This case highlights the potential role of SARS-CoV-2 in triggering lymphocytic colitis, emphasizing the need for further research and vigil
I have a friend who has microscopic colitis. She got it after being sick with a virus.
seen from Russia
seen from Brazil
seen from Malaysia
seen from China
seen from China
seen from United Kingdom
seen from United States
seen from United States
seen from United States
seen from United States
seen from United States

seen from United States
seen from China

seen from United States
seen from Poland
seen from Netherlands
seen from Türkiye
seen from United States
seen from France
seen from United States
This case highlights the potential role of SARS-CoV-2 in triggering lymphocytic colitis, emphasizing the need for further research and vigil
I have a friend who has microscopic colitis. She got it after being sick with a virus.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Take care, I hope you feel better soon!❤️
Thank you! Doing my best, it’s been over a week, still testing negative for the big C but who knows these days? I’ll just stay in my room til I stop coughing I guess. But Hopefully back on my feet soon. Here’s a little Self Care-O in the meantime
Life is garbage
Me, everyday always
Inflammatory Bowel Disease life

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
MRI & Chronic illness life
Hi everyone! I went for an MRI on my spine yesterday and my Sacroiliac joints. I must say out of all the MRIs I've ever had, this was the worst as my head was in a "cage" and I had to lie for an hour completely still. I was very uncomfortable and sore on the table too, but it is over now and nothing compared to a colonoscopy! Oddly I've started to compare everything negative in my life with a colonoscopy! I won't get the results of the scan until next month and they wouldn't let me see it. I was so excited to see my spine! So here is hoping my ankylosing spondylitis hasn't got worse. However I feel within myself it has as I'm always in a lot of pain especially in the morning. In my personal life I guess everything is going ok. I'm still living with my Dad, which has its ups and downs. I'm very much used to living on my own with the dogs and my own space and so is he. So I'm finding that very difficult. However financially it's brilliant as he can support me. Which I feel guilty about but there is nothing I can do to help now in my current financial situation. I hate what my chronic illnesses have put me through. Most other young women my age have kids, a house, a husband/wife etc. Yeah and I'm still at home living of my parents. But I'm still alive and I have that to be thankful for. This June I finish my under graduate degree in human anatomy and that has been my reason to keep fighting for many years and I'm so proud of myself for even considering continuing studying with my health. I'm only fit for one day a week and after many years I've finally got there. However, now the plan was to go on and study medicine but I know that I will never be physically fit to do that as we are taking 16 hour shifts in the hospital 5 times a week until I get established, which would be about 7 years from now. So I need to decide between a masters in my field or perhaps teaching. Either way I need to continue studying to get a job. I don't know if I will get funded or not and if I don't I will have to get a job somehow, which probably hasn't got anything to do with my career whatsoever. I find myself getting anxious over all these decisions and feeling a little lost and overwhelmed. I'm also still on the dating scene and I'm seeing a guy now who has just been amazing, but I haven't told him about my chronic Illnesses yet and I don't know how to tell him. The last guy I dated ran a mile after I told him! If I was in the other shoes I don't see how it could change my feelings or attraction to another person. It gets me down that we are judged on our illnesses. Anyway there is a wee update on me and my life. I hope everyone is doing as well as can be. Much love Crohns girl in pain Xox
so I got diagnosed with microscopic colitis a bit over a week ago and started on budenofalk/budenoside five days ago, just 3mg once a day, and every day since then I've had the most horrible headaches that hasn't been at all affected by pain killers, and have lasted all day. As an experiment today I still haven’t taken my budenofalk and the headache I woke up with was immediately vanquished by an aspirin, which sure makes it seem like that steroid is the culprit. Buuuut I really should be taking it to help my microscopic colitis, for just over 11 more weeks actually, but I can't imagine getting my day to day to function at all if my head hurts so much? Like I'm used to having headaches very often but usually pain killers will do something about them, they just haven’t in this case. Does anyone know if you start feeling the side effects less over time as your body gets used to it? I'm going to contact the hospital to clear some things up, but it would be great to have some 'real' peoples experiences, if you have any to share!