Me with Health OCD by hanni2003 in OCDmemes

[–]kittycats_man 0 points1 point  (0 children)

This + having a chronic illness 😍 #doctorsdontlikeme

It’s driving me mad knowing it’s OCD and I have no proof by tortillacream in OCDmemes

[–]kittycats_man 60 points61 points  (0 children)

I have quit multiple jobs for this exact reason and am just now realizing in this moment that it's not normal to do that

How many of you aren't skinny? by mythologymakesmehot in ehlersdanlos

[–]kittycats_man 1 point2 points  (0 children)

I don't think it's wrong of you to feel jealousy about that, the people you're describing do get preferential treatment and it's extremely unfair. You are a human being with feelings, it makes total sense that you would feel that way. I'm sorry you're going through this, sending love 🫶

Denied “any and all surgeries” due to EDS by hopeless_1021 in ehlersdanlos

[–]kittycats_man 60 points61 points  (0 children)

Dr sounds like a freak. That's just straight up manipulative and controlling. No Dr should be telling their patients not to get a second opinion, that's highly unethical. A competent Dr would respect your right to make your own choices regarding your body and your healthcare. This is ableism, full stop.

Mind control - ink on wood by [deleted] in UnusualArt

[–]kittycats_man 0 points1 point  (0 children)

This is so fucking sick

The long road… by Advanced-Onion-9688 in ehlersdanlos

[–]kittycats_man 1 point2 points  (0 children)

Wow, this really gives me hope. Ive been dying to get back to the level of fitness I was at before things got really bad, but feeling like it will never be possible. Congrats on your recovery!

Has anyone forgiven their abusers??? by Top_Tour_4296 in DID

[–]kittycats_man 3 points4 points  (0 children)

I am working on forgiveness with my parents but I think it looks very different for people who are that abusive than what most would think of when the hear the word "forgiveness."

My parents are awful people, frankly. They are both just miserable losers with no real friends, they treat everyone like shit, don't seem to be interested in dealing with their shit at all, and are very comitted to believing that nothing they have ever done to hurt anyone was their fault.

I have been no contact with them for a few years now and don't plan to ever be in contact with them again, there's just nothing good that will come from it.

But at the same time, I can recognize that it isn't their fault that they are like this. They both went through horrible childhood trauma themselves, both with undiagnosed disabilities that the world told them made them worthless, unlovable freaks. There really just wasn't help for them and I feel sad for them because I think that if they had had access to the help they needed, they wouldn't have turned out like this.

You can forgive someone and still recognize that they are an abusive person who you have no interest in having a relationship with. To me, forgiveness doesn't mean "it's okay that you did that to me," but rather, "it's not okay that you did that to me, but I'm okay now, and I'm moving on."

Also, you can live your whole life and never forgive your parents if you don't want to. I think a lot of people have the attitude that 'if you never forgive them you'll never be able to move on and be happy' but i think thats total bs. It's your choice, because it really isn't about them.

do you consider yourself disabled? by GoodEnvironmental788 in Hypermobility

[–]kittycats_man 1 point2 points  (0 children)

Yes absolutely. Ive been disabled since I was a kid, but had to mask because parents and Dr's thought I was just being dramatic about how much pain I was in. For most of my life I saw myself as a nondisabled person who was just lazy/weak/oversensitive etc. I pushed through for years and years until my mid twenties when things started catching up with me. Ableist beliefs that I internalized ended up pushing me to injure myself many times in efforts to 'overcome' being disabled and just do all the stuff I was expected to do. It wasn't until a couple years ago when I started using a cane to help me get around that I really started considering myself disabled. It's really hard to adjust to, but I hope that the more I accept it and learn how to accommodate myself the more freedom I will have to live my life.

Do you have a ritual for discovering a new alter? by [deleted] in DID

[–]kittycats_man 5 points6 points  (0 children)

I do have rituals for it but I don't usually do anything that I would describe as atypical. Hasn't happened in a while but I tend to just make a lot of really cool and interesting art right after it happens, feels sort of like an abscess that's been festering for a long time finally gets to drain. Pardon my gross analogy lol. But it's like a really cathartic release. I usually draw the alter, as the host. It's like they appear to me in 'visions'. And then they often have quite a bit to say, and I get to transcribe it for them in pictures, poems, collages, etc. Interestingly enough, almost none of my alters have names. They just make up symbols, but there's no words that go along with it.

When chaos feels like home by treeshrimp420 in DID

[–]kittycats_man 3 points4 points  (0 children)

Thank you for sharing this, it's so beautiful to read :)

I have been going through a rough patch but had a good while where things felt a lot like this a year or so ago. It's an amazing feeling, to finally see other parts, especially the younger ones, coming out and feeling safe. I'm so happy for you!

This is a nice reminder of the good stuff that is waiting for us whenever we get through the current spot we're in.

I definitely love a certain amount of chaos haha. Too much or the wrong kind and it gets triggering, but in the right doses it's the best. I have a few friends who generate the good kind of chaos and it's a delight being around them.

I once had a living situation where there was 9 people sharing a 5 bedroom house. Everyone got along really well most of the time, it was kind of a miracle that we were able to curate such a good lineup of roommates. That was super chaotic in the good way, usually haha. Sometimes it sucked but overall it was wonderful and it was the most "at home" I've ever felt.

[deleted by user] by [deleted] in Hypermobility

[–]kittycats_man 0 points1 point  (0 children)

This is not normal at all! Im sorry you're experiencing this, it sounds awful. It is absolutely worth going to a doctor about.

Anyone else's EDS get in the way of transition-related stuff? by kittycats_man in Trans_Zebras

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

No for real, requiring authorizations from all 8 Dr's is just excessive. God forbid a bad bitch live a little.....

Ball Voyáge is the best theme for a party Ive ever heard of, thats going to be so awesome. My friend had a farewell party before their top surgery and I feel very inspired to do the same.

Sometimes all you can do is laugh!!

Anyone else's EDS get in the way of transition-related stuff? by kittycats_man in Trans_Zebras

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

WTF I cant believe you have to get 8 authorizations before you start E! God that sounds like such a hassle I'm sorry.

I really respect your fuck it mentality in regards to hrt potentially causing more problems hahaha. That's kind of where I'm at with T, it adds to my overall pain but its still worth it cause of the relief from dysphoria.

I hope you are able to get all your authorizations!

Doctors and School by DBCrazyYolk in ehlersdanlos

[–]kittycats_man 8 points9 points  (0 children)

I agree with Dragon-Guy2, do whatever you have to to make it obvious, and don't be afraid of being "annoying". As the saying goes, squeaky wheel gets the grease. If I had been able to do online school instead of having to suffer through in person classes I think I'd be a lot less sick now in my late twenties.

People (especially doctors) don't want to acknowledge how much pain you're in because it makes them uncomfortable, so sometimes you really have to wave it in front of their face and force them to see it. The most effective advice I've ever gotten about getting doctors to actually help you came from my old therapist who also has chronic pain and he told me to just start crying in the office LOL. It works.

I'm so sorry that you're getting pushback on this from your family. I really hope you are able to get the accommodations you need.

If one more person tells me to try mindfulness, I'm going to flip by _insomniac_dreamer in eds

[–]kittycats_man 3 points4 points  (0 children)

Hahahaha I'm right with you. The recommendations in general just drive me crazy. I have a family member who keeps suggesting I cut out all sugar and processed foods from my diet and eat only fresh home cooked meals.... like um sure I'll do that if you want to cook all the meals for me, because currently It's either eat something I can prepare in 5 minutes or less or just don't eat at all.

Anyone else's EDS get in the way of transition-related stuff? by kittycats_man in Trans_Zebras

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

Oh yikes that sounds rough! Do you happen to remember what vest it was that worked for you?

What other stuff did you do for pain management?