- User type
- OCD Conqueror
- Date posted
- 1y
Health OCD
Hey!! I have health OCD wondering what everyone else struggles with and how you cope with things? Just seeing if there are similar story’s out there! 😊
Hey!! I have health OCD wondering what everyone else struggles with and how you cope with things? Just seeing if there are similar story’s out there! 😊
I also have health ocd!! mixed with a few others haha. I struggle pretty hard with the aspect of always thinking there will be some form of illness or infection, and I will be too late to catch it. I’m still on the learning how to cope end of things. I luckily have a very kind partner who will talk me down when I start to spazz. I have to refrain from giving into my compulsion- it gets 10x worse when I do lol
@alyssaw Thank you for sharing!!! If I have a pain in my chest which is normally caused by my anxiety I resort to the worst thing possible and spiral out of control. You are lucky to have a partner that understands!!!
I convince myself atleast 2-3 times a week I'm dying. I will freak out about if I'm having a heart attack, stroke, or any other random thing.. I usually just spiral and freak out until I either come to peace with dying or just convince myself I'll be ok. It's not great coping mechanisms really but I haven't found anything else that eases the paranoia/anxiety.
I’m 19 and struggle with health anxiety, contamination, harm, and magical thinking OCD and would love to meet people with similar experiences and hardships because I have never had an opportunity for such a supportive community!
Hi everyone! I’m feeling better today. I had a really bad flare yesterday, my husband really helped me calm down and fall asleep. However, if you have health OCD I feel like you probably shouldn’t read this post unless you are in a good head space. I do not have health OCD. So, I’ve been dealing with a lot of symptoms and health issues that have led me to alot of doctors visits, I have several different doctors that specialize in specific things and now go to an internal medicine doctor. My doctor thinks I have an autoimmune disease, so I’m running alot of tests for several different autoimmune conditions. My OCD has been dormant for a while. I would still deal with it sometimes, but it was way easier to manage. I’m not medicated for OCD. However, I do use arthritis cream and was prescribed muscle relaxers, I have not yet taken the muscle relaxers. So I had a really bad OCD flare last night, specifically Relationship OCD. My husband has just seen parole and I’m super excited for him to come home, but my OCD was trying to convince me otherwise. I also have a new nephew that was born on the 22nd. So I am out of state and was watching my niece for my sister in law. A lot of exciting things happening at once. I’m assuming that triggered my OCD. But I’ve been swelling in my face and dealing with a little bit of body pain as well. Autoimmune diseases come in flares like OCD. I have done some research on autoimmune diseases so I can know what I need to do in order to keep it under control if that’s what I do get diagnosed with. I learned that some autoimmune diseases are linked to OCD, or can even cause OCD because of inflammation in the brain. & It gave me a glimmer of hope honestly. Could my OCD have started because of an autoimmune disease? Could I get better by treating it? My OCD didn’t kick start until I was about 19. I am now 23. I did have symptoms of OCD at 17 though, I went through a period of time where I was compulsively praying and in a cycle of intense anxiety. So I probably had it since I was 17, but I don’t know. My symptoms of autoimmune disease didn’t start until about a year ago, but it could’ve been longer. I couldn’t get rid of a UTI I had for MONTHS & didn’t know why. I had to see a urologist, I was 21 when I kept getting UTI’s. I had to get a procedure done, I had pus build up in my urethra that was almost completely blocking off my urethra. I do not know how the infection got that severe.. especially because I took antibiotic after antibiotic. I felt like I’d get better for a few days, then boom…UTI symptoms once again. So.. that could’ve been the start of autoimmune symptoms. With an autoimmune disease, your immune system is pretty trash. You don’t fight off infections or illness as easy as others. I remember how I’d get sick after everyone else in the house would get sick, but I’d get it so much worse and have the illness for much longer than everyone else. Surprisingly enough, I never got COVID. My whole family had it & I didn’t get it. Unless I did and just didn’t have symptoms. Anyways, I never thought I would say this.. but I hope I do have an autoimmune disease that caused OCD so that I can treat the autoimmune disease and keep my OCD dormant for as long as possible. I forgot what it was like to deal with OCD.. it was so bad lastnight, I remember feeling that type of anxiety and it’s the worst.. 💔 If you took the time to read, thank you! I seem like a charity case lol.. I never thought by 23 years old I’d be like this.
You can laugh at the title if you want, it’s objectively pretty funny. Hi guys, this is my first time on this app and I mostly just wanted to see if anyone out there is in the same boat as me or works in health care and is dealing with this. I haven’t told anyone what’s going on. I’m in my 4th year of medical school and In the past year I’ve developed what I think is pretty bad health OCD. Now health anxiety is a really common thing for medical students to have, I know that. It wasn’t until recently that I realized that the constant lymph node checking, self diagnosing & examining and reassurance seeking could have definitely had crossed the line into compulsions. Both my parents are cancer survivors which is what originally made me want to become a doctor but now every single physical sensation I have sends me into hours or days of rumination that I or someone I love has stage 4 terminal cancer. I spent an entire vacation with my boyfriend having a silent panic attack and convincing myself that he was dying of pancreatic cancer when he just had food poisoning and was fine days later. I had a complete mental breakdown and told myself I had lymphoma for weeks when I realized I could feel some of my own perfectly normal lymph nodes in my neck. My logical brain knows this is completely ridiculous but the emotional brain will not shut the hell up. It seems cruel that I made it this far only to feel like my own damn brain is betraying my ability to think through health situations clearly. I’m determined to get my symptoms under control before I graduate in a year as I don’t want this to affect patient care. Just wanted to get this off my chest and see if anyone else out there in health care is struggling too.
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