Somatic OCD and Health Anxiety

content warning: MRI results I got prescribed MRIs done on my lumbar and cervical spine over the weekend, and several things came back abnormal in the report. I started to google when I saw a word ending in -oma, got a basic definition of this particular kind of t*mor (probably benign/non-cancerous), realized that googling in this case was for sure a compulsion, caught myself and put my phone away. I told myself, "I have an appointment with my specialist in 2 days. I trust this doctor, so I will delay/not do my own reading until after I talk to her, and only if she recommends further self-education." I stuck to it and I was proud of myself. Cut to the appointmet today. I got lost in the building where her office is and arrived 14 mins late. The receptionist said there's a 15 minute grace period, so I would have to reschedule. No availability for 2 MONTHS, even for telehealth. First of all, I am so ashamed of being late (that's another trigger for me), and so hurt and rejected that they wouldn't talk to me, even very briefly. Now the urge to google is so extreme. There are objectively concerning things in my report, based on what she said ahead of time that we were looking for, and what would affect treatment. I also have a LOT of c*ncer in my family history; 3/4 grandparents, an aunt on each side, and 1.5 bio parents (1 was skin c*ncer, 1 was prec*ncerous polyps removed but considered high future risk to be monitored), so "-oma" and "t*mor" are big red flags in my minds. So while normally I am actually pretty good about living and making peace with my chronic conditions, and health ocd is really only like 5 on my hierarchy, I know that I actually do have to be vigilant about c*ncer in some ways. My balanced solution is sticking to recommended observation scheduling, and then entrusting the research and checking to my trusted providers, so that I am not being negligent nor being compulsive. But now what? I hate waiting. Idk if/when I'll hear from her. Chronic pain in those regions due to curvature and degenerative discs are the reasons I have to get MRIs every couple of years, and now I am so somatically, obsessively aware of that pain and wondering what's going on. This post is a vent, and is my choice to express the anxiety without giving into the desire to google. I'm not seeking reassurance on whether I/my test results are going to be ok. Still, I think just some understanding and/or advice on holding myself accountable for not compulsing would be deeply appreciated. Thanks.

I have gotten maybe about 8 EKG’s within the lest 2 years? I’ve also gotten an echo done, and I got a heart monitor to track my heart over the course of maybe 2 weeks, back last year. Even though I have been to the emergency room so many times because of panic attacks that I thought were heart attacks, and went with a Cardiologist I still obsess and worry. I always think that I am going to develop some kind of heart problem after getting the tests done. Like if they’re just suddenly going to appear/my heart will suddenly have an issue. I especially get nervous when the pain is in the center of my chest + I get a tight feeling like I have pressure on my chest and can’t breathe completely. Please someone share their experience of how they controlled their health anxiety, especially if it’s related to this.

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.