Am I undiagnosable?
So I'd randomly get joint pain and still do but it was much more random in the beginning. Most of the time it was diagnosed as tendonitis and healed within 6 weeks. If I walked for half a mile more than I was use to my knees would begin to crackle and I'd get a really bad migraine from walking in the sun. both my Patellas are tipped but I haven't had any crackling since September.
I started weightlifting in 2022 and I would still randomly have joint pain but I'd stop going to the doctors around 2023 because my rheumatologist said only come back for an unexplained rash, swelling or fever and I don't have a thermometer. When I rashed up I wasn't in any pain and my mom forgot who my doctors were so I kinda ignored all that. and kept weightlifting.
I noticed that the working joints that weren't in pain would help the injuries or whatever heal faster. But then in September I started feeling like I'd just flare up from any form of resistance. I went from repping a 135 squat to pain and cracking from a bodyweight squat. I also had chest pain, and a bruise on my left ankle that suddenly became very painful. Went to my Ruem finally. No rash, swelling or fever. Sent home with a diagnosis of costocondritis and flat footedness.
I never really had an issue with flat feet like my dad or brother. Unless we count every bout of ankle pain of course. I asked my PCP for disability because I just stopped working and leaving my bed for the most part. She said to ask my Ruem. He said it's her responsibility but the only accommodations he could offer were moving as much as possible. To which I responded "I am" But he gave me my paperwork and sent me home.
Went to my PCP and she said she couldn't offer anything because there was no abnormality in my joint and I'm negative autoimmune disease. At the time and currently I am biasing my knees. I finally got an X-ray after like 6 months of complaining and my kneecaps are misaligned.
I just switched PCPs around October because my old PCP gave me an inhaler and diagnosed me with asthma for my costrochondritis which made me feel terrible. There's not much places to go for healthcare with state insurance. They're telling me to move but I'm already doing what I can cause I'm scared to atrophy. When I could still work I'd eat salmon, chicken, beef, fruit, candy, cereal and a little veggies and that was most of my diet. They blamed my low cholesterol on a shit diet. My vitamin D basically halved in the last 3 months and that's just diet. Idk how I'm supposed to eat well and exersize if I can't always muster up the energy to acquire capital or exercise.
Oh and now if it's too sunny and I go outside for 15 mins+ I'll feel nauseous and lightheaded and get a migraine and vomit if stressed in anyway including walking or hearing a baby cry.