Physical symptoms? Last year I had terrible physical ailments: brain fog, super nauseous, felt like fainting, dizzy, fatigued, chest pain, etc. It didn’t seem to change with diet and I got alllllll the tests which found nothing. It went on for probably 6 months. Then my OCD flared up in an old theme and the physical symptoms basically went away. I was just suffering severe mental distress. Since doing ERP and breaking free from that (thank you, Monique!!) it’s been a few months and I am having some of those physical symptoms again. Can anyone relate?? Is it a subconscious OCD thing to manifest physically? I am certainly anxious about the symptoms when they’re happening because they’re intense, but I don’t feel anxious before they come on.

Hi!! My names Calista R. Woodbury-Rabon. I recently got married in March of this year. And have been struggling with my severe anxiety disorder since I left my toxic 3 year relationship about a year ago. Over the past several months, I have noticed that I go through phases where: I have a full body “anxiety attack”. Or at least that’s what I call it. For example : when we went to cookout and they told us they were out of the chili for walking tacos. I had a full blown anxiety attack or at least what I thought was an anxiety attack and starting hyperventilating and crying. Therefore, the only solution (in my mind) was that I wouldn’t be able to calm down until I had the walking tacos. Another example : My husband bought me a pajama set that was only recently put out because it was a patriotic item which means that after the summer it’d be gone… I ended up picking up the wrong size. So that night when I went to put on the Pajamas and realized they were too small I started hyperventilating and crying. All because these $17 pajamas did not fit me and it was no fault of my own. Whenever this happens, I usually end up spiraling and crying and saying a lot at once very quickly. And I usually look crazy and don’t make a lot of sense. Usually after the spiraling is over with I’m very exhausted and usually will cry myself to sleep. My husband more often than not will say stuff like “it’s not that big of a deal you can get something else.” << when it has to do with food etc. OR “we can just buy another set of pjamas the next time I get paid.” << in relation to the pajamas in this instance. But honestly no matter what him or anyone else tells me in that moment. All that matters is that I can feel the anxiety in my bones. And I can’t breathe and in that moment my world as I know it has ended. I’ve tried taking online free “quizzes” to find out if I acctually have OCD and they’ve been negative. I also did some research and learned that you can have all the symptoms for a OCD “flare-up” but present no active case of OCD or symptoms. So I guess what I’m trying to find out is if I don’t have “OCD” than Is this out of body experience caused from my “severe anxiety disorder” diagnosis ? Or just anxiety in general?? Thank you for taking the time to read this even if you also aren’t sure!! Means a lot to me..❤️‍🩹

Hi I’m new to this group. I’ve had ocd and very bad anxiety disorder since I was a kid and only got progressively worse as I grew up. I’m 26 now. I had some somatic/sensorimotor ocd while growing up and feeling or worrying about health concerns that aren’t actually there… anyway about 5 weeks ago I randomly started feeling like I had to go pee all the time? I don’t have any pain or anything just the horrible constant feeling like I need to go pee. I’ve gotten checked for a uti multiple times. My pcp suspects it could be being exacerbated by the anxiety because it’s so distressing to me it’s almost all I think about. My ocd has convinced myself that I now have some chronic bladder problem. I notice it’s not as bad at night when I’m relaxed (thanks to medication) and about to fall asleep. I just am so scared that it’s never going to go away and I’m going to have to deal with this for the rest of my life and I can’t do that…. Was just wondering if anyone else ever dealt with this symptom? I know our brains are powerful but sometimes it just feels so real. 😣😣

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.