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Sad feelings for no reason

Today has been rough. It was the first day without a cigarette. I put a patch on this morning and it hasn't fallen off thank goodness. I've had some cravings for a smoke but I'm staying strong and pushing through. I'm doing much better than I expected to do.

But my mom won't talk to me today because she has my daughter until tomorrow night. Backstory, I lost custody of my child 12 years ago and live in a different state then my family. I haven't seen my mom in 6 years. I've asked her to come visit me but she refuses. She's ashamed of me for being transgender. She thinks she did something wrong to make me this way. So she still gets my daughter every weekend and won't talk to me. It's difficult but I'm kinda used to it I guess.

I messaged a few of my friends but nobody answered me. I feel very invisible and alone. I did talk to one person that I sent a birthday present to this week. I sent him 2 different teas that I enjoy and wanted to share with him. He's going to make it tonight with his dinner. I can't wait till he tries it so we can chat about how yummy it is.#Depression sucks so much. At least I don't have a migraine and my tummy is doing ok today. I got sick very early this morning but it only lasted for about a half hour. #CrohnsDisease is horrible but my meds seem to be working. I've only gotten sick 3 times in the last 3 weeks. It's definitely progress. And I only got sick because I didn't take my midnight dose of sulfasalazine. I tried to be awake for it last night but I was exhausted.I am going to try to make roasted mushrooms for dinner tonight. It's super easy and delicious and healthy. I am very low on energy so easy dinner tonight.

#CheckInWithMe #SchizoaffectiveDisorder #PTSD #tryingmybest #Smoking

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Do you mind sharing something that happened today or this week that made you happy or just something you really want to share with the world?

I didn’t have a great day and sometimes just having someone reply or ‘talk’ to me reminds me that I’m not alone in this world. #Depression #Anxiety #tryingmybest

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Let's talk about disability

I can’t remember how exactly it was phrased (and I can’t even find it now), but the other day I saw a post on Instagram about being disabled and it was something along the lines of disability is society’s fault. I am aware looking back on it now that it’s probably more focused around more visible disabilities - for example, it’s difficult to get a job if you can’t get to the interview because there isn’t a lift and you’re in a wheelchair or can’t use stairs. However, the post really annoyed me, and the reason it annoyed me was because I’d just had an exam in college that went insanely badly. That sounds really superficial until I tell you the reason it went so badly was that I didn’t get to sleep til midnight and I overdressed because it’s been really cold up here and messing with my EDS and then I’m pretty sure I had a combination of PoTS and an anxiety flare so I literally froze up and couldn’t play. I have never felt so disabled in my life and it only got worse when I got my feedback back and found out I got the lowest mark out of all the violists in college, including the person who barely practised, when I know that on a good day I’m better than at least three of them. I know 100% I’m better than that and it’s really hard to get over because although I know it doesn’t define me as a person, I got that bad grade because of my disabilities and conditions.
It’s very hard to explain this to your average healthy person because if you say “I got this grade because of my disability” they automatically assume that it is the responsibility of the person grading you. When I say this, what I really mean is “I could not perform my best because my body let me down”. The same thing applies when I get locked out of my debit card because my brain swears the PIN is x and its actually y or go to the grocery store and forget the main thing I came to the store for, every single time, or submit an awful essay awful which I would not have put in had I not been sick and too stressed out to proof read (it was a group essay and obviously we put it in the day before the deadline). In my view, when you put the blame on society for disability, especially disabilities that are complex and affect much more than the thing they are known for, you are effectively saying that the only reason people can’t do things is because society isn’t allowing them to, which belittles the impact disabilities have on our lives. If I’m having trouble functioning today, it’s not because society isn’t letting me function. Yes some elements of society can make it easier for me to function, for example those badges you can get in England asking for a seat, but ultimately it’s because my body is not working the way it should and I think it would be much easier for us to function successfully if more people understood this.
#EhlersDanlosSyndrome #PosturalOrthostaticTachycardiaSyndrome #ChronicPain #tryingmybest #uni #Anxiety

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