Unknown illness you never fail to amaze me cause wdym I had a sip of regular shmegular coffee earlier and could feel my heart HURTING. It never does that. Unknown illness why must you bother me with medical mysteries

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Unknown illness you never fail to amaze me cause wdym I had a sip of regular shmegular coffee earlier and could feel my heart HURTING. It never does that. Unknown illness why must you bother me with medical mysteries

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Some days I wake up and I feel so much excitement for the day. I am so excited to do things, to be active, and to exist. Then I am hit with the realization that I cannot do those things. I can try but I only get through one thing before I hit the wall. 6 months ago I could have done those things, but the changes have happened so quickly. I’m not sure when I’ll be able to do those things. I’m not sure if my brain will ever adjust to the urge to do so much and the inability to do so. I’m sure I’ll adapt and figure things out. I’ll ask for help and find new systems, but for now it’s just hard. This week they’re doing more tests. I wonder when it’ll be the test that’ll finally have answers?
I hate to be that person on here but I’m having such a crisis I’ve literally been crying to the point of almost throwing up and I feel the urge to do things I haven’t had the urge to do in a long time now.
I’ve been flaring up for like 2-3 weeks, and it’s been worse than ever before. My mobility is terrible, I’m getting low-grade fevers and flu-like symptoms every day. I’m in a lot of pain. My skin burns. I’m napping 2-4 hours most days.
Since I started going way downhill when school started, and I am constantly pushing myself to my energy limits to keep up, that school was the reason. I’ve been deliberating on leaving (I’m in nursing school and it’s super rigorous and long hours for me).
First crisis- I find out that if I do a medical leave of absence I’m potentially going to have to pay $10k out of pocket because they take away my grant money. I CANT WORK because I’m disabled, I just go to school. My husband provides for us and we’re trying to save money to start our life. This amount of debt out of pocket would cripple us.
Then, I go to my rheumatologist for an urgent appointment. I tell her about my symptoms. She says that my lupus and fibromyalgia are both managed really well, and my symptoms aren’t from either of them. She said she doesn’t know what’s causing my symptoms, she is concerned, and I need to see a neurologist. She didn’t think school was the cause.
She tells me that I should stay in school because I’m going to feel worse at home, even though I feel terrible afterward. She said I wouldn’t qualify for disability because my diseases don’t explain my symptoms. She said I need to do more therapy, do mindfulness and think positive.
She said it’s my choice to make about school but I can’t do *nothing* (I know that), and that I’ll feel bad and lose my self worth if I stop going. She said if I didn’t want to be a nurse that was okay (not the reason at all that I’m considering leaving but honestly at this point fuck it all).
I don’t know how to do this. I just don’t. I can’t do it anymore. I sobbed on the way home, told my mom I don’t want to talk about it, and now I’m crying in the shower.
I’m basically at square one again with what the fuck is wrong with me, have no idea what to do about school, and my will to live is so low it’s in hell. I have no idea what to do. I already missed a clinical, so I’ll have to pay to make that up and then do 2 9-hour shifts in the same week when I’m already burnt out from one.
sorry for my inactivity, i'm not doing well. i hope to be back soon ♡ feel free to comment any songs or shows for me to listen to/watch, i need the distractions :)
Love waking up feeling like I just got beat up by some chump but only on one side of my body.

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Hm question to my disabled folks who suffer chronic all over body pain and chronic heavy never goes away exhaustion. Mobility aids?
Cane's don't seem to work well for me.
So i was thinking crutches. But I'm so tired all the time that I worry that wouldn't work either.. but being plus sized. And young. I'm so scared of judgement by others over me being in a wheelchair.
But. My current thing is is i don't have a diagnosis yet. But I've been seeing doctors for almost 5 years trying to find out what is wrong. Over these years I've been suffering from a horrible exhaustion that doesn't go away no matter what I do. And pain that is most times unbearable but I grit my teeth and deal for the time being.
But I'm just looking for some advice I suppose
I’ve only recently come to realize how sad it is to look back on my former healthier self- and not recognize them. As I’ve discovered my chronic illnesses, I’ve learned to miss that person. I just want to be able to run those miles again like she used to.
Whumpee’s been sick. It started slowly, needing more sleep, odd bruises, and unexplained fevers. But the most frustrating part is the clumsiness. Now the whumpee is so tired all the time that they’re always dropping things, falling down a few steps and catching their fingers in doors and the like.
They try to laugh it off and their friends do laugh. They’ll bring it up later as an amusing story and Whumpee smiles along and nods at the more dramatic retellings of coffee spills and silly falls.
But deep down it worries them, this progressing clumsiness, the exhaustion... What is happening to them? They wonder, will they be able to stop it before it’s too late?