Angry Guts Profile picture
Oct 23, 2018 9 tweets 4 min read Read on X
I don’t know what I would do if I didn’t find a whole online community of #JPouch-ers.

Every time I look up some symptom to see if it’s related to my pouch, I find hundreds of others with the same problem, related to their pouch.

And it’s all things doctors never told me. 1/
The thing with a #JPouch is, for those with colitis, it’s seen as a cure. No colon, no problem. They warn you that you can likely develop Crohns later on. They tell you about the occasional inflammatory pouchitis. 2/
CN ////// menstruation, fertility
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But what about severe period cramps and extra digestive trouble during your cycle? What about lower back pain radiating from your pouch or as a result of surgery? What about difficulty conceiving due to internal surgery scars? 3/
Each poucher experience is unique of course, and there’s no way to prepare everyone individually for what their pouch journey will be like. However, there’s enough of these things that I’ve seen amongst SUCH a large group of people that I think they’re worth talking about. 4/
Like, from the get go.

All doctors are different too. But when I got my #JPouch, it was presented to me as something to “give me my life back.” My surgeries were all planned with a #JPouch in mind, and I really wasn’t given much information on it. 5/
It was a medical choice basically being made for me because it would be the most “normal.”

And I’m thankful for my #JPouch (most days) because I handle it better (again, most days) than I did my ileostomy.

But there is still pain. There are still overwhelming difficulties. 6/
I face new obstacles regularly because of my #JPouch. New pains, new problems, and the only people who can give me any insight are the thousands of folx online sharing their experiences.

I’m thankful. But I still feel like things about this procedure were swept under the rug. 7/
In conclusion, I really just would like to see:

-More doctors being more honest and open with their patients about the possible long term effects of their surgeries.
-More research done on common #JPouch issues and more solutions.
-The online #JPouch community continuing to- 8/
-support each other, because we are the ones who know our conditions best and we get each other through hard times.

Someday I’ll do a follow up thread of my own symptoms and co-morbidities to discuss, but for now, think about this.

9/9

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More from @ShutUpDanni

Sep 25, 2020
As we battle the ever present “what about personal responsibility?!” healthcare argument, I’m here to tell you: it doesn’t matter.

I’m disabled. I didn’t become that way by my own hand - it was entirely an accident, and I was a child doing child things. But here’s the thing: 1/7
That does not make me more worthy of accessible care.

Whether an illness or injury was caused by genetics, accidents, heroism, alcoholism, drug abuse, poor eating habits, lack of exercise, it literally does not matter.

Human beings deserve to get care when they are ill. 2/7
EVERYONE deserves care when they are ill, and I do not care if they are someone working 80 hours a week to make ends-meet, someone living under the poverty line on disability benefits, or rich enough to take care of it even at its current ridiculous price - EVERYONE. 3/7
Read 7 tweets
Jul 11, 2020
Okay, I’m gonna give a quick story time.
I feel that some of you are still operating under the pretense that “I’ll probably survive COVID, so I don’t have to worry.”
You do.
Because the fact that fully healthy, abled, young individuals have died as well aside, you are 1/7
forgetting the fact that illnesses don’t leave without leaving things behind.

I know this firsthand.

I had pertussis 8 years ago, when I was 18. My immune system was very poor at the time (and remains so).

Prior to getting pertussis, my lungs were VERY strong. 2/7
I was a choir student from when I began school until I finished. A soprano who trained and competed whose preference was opera. I was also in a band and sang acoustic pop punk covers, almost every weekend. I had also been an avid swimmer most of my life. Once the weather 3/7
Read 7 tweets
May 4, 2020
Friends, propaganda has sprung to using misleading statistics as per usual, so as an ex-sales associate, let me put it in perspective for you.

My mother in law’s conservative radio show is trying to downplay COVID by stating that the death rate in NYC is ONLY .01% 1/4
Sounds small, right?

NYC has a population of 8,398,748 people.

.01% of that number?

About 840.

That is 840 people, dead. 840 people with families, friends, memories, dreams, futures that were torn from them.

If you hear statistical propaganda, please do the math. 2/4
It’s a common trick to try to present percentages in a dismissive fashion because it seems smaller.

In sales, we’re taught to talk in money, because $100 off $1000 sounds a lot sweeter than 10%.

Don’t be fooled - these numbers are NOT small.

And even if they were? 3/4
Read 4 tweets
Apr 20, 2020
CN //// drugs
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I live in an area that is pretty much a heroin hot spot. We’ve had 4 (if not more since I last saw reported) overdose deaths during this time. And every single comment from locals on the matter has been nothing short of heartless. 1/6
As a disabled person, I’m not new to the cruelty of human beings. I know exactly how shitty people can and will be to each other in any given circumstance. But this is just too obscene for me to deal with. This is HARD. Quarantine, COVID, this situation is hard for EVERYONE. 2/6
Imagine how hard it is for those who were already battling such terrible demons. Imagine losing your support lines and being forced to be alone with nothing but your pained mind. This is one of the worst things that could’ve happened to those in recovery 3/6
Read 6 tweets
Jan 21, 2020
From reading @coffeespoonie’s saga on the inaccessibility of Uber drivers refusing to follow the law, one of the hottest takes I’ve seen so far is “you should have to identify yourself as disabled before using any service.”

No. We are not doing this. Here’s why. 1/6
Abled people enjoy ignorant bliss in the form of “nobody would willingly discriminate against disabled people”, but it happens. Every. Single. Day. This is our lives. Why would you suggest that disabled people sign themselves up to be discriminated against ahead of time? 2/6
This is why:

Whether it’s conscious or subconscious, you do not see disabled people as people. You would rather we not exist in society with other people. You’re “fine with us being disabled” (as though we had a choice) but you want that kept far away from you. 3/6
Read 6 tweets
Oct 3, 2019
CN // Medical Abuse

Just read an extremely disturbing and triggering article about hospital staff creating a miniature “Wall of Shame” based on patients CONFIDENTIAL MEDICAL RECORDS, making fun of disabilities that they found funny for some reason. 1/5
This was triggering because I have an “embarrassing” disability. I’m one of those people. And I already have an extreme aversion to hospitals and medical facilities (to the point where I have almost died because I refused to go in for care due to such extreme anxiety). 2/5
To read something like that reminds me how little people think of disabled people, like me. Reminds me that no matter where I go, I will always be mocked, even by those I am entrusting my care to. People who do not have to wake up every day facing the hell that I face. 3/5
Read 5 tweets

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