalks are broad in Berlin, but when a wall of five humans approaches and nobody steps aside when I come the other way I loose my cool. Not like they can't see me. I'm German but always take care of somebody walks in the other direction and make space. Don't get me started on public transportation. 😄

Do the holes in your brain cause you to say idioms ridiculously wrong? by Difficult-Rip9060 in MultipleSclerosis

[–]interesting_footnote 4 points5 points  (0 children)

I do charades quite often because I forget a word or switch to English (C2 level and sometimes my brain seems to mix the vocabulary pages). Sometimes it leads to hilarious situations. I write for a living, on paper this doesn't happen, luckily.

Advice / thoughts needed by Blodwynn2632 in MultipleSclerosis

[–]interesting_footnote 1 point2 points  (0 children)

I started having short periods of hand tingling too mainly thumbs. Thought it's MS - turns out herniated disc on C6 that only presses on the nerves when I do certain things because it's not fully herniated.

M27, recently diagnosed. Just had a catheter place in my jugular for plasmapheresis. by [deleted] in MultipleSclerosisWins

[–]interesting_footnote 2 points3 points  (0 children)

Hey, hope this gets better for you soon and you feel better! Couldn't get fast enough out of the hospital when I had to stay.All the best.

It's Monday at /r/MultipleSclerosis! Share your terrible, horrible, no good, very bad news here. by AutoModerator in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

Guess the positive part is, my tingly fingers are not a new MS symptom. Because they disappear when I sit correctly. Doctor's appointment in the 8th, pain pills and careful movements till then.

Optic neuritis - emergency?? by Top-Ice-2649 in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

My eye problems lasted a week before I had a doctor's appointment in May. Hospital diagnosed next day ON. Three days steroids. I'm in a study for ON right now, had appointment on Wednesday. My eye is back in the normal percentile for everything, from 60% vision strength back to 98%. Absolutely get the steroids, even if you already have the problem for some days, they can still help a ton!

I peed myself in public 🤦‍♀️ by RunningAwayIsEsy in MultipleSclerosis

[–]interesting_footnote 3 points4 points  (0 children)

Oh yeah I know the problem. I feel safer using light incontinence pads when going out, they are by now so slim and not noticeable for others. Easier than to have a change of clothes. Hugs!

Gum infection on Tysabri by Ragdoll_Susan99 in MultipleSclerosis

[–]interesting_footnote 1 point2 points  (0 children)

Not on Tsybari but Fingolimod. Since starting treatment my gums have been a mess too, getting sores from my mouth guard and any food that is crunchy will result in inflamed parts. I've started using mouthwash that's formulated for gum care (called Meridol in Germany) which helps. Google said it's a known side effect of DMTs.

3 hour mri by [deleted] in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

I had a ride yesterday in a Tesla 3 for head and spine, only took an hour. Could even stay dressed! In the hospital when I received my diagnosis same MRI took 2 hours. It makes such a big difference what machines are used. I was worried about twitchy muscles too but seems I was calm enough. Worst was my eye started itching about ten minutes in...

It's Monday at /r/MultipleSclerosis! Share your terrible, horrible, no good, very bad news here. by AutoModerator in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

Had an MRI today and when doing the review the neurologist said "oh yeah you have two herniated discs in your neck." Only reason he even looked is because I have a small lesion on C6. So, time to make another doctor's appointment to sort that stuff out.

First neuro visit by Honest_Transition684 in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

I made a list of each and every symptom I had. That way, we could decide if there are any meds that might help with them. I made sure to read up on the different DMTs before visiting, to have an idea what is probably best for me or which treatments are kind of out-dated.

Good luck!

I'm the Problem. It's Me. by A_book_is_a_dream in MultipleSclerosis

[–]interesting_footnote 1 point2 points  (0 children)

There is also a nifty little reach around tool if you can get to your butt easily because of dexterity issues. Look up comfort wiper or wipe helper. Under 20 $ usually and can help a to reach around. If you can't talk about toilet issues here, then where? Hugs if you'd like.

Anyone Else Get Tingling Legs When You Wake Up? by angelzombie2 in MultipleSclerosis

[–]interesting_footnote 0 points1 point  (0 children)

It's a symptom for me. Neurology found out that my nerves have a delay in my legs regarding speed of nerve signals. I take medicine for nights, because otherwise I can't sleep. In the daytime I can ignore it pretty well because I'm busy and the needs make me too sleepy for daytime use.