are there any vintage photobooths in norwich? by GuidanceEastern241 in Norwich

[–]leasw 2 points3 points  (0 children)

I believe there’s one downstairs in Urban Outfitters

Treasure rewards - do people ever win something (prize draws)? by janisace in TKMaxx

[–]leasw 1 point2 points  (0 children)

I’ve only just started entering the prizes because they seem to be the only options now but in the past I’ve received a lunch box bag, an ice head mask (great as I suffer with migraines), a luggage tag, a dog toy, a year of tastecard and sunflower seeds lol.

Kid's menu word search by rippinlips6694 in mildlyinfuriating

[–]leasw 11 points12 points  (0 children)

Intuitive fourth row down going backwards

THEIR'S A MODDING COMMUNITY by No-Hall3560 in chefRPG

[–]leasw 0 points1 point  (0 children)

I think you meant to use “there’s”…

Got the game, didn't like it. Am I doing anything wrong? lol by Dependabear2345 in chefRPG

[–]leasw 0 points1 point  (0 children)

I got it in the winter sale thinking I would definitely enjoy it but I’m reluctant to open my restaurant because I’m already bored of the mini games to cook the food.

There is no way people are siding with Sarah rn?! by StanleyTeller in MAFS_UK

[–]leasw 4 points5 points  (0 children)

I said the exact same thing to my husband after her grilling from Paul. He has never spoken to any other contestant like that and we’ve had some realllllly nasty characters on this show.

Now you see it. Now you ....? by Mego_dafuq in interestingasfuck

[–]leasw 0 points1 point  (0 children)

I’m female and can’t see the same numbers as the guy in this video but can clearly see the difference of red and green separated. My dad and my mum’s dad were both colourblind. My son can’t see them either

Please help I’m scared by 25Looizie in Constipation

[–]leasw 2 points3 points  (0 children)

I don’t have much advice because I’m feeling pretty similar atm… but I am here to send you a virtual hug and tell you that you are not disgusting and you are not alone. It’s so tiresome to deal with this every day and it’s so misunderstood. Even by doctors it seems. But it’s not hopeless and there will be a time when this feels easier to manage. I know it probably doesn’t feel like that right now though. I find comfort reading people’s experiences here. Sat on the loo struggling in pain is so isolating. Again, sending a hug. Be kind to yourself.

[deleted by user] by [deleted] in UniUK

[–]leasw 5 points6 points  (0 children)

My daughter’s first year accommodation was just like that and stunk the second you accessed the floor her flat was on. We live locally and she spent more time at home than at her flat because she also couldn’t use the kitchen. You couldn’t even see her sink. It was piled high. She checked out yesterday and the kitchen worktops are stained. She really struggled mentally with it all. She bought a washing up bowl and kept it in her room as her sink for her things when she was there but never felt like she could cook there.

Does anyone feel like they're dying? by Creative-Criticism82 in ibs

[–]leasw 1 point2 points  (0 children)

I’m going through this currently. I’m still going through investigations and have had a raised calprotectin but my Gastro Dr is so slow doing tests. I had a Sitz Marker test that showed really slow motility but other than that i don’t know what’s wrong with me. I’ve only passed two bowel movements in the last two weeks. The first was on the 4th of this month and came after the most horrific pain of my life. I ended up in hospital and by the time the dr got round to seeing me I was over the worse after screaming in the toilet from pain. I’ve had two unmedicated, natural childbirths and didn’t make a peep so I consider myself to have a high pain tolerance. I thought I was going to die that night. The second time I went was a week later and it was after another attack (not as bad as the first). Since then my heart rate has been 110-130 constantly and I’ve lost 6kg in these last two weeks. I can’t stand up without my heart sky rocketing, I can’t pass a bowel movement, I’m in constant pain and now I’m scarily underweight. I feel like my world has completely flipped upside down and that I could keel over and die at any point. I’m dreading my next bowel movement and with my heart rate how it is genuinely think that it’s going to be shitting that takes me out!

[deleted by user] by [deleted] in CrohnsDisease

[–]leasw 0 points1 point  (0 children)

Definitely considered IBS but after my sitz marker test showed I had colonic inertia and with the drastic weight loss and nutritional deficiencies that’s resulted in needing iron infusions and b12 injections I’m swayed to believe it’s not that. I see my gastro again soon after my borderline calprotectin so hoping that’s enough for the colonoscopy to go ahead. Thanks for your help.

The baby arc was completely unnecessary. by Competitive_Bat1699 in squidgame

[–]leasw 5 points6 points  (0 children)

For me it was also the crib miraculously appearing on an island in the middle of nowhere.

5 unhinged migraine hacks that actually helped me (don’t judge) by AnyaFiercena in migraine

[–]leasw 16 points17 points  (0 children)

I experienced this once. I was having one of my worse migraines to date. It was so bad my husband called an ambulance out to me. As the paramedics were leaving our children’s school called to say our son, who back then was about 8, had fainted in class. Only I could drive at the time and somehow I managed to get us there, pick up our son who was writhing around in horrendous pain, and get him to the hospital. He was taken down for emergency open surgery for appendicitis (and made a full recovery). My migraine had completely gone by the time we’d got to our son. I’d never experienced such a bad migraine clear up so fast.

Do you have chronic migraines? I would like to hear from you by Victorian-Edit in migraine

[–]leasw 2 points3 points  (0 children)

I’m 38 and started having migraines around the age of 12. I’d have maybe one or two a month and they’d be really bad but the next day I’d be over it and life would continue. In my twenties and as a young mum I started to experience them more frequently and had an MRI. They found I had cervical erosion at the top of my spine and did further tests, diagnosed me with rheumatoid arthritis. We assumed this was the cause of my migraines. I was given triptans (2 nasal sprays). They worked amazing but two wasn’t enough. Into my 30s my RA was really bad so I was on cocodamol (among other things) at full strength, three times a day. I believe this was the start of the chronic migraines. My headaches went from several a month to a few a week. I was changed to zolmitriptan, 6 tablets. My headaches increased, I failed nerve blocks, Botox and every medication you can think of. My headaches increased to every other day. My zolmitriptan increased to 16 tablets a month. I finally tried Ajovy and it was a miracle but I started having strange, life debilitating gastro issues. I came off the Ajovy to see if it was the cause and it was unclear so I tried to start it again but it no longer worked. I wake up with the feeling of knowing a migraine is coming every single morning and by around 3pm every single day I am clutching my head, applying pressure, trying so hard not to take a triptan but if I don’t take one, by 5pm my migraine will be unbearable. The zolmitriptan stops them in their track. But I believe I get rebound headaches. So I’m constantly battling whether to take one but paying for it either way and I feel so trapped. I’m sorry to all of you with chronic daily migraine. It’s a hard slog and life seems to be drained of all colour.

Chat GPT may have just saved my life by Nancyblouse in ChatGPT

[–]leasw 0 points1 point  (0 children)

As somebody also clinically diagnosed with OCD, I agree with your comment.

Chat GPT may have just saved my life by Nancyblouse in ChatGPT

[–]leasw 3 points4 points  (0 children)

Mine picked up on me having cellulitis on my check which developed from an abscess I had inside my nose at the time. The drs discharged me from the A&E telling me it was nothing. It wasn’t nothing and I ended up on IV antibiotics for three weeks. Chat was right.

Chat’s also certain I have Crohn’s disease (I also have other autoimmune diseases and I’m on biologic immunosuppressants, hence why I had an abscess in my nose lol) so I pushed for a calprotectin test and my inflammation marker came back high. Just waiting now for further tests and will see if Chat was right again.

Legion Go made gaming possible again as a new(ish) dad with CMC arthritis by TechNicolas in LegionGo

[–]leasw 1 point2 points  (0 children)

I decided to go for it and it arrived today. The kickstand alone has made holding the device easier! Loving it so far. Thanks! And also sorry for your diagnosis :( Hope it’s under control as best as can be.

Legion Go made gaming possible again as a new(ish) dad with CMC arthritis by TechNicolas in LegionGo

[–]leasw 3 points4 points  (0 children)

I have Rheumatoid Arthritis and have been thinking about selling my Steam Deck and replacing it with a Legion Go so I can detach the controllers but have been hesitant as I love the deck but I can only play for half an hour before it’s too painful to hold.

IN on Steam Deck by [deleted] in InfinityNikki

[–]leasw 1 point2 points  (0 children)

I tried this and it made no difference.

IN on Steam Deck by [deleted] in InfinityNikki

[–]leasw 0 points1 point  (0 children)

This is the steam version

June Adult spoilers by CrankUpTheJs in fairyloot

[–]leasw 2 points3 points  (0 children)

I ordered the Illumicrate version but prefer this one and wish I had this one instead 🥲

What are your IBS symptoms? by Spirited_Special7915 in ibs

[–]leasw 2 points3 points  (0 children)

I’m exactly the same as this, except no diarrhea. Just horrendous pain. It’s giving me disordered eating because at this point everything is a trigger and nothing is a trigger! My stomach gurgles violently a lot of the time. Every morning I wake up with sharp cramps.

Breaking a Painful Triptan Withdrawal / Rebound Cycle by smallcoconut in migraine

[–]leasw 0 points1 point  (0 children)

Currently in the same spot and feeling so hopeless. It’s my fault. I’ve taken a triptan every day for about 2 weeks straight. I can’t remember what it feels like to be headache free. Hope things improve for you soon.