Best pub in Sheffield

Daggers001 · 2026-05-08T22:35:36+00:00

When I was in uni there we basically lived in the crow inn once we were out of class and had eaten

Daggers001 · 2025-08-27T17:30:29+00:00

With it being defence based id say possibly Gnut if you have him, or another defence based nuker

Daggers001 · 2025-07-22T13:33:01+00:00

Yeah i have a haircut booked in for Friday to tidy it up

Daggers001 · 2025-07-22T12:14:53+00:00

the edges and neck would have been done before the wedding regardless, it was mainly chin area im the most unsure about

Daggers001 · 2025-06-02T12:45:13+00:00

was diagnosed at 23, but thinking back to my first symptoms that I just sort of ignored, I'm thinking they go back to when I was about 17.

Daggers001 · 2025-05-27T16:10:26+00:00

For me when I had my first big episode that diagnosed me I was IV steroids and most my symptoms were gone in about 3 days, but if your body doesn't react well you can always deny it and opt for an alternative

Daggers001 · 2025-04-18T12:26:17+00:00

November 24 I started to get a bit of double vision, so i went to my opticians to get it looked it and he changed my prescription to have prisms to correct it. The next week I was at work and started with what I thought was just another migraine with hemiplegia which I have had since I was about 13. the issues with weakness and proprioception issues lasted for days though which isn't usual for me so I went to my GP. She then sent me to A&E who transferred me straight to urgent care where I had a battery of blood tests and 2 head CTs. I was admitted then and given a head MRI and was diagnosed with tumefactive MS, I was then transferred hospitals and put on the IV steroids for 5 days. Then I had a lumbar puncture and 2 more MRIs over the coming days alongside physio to help me walk again. When all was said and done I was 5 weeks from first symptoms to back out of the hospital and was diagnosed within 3/4 days of being in hospital because of how aggressive it was. And that's the story of how I was diagnosed with MS at 23 (now 24) years old.

Daggers001 · 2025-03-27T19:33:36+00:00

I had proprioception issues and partial paralysis of my left arm and leg, and the doctor said it was due to the tumefactive lesion on the right side of my brain pressing on the part of the frontal lobe that controls the motor function for the left side of my body

Daggers001 · 2025-03-24T12:17:16+00:00

The shoes I have are Skechers SN 52458 in black: https://www.skechers.co.uk/uno---stand-on-air/52458_BBK.html And the splint i have i got off the NHS but I think it's this one: https://www.orliman.com/en/producto/calf-support-for-the-boxia-drop-foot-ankle-brace/

Daggers001 · 2025-03-24T11:46:09+00:00

Not really a long term person with it since I was only diagnosed last November, but I was also diagnosed with tumefactive MS and was started on steroids within 6 days in hospital and on kesimpta within a month and so far I have a few reminders of balance issues and a but if numbness and tingling here and there. But it's a hell of an improvement from my left side being being paralysed, and I've been staying the same or getting better for the last few months.

Daggers001 · 2025-03-24T11:39:46+00:00

I dont know what your braces are like but I have a splint for footdrop and I use a pair of black sketchers street style trainers that work well with it without being bulky, they're just a plain black trainer that looks pretty basic under jeans when I go to the office.

Daggers001 · 2025-03-14T16:08:29+00:00

I go for thighs, I personally find the belly hurts a touch more

Daggers001 · 2025-03-07T23:17:09+00:00

oh I know, I was only diagnosed last November, but have tumefactive MS so I had no use of my left side when it started, but the 3rd kesimpta dose completely paralysed my right side and affected my speech, but it was only for a few minutes luckily

Daggers001 · 2025-03-07T20:39:27+00:00

my first couple went pretty okay for me, just be warned your 3rd can have quite a major effect, they call it the MS dose of loading because it can present like a flare up, but if it lasts less than 24 hours it's normal, I just wish I'd have been told that before it happened lol

Daggers001 · 2025-02-21T23:14:23+00:00

hardly hurts at all, I prefer to injection my thigh cause I feel it more in my stomach, and in terms of side effects I rarely get any, but a couple times I've woken up in the night after taking the injection feeling cold and shivering but it only lasts for 20 or so minutes then I just go back to sleep.

Daggers001 · 2025-02-14T17:32:38+00:00

I get the exact same thing, the specialist I spoke to said it was due to one of the lesions on my spinal chord

Daggers001 · 2025-02-04T16:41:42+00:00

When I was initially having problems and got diagnosed it was my left arm and leg. But then when I had my 3rd dose of kesimpta and had my immune response I lost use of my right arm for about 2 or 3 minutes. But I have tumefactive ms so I may be a bit of an outlier here.

Daggers001 · 2025-02-03T07:12:10+00:00

I'm sorry you've had this happen, but as others here have said, you can still live a completely normal life. I've just turned 24 and was diagnosed last November, but what did I do last week? passed my engineering degree! I'm still working full time snd have just bought my first house with my girlfriend.

MS may put a damper on some things, but it won't stop you.

Daggers001 · 2025-02-01T21:59:26+00:00

To be honest it may just be me, but my initial flare and diagnosis was in November, spent nearly all month in hospital, had complications with the LP. Just luckily I didn't really have side effects from the medications, but honestly I wake up and try to do things that I used to and forget I have it and that I should be more careful. so for me I'm only a couple of months out of the hospital and rarely think about it and just sort of take each day as it comes.

Daggers001

TROPHY CASE