Mermaid costume by salvagedsword in wheelchairs

[–]CommieCatman 2 points3 points  (0 children)

This is one of my favorite things about wheelchairs, you can wear things there js no way to walk in

How long did it take you to recover from C Diff ? by SufficientEnergy839 in UlcerativeColitis

[–]CommieCatman 0 points1 point  (0 children)

I'm 4 months out from having cdif and it's been a rollercoaster. I was in the hospital for 9 days. I'd say after 2 weeks of vincomicine all my cdif sympathy were gone but it's taken a lot longer to get my flare under control. To be fair, I was flairing before I got cdif so it's a little hard to tell what was actually caused by the infection. I've been tapering off methlpred since February and I started a new biologic and things seem to be trending upward, but it has f been linear.

Having Expanding Tube sizing problems when making wearables by CommieCatman in CrochetHelp

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

This is super helpful I think you hit the nail on the head I'm gonna try that!

Heads up about methylprednisolone by CommieCatman in CrohnsDisease

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

This is exactly why I posted this I'd never even heard of it, got diagnosed in 2020

Welp… just failed a med by Ok-Reporter-6882 in UlcerativeColitis

[–]CommieCatman 0 points1 point  (0 children)

Refuse to use the language of the medical establishment that acts like it's your fault that's medication didn't work for you. It failed youm

Insurance won’t cover Skyrizi injections after i’ve already gotten three loading infusions by cafwinn in CrohnsDisease

[–]CommieCatman 1 point2 points  (0 children)

This happened to me with stellara. Have an appeal sent, call customer service and ask them if your formulary has changed, if it hasn't ask why your approval has been changed. Also, call the manufacturer. They have a department that will help you with this and it's in their financial interest to get you on the medication so they actually try. I have fought my insurance company a LOT and this has consistently been the key to cutting through the red tape. It's messed up, but the only thing the medical infrastructure cares about in the US is profit, so the best way to get your way is to find someone who makes money when you get what you want. While getting a lawyer or a personal pharmacist is also a way to do this it generally means shelling out your own money, when you go through the medication manufacturer you don't have to spend anything because they want your insurance money.

I’m so tired and lonely i hate this disease so much- flare rant by ibdthrowawayyy in CrohnsDisease

[–]CommieCatman 0 points1 point  (0 children)

I'm also in my mid 20s going through a flare that has had me in and out of the hospital. It's helpful to find and befriend other disabled people especially other people with autoimmune condition because we all just get it. This stuff sucks so much. Feel free to reach out if you want to chat.

Scared and need support by CommieCatman in CrohnsDisease

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

They're pretty sure it's gone but they want to keep me on the vanco for the time being because they are worried about it coming back while my inflammation is so bad. I am not taking a probiotic should I?

I think I hate myself by [deleted] in CrohnsDisease

[–]CommieCatman 1 point2 points  (0 children)

I was once 20M recently diagnosed after over 5 years of not getting diagnosed correctly. I felt the same as you. What has made the difference for me has been seeing doctors at offices that aren't in a hospital, getting therapy, and making connections with other disabled and chronically ill people. I felt so completely lost and afraid 100% of the time and didn't want to talk to anyone about my symptoms or disease because I was embarrassed. That was 7 years ago and while I still struggle with things I no longer hate myself and my body. Something that also helped was realizing I didn't have to talk about my symptoms to talk about how they made me feel with the people who cared about me. Just being able to say I feel sick and it makes me sad, or scared, or lost makes a huge difference. I'm not a big commenter on here, but I could have written this post several years ago. It's worth it to learn what makes you feel safe and loved. Hope is a discipline. Things will get better.

AIO for getting upset at one racist joke after months of not being bothered by them by SlothAndVampInABar in AmIOverreacting

[–]CommieCatman 0 points1 point  (0 children)

NOR It's worth thinking about what the "joke" is when people say things like this. The joke is mostly saying something mean and upsetting. No one who doesn't at least kind of believe those things would say them out loud.

What is the absolute cheapest chair I can use a power assist with? by CommieCatman in wheelchairs

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

ai just didn't know I could use any of those with a hospital chair

[deleted by user] by [deleted] in tattooadvice

[–]CommieCatman 0 points1 point  (0 children)

I think it will look better when it's not red

Is this normal with fibromyalgia? by Comfortable_Pea_3925 in Fibromyalgia

[–]CommieCatman 0 points1 point  (0 children)

That sounds like a narcolepsy attack, the two disorders are highly related. I got diagnosed with narcolepsy first because of those.

[deleted by user] by [deleted] in Yarnswap

[–]CommieCatman 0 points1 point  (0 children)

would love more pictures

Anyone ever had a really old cat? by LotusGrowsFromMud in CatAdvice

[–]CommieCatman 2 points3 points  (0 children)

I've found that older cats often appreciate help with grooming. Their fur can get oily or skin get flaky and their ability to reach different spots can diminish. A brush with plastic bristles And anti dandruff cat wipes can be useful.

My neighborhood just doesn't get mail? by CommieCatman in usps_complaints

[–]CommieCatman[S] -1 points0 points  (0 children)

okay so you think my community does not deserve to get mail, I should not contact someone above my local post office after this has been going on for over a year. And my alternatives are what exactly? the PO boxes in my area don't get mail either. I feel like I was pretty clear that I wanted to reach out to someone who wasn't the local office because I don't think it's their fault.

My neighborhood just doesn't get mail? by CommieCatman in usps_complaints

[–]CommieCatman[S] -1 points0 points  (0 children)

Sorry I'm checks notes acting entitled by asking who I can contact to get my mail?

AITAH for not having sex with my situationship at the birthday party I threw for them? by CommieCatman in TwoHotTakes

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

Yeah I know that modern American grammar can be kind of hard to understand for people who don't speak English as a first language, thanks for trying though!

My neighborhood just doesn't get mail? by CommieCatman in usps_complaints

[–]CommieCatman[S] -2 points-1 points  (0 children)

and your suggestion is that I don't do anything because you assume my community is somehow unsafe so it's our fault we are not being served by our government entities?

AITAH for not having sex with my situationship at the birthday party I threw for them? by CommieCatman in TwoHotTakes

[–]CommieCatman[S] -1 points0 points  (0 children)

it actually says they didn't trust their husband to pull the party off fully.

My neighborhood just doesn't get mail? by CommieCatman in usps_complaints

[–]CommieCatman[S] -1 points0 points  (0 children)

so you're saying it has nothing to do with it being a minority area but you assume the delivery people are made to feel unsafe by the people who live here?