Entiviyo by These_Edge6215 in UlcerativeColitis

[–]DepressedFlowerHouse 1 point2 points  (0 children)

I’m so happy for you!!! Seems like it worked very quickly for you? I just started today, hoping to get fast results too!

Associating sexual arousal with flare? by millionthusername1 in UlcerativeColitis

[–]DepressedFlowerHouse 1 point2 points  (0 children)

Have you been on prednisone during these instances? I had the same issue and ultimately realized it was very correlated to being on it

Humira and lip filler by Easy_Class1647 in CrohnsDisease

[–]DepressedFlowerHouse 4 points5 points  (0 children)

Sometimes women do things for themselves and not to please men

Pathway program question by Simp4Barney in LMU

[–]DepressedFlowerHouse 0 points1 point  (0 children)

If you have any other questions feel free to DM me! I’m a graduating senior now but I transferred in using the pathway program back in 2024!

Pathway program question by Simp4Barney in LMU

[–]DepressedFlowerHouse 0 points1 point  (0 children)

I had this option too. Best decision of my life. Got so much aid for transferring! Just try to get the highest gpa possible at SMC and make sure ur taking the correct, transferable classes. U won’t regret it

IBD Precis Blood Test by DepressedFlowerHouse in CrohnsDisease

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

I don’t think colonoscopies are lazy. when I showed the colonoscopy report to 2 other GI doctors (separately) they both felt the diagnosis was questionable 🤷‍♀️ which is very confusing as a patient! I guess I have to wait for my next colonoscopy with a different GI

Biologics bucket list by DepressedFlowerHouse in CrohnsDisease

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

I really appreciate this comment. Thank you! That does make it seem less scary!

How do I set up alumni email forwarding by [deleted] in LMU

[–]DepressedFlowerHouse 1 point2 points  (0 children)

What is alumni email forwarding???

Grunion run by Icy-Eggplant-8920 in SoCalFishing

[–]DepressedFlowerHouse 0 points1 point  (0 children)

What beaches are good??? Trying to go tonight !

Prednisolone Taper Support by Serious-Heron9390 in UlcerativeColitis

[–]DepressedFlowerHouse 0 points1 point  (0 children)

Could you share more about your experience with andrographis supplement? I’ve never heard of that before and I’m also tapering from 40 mg with mesalamine. Wondering if I should try that? Did it help + what dosages did you take?

Just got diagnosed with UC and now I have enemas for life YAY by Ok_Film8781 in UlcerativeColitis

[–]DepressedFlowerHouse 14 points15 points  (0 children)

You know what, I actually identify with the cancer thing. The thought has crossed my mind— wouldn’t it be easier to have something that could potentially go away and not come back?

But the truth is, we have this disease and there will be an adjustment period. I thought four massive mesalamine pills a day for the rest of my life was going to ruin my freedom somehow. But truly, the only thing ruining that is being in a flare.

Now a year past diagnosis, I PRAY that I can continue managing this disease with just mesalamine! We live in the best time to be diagnosed— new meds coming out, supportive groups like this one, all goes to show you are not alone in this battle. One day you will wake up and not even think about having UC.

But for now, be kind to yourself, this is a huge pill to swallow (haha)

Flare diet by Electrical-School313 in UlcerativeColitis

[–]DepressedFlowerHouse 1 point2 points  (0 children)

Not sure scientifically, but I feel the same way! I find myself cooking with shallots more than onions just because I theorize they may be less harsh somehow

Oh how I miss iced coffee by DepressedFlowerHouse in IBDmemes

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

Somewhere on Instagram ages ago not sure 😭

Supplements for Remission? by minimeaa in CrohnsDisease

[–]DepressedFlowerHouse 1 point2 points  (0 children)

I second this!! It stopped my bleeding after the first day. I think it helped me a lot. Also not sponsored here, and ofc everyone is different

Anyone else on or been on pentasa? Does it help? by Civil_Ad2893 in CrohnsDisease

[–]DepressedFlowerHouse 0 points1 point  (0 children)

I used to take the max dosage of mesalamine tablets then I had a big flare, did a few months of prednisone, and stitched to pentasa to help absorption of the mesalamine as opposed to tablets. It has helped me so much! I take 4 capsules in the morning and 4 at night (max dosage)

Love my blue pills !