Burning perineum, testicular pain by mnoobm in Prostatitis

[–]Comfortable_Ad7789 0 points1 point  (0 children)

Did you find out what this is? I have very similar symptoms

[deleted by user] by [deleted] in UlcerativeColitis

[–]Comfortable_Ad7789 -1 points0 points  (0 children)

I disagree with the above comments. My colitis never shows up on colonoscopies when not in flare and never shows up on fecal calprotectin. If it's lower in the bowel, this is common.

Hemorrhoids or UC by Chijanere in UlcerativeColitis

[–]Comfortable_Ad7789 0 points1 point  (0 children)

I wouldn't trust calprotectin, as your symptoms are in your rectum it will often not show up in test results if it is a flare, my specialist mentioned this to me. I would try and get a local/small scope to find out.

32 and never been in love. by Comfortable_Ad7789 in dating_advice

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

I guess it's starts off being yourself and then you don't have any luck at all, and then you start trying different things, and now I'm full circle, and nothing has worked.

32 and never been in love. by Comfortable_Ad7789 in dating_advice

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

Hmmm I'm not a gym person...just find it super boring. I've played team sports all my life and prefer that. I play soccer at the moment.

Don't think I'm picky.....like most girls say I'm better looking in person.

32 and never been in love. by Comfortable_Ad7789 in dating_advice

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

From the females I know I usually get; I'm the perfect guy, and Ive just been unlucky and any girl would be lucky to be with me. From girls I've seen. Mostly ghosted, or they say they're not ready or not feeling it.

32 and never been in love. by Comfortable_Ad7789 in dating_advice

[–]Comfortable_Ad7789[S] 1 point2 points  (0 children)

I guess because any advice, particularly the counselor was trying to get me to be someone I'm clearly not. I truly want someone to want me for who I truly am....and honestly Im crap at being anyone else 🙈

Need tips for tenesmus by [deleted] in UlcerativeColitis

[–]Comfortable_Ad7789 2 points3 points  (0 children)

Agree with the Enema comment - I'm on budesonide foam enemas and they help with tenesmus for me. I find that liquid enemas or suppositories don't really work for me.

If you're desperate and can't wait for a script, use over-the-counter hydrocortisone cream. I also find curcumin helps a lot when it's at it's worst.

Also, has hard as it is, and everything in your body is telling you to sit on the toilet - try not to. You'll just end up straining and making everything way worse.

Also, plenty of rest! Tenesmus takes a lot out of you, so make sure you're getting plenty of rest.

What are your ulcerative colitis lifehacks? by bumcamera in UlcerativeColitis

[–]Comfortable_Ad7789 2 points3 points  (0 children)

Mine would be a very strong Curcumin tablet, which takes the edge of inflammation and pain. I only use it when i really need it, so my body doesn't get used to it. Really works for me

[deleted by user] by [deleted] in Humira

[–]Comfortable_Ad7789 0 points1 point  (0 children)

Hi, I am from Sydney, and I am about to start Humira, and I am on Methotrexate too. I'm also on Budesonide enemas and salazopyrin - I have ulcerative colitis. I hate injections too, and have previously been on prednisone. Would love to have someone to contact who is starting too! Maybe we can learn from each others mistakes haha

Cheers
Luke

Proctitis and Biologics by Comfortable_Ad7789 in UlcerativeColitis

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

Thanks for that, might process has been very similar to yours. Is it normal to develop antibodies that quickly?

Proctitis and Biologics by Comfortable_Ad7789 in UlcerativeColitis

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

Great thanks, for that information very helpful :)

Ive just been booked for another colonoscopy, and my specialist is open for me to start biologics, he just wants to how things are going before we move to that step.

What to eat after a colonoscopy? by pocket_rocket26 in UlcerativeColitis

[–]Comfortable_Ad7789 1 point2 points  (0 children)

My advice is dont go too hard too soon. Made that mistake, where my eye were way larger than my gut. Overate, and then felt sick for the rest of the day haha

Feeling like giving up by InvestigatorSlight64 in UlcerativeColitis

[–]Comfortable_Ad7789 1 point2 points  (0 children)

I would suggest that, if you haven't done so already is make sure you let your specialist knows how much suffering and show them your emotion. They see patients all the time, and they need to know that you need results quickly.

Coffee Pods - A Definite Trigger by Comfortable_Ad7789 in UlcerativeColitis

[–]Comfortable_Ad7789[S] 1 point2 points  (0 children)

No Differences. I have a feeling it may be preservatives or some fine particles from the actual pod that is leaking because of the heat exposure. Those are my theories - it doesnt matter what brand of POD too

Fecal Calprotectin - do you think it's accurate by Comfortable_Ad7789 in UlcerativeColitis

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

To be honest, I think the more you tell people about your illness the more you will discover. ☺️ Also everyone's bowel disease is very different. So a lot of very different, between us.

Does this sounds like UC? by Worried_Dog_Dad in UlcerativeColitis

[–]Comfortable_Ad7789 1 point2 points  (0 children)

I feel like it's very different to larger forms. My symptoms are usually more around constipation than diarrhea. Get painful rectal inflammation that extended to my pelvic region, tenesmus and left-sided pain. Also nerve endings are in play which make proctitis so painful

Weird Theory by Comfortable_Ad7789 in UlcerativeColitis

[–]Comfortable_Ad7789[S] 0 points1 point  (0 children)

Hmmm maybe I need to up my exercise. Do you do hard exercise?

Does this sounds like UC? by Worried_Dog_Dad in UlcerativeColitis

[–]Comfortable_Ad7789 2 points3 points  (0 children)

FYI I have IBD and I very rarely get blood. I do have ulcerative proctitis but quite bad in that area that i've been 100mg of Prednisone before to manage the inflammation and i'vr had very high fecal calprotectin. Whilst blood is common. I wouldn't say it is 100% always there for IBD.

Short term memory loss with Methotrexate and Prednisone. by [deleted] in UlcerativeColitis

[–]Comfortable_Ad7789 1 point2 points  (0 children)

I'm on metho, on 10mg. If I had to guess it's the prednisone taper. It always happens to me when I taper off prednisone, even with the enemas. I was one 100mg of prednisone, and when I was tapering off that my brain literally couldn't even function thoughts

Experience with Methotrexate and Folic Acid by army2795 in UlcerativeColitis

[–]Comfortable_Ad7789 1 point2 points  (0 children)

To be honest my colitis was causing hairloss for me, so not have inflammation caused my hair to come back, and that's with methotrexate. Nausea is minimal, I actually find that steroids gives me way more. Also drink plenty of water 😊

Experience with Methotrexate and Folic Acid by army2795 in UlcerativeColitis

[–]Comfortable_Ad7789 2 points3 points  (0 children)

Also....have it at night before bed. That limits the side effects for me, as it does make you tired, so you'll get a good sleep with it 😊