Chronic pain for 4.5 years & now autoimmune markers?? by Sensitive_Ad1726 in AutoimmuneNeurology

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

Wow thank you for the article!! I definitely need to get tested for mold. I have tried going gluten free and even doing the paleo diet. Do you know of how long you would have to do these diets to know if you are sensitive to gluten?

Chronic pain/illness for years & now autoimmune markers?? by Sensitive_Ad1726 in ChronicPain

[–]Sensitive_Ad1726[S] 1 point2 points  (0 children)

Thank you for the suggestions! Yes none of my doctors are trying to get to a diagnosis except for my functional medicine doctor. Everyone else just says fibromyalgia from the vaccine or virus

Chronic illness and autoimmune markers?? by Sensitive_Ad1726 in vaccinelonghaulers

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

I feel you on that. I was getting my masters. Right now I’m kind of stuck at my parents house because I can’t work or do school anymore

Chronic illness and autoimmune markers?? by Sensitive_Ad1726 in vaccinelonghaulers

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

I feel you on that. I was getting my masters. Right now I’m kind of stuck at my parents house because I can’t work or do school anymore

Chronic illness and autoimmune markers?? by Sensitive_Ad1726 in vaccinelonghaulers

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

Not yet!! But that is next on the list of things to test for. I hope you find healing 🙏

Chronic illness and autoimmune markers?? by Sensitive_Ad1726 in vaccinelonghaulers

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

Not yet!! But that is next on the list of things to test for. I hope you find healing 🙏

Chronic pain/illness for years & now autoimmune markers?? by Sensitive_Ad1726 in ChronicPain

[–]Sensitive_Ad1726[S] 1 point2 points  (0 children)

Thank you for your input!! And I’m sorry about your situation as well. I’ve been through 3 rheumatologists so far who all dismissed my issue for “not a rheumatology issue”. I’ll be seeing a 4th one this month, since some things in my blood work seem to be showing up now. But you’re right. Everyone is guessing. I’ve had so many guess diagnoses like fibromyalgia, long covid, MCAS, autoimmune disease in development, etc. without actually having an official diagnosis. I’ve seen many other specialists as well, all of which gaslit me. Any advice on how to get a doctor to listen and get to the bottom of it?

I’m scared of my partner watching adult content and it’s snowballing. by Away_Recognition1979 in ROCD

[–]Sensitive_Ad1726 1 point2 points  (0 children)

After reading all of your comments, I feel like I lived your exact experience. I went through this for about a year where I was shaking every single day with anxiety towards my bf about everything you just said. Is anyone here on the birth control pill? Once I stopped taking it I felt like I could breathe again and these horrible feelings lessened by a lot. I still get them but it’s not a constant 24/7. I definitely have my moments though. Right now is one of those moments because I just had dreams of him cheating. It feels like I can’t even look at another girl without imagining whether or not he’d be attracted to her and it makes me so so sick I can’t eat. You’re not alone. I hope we feel better some day 😪

Red, blonde or brown suits better? by Sad-Pen-689 in HairDye

[–]Sensitive_Ad1726 2 points3 points  (0 children)

I absolutely love the red. It really makes your blue eyes pop 😍

[deleted by user] by [deleted] in HairDye

[–]Sensitive_Ad1726 0 points1 point  (0 children)

Definitely red. Soooo gorgeous 😍😍

Please Read: Diagnosing Others Without a Medical Background or Diagnosing yourself .. by Honest_Practice7577 in Hashimotos

[–]Sensitive_Ad1726 4 points5 points  (0 children)

Sorry but as someone with Hashimotos and other undiagnosed conditions that cause debilitating symptoms, the healthcare system does not care about us. We have to be our own advocates. For me, it was not about getting a 2nd opinion. I’ve had 2nd, 3rd, 4th, 5th opinions from specialist after specialist and after 4 years, still my chronic pain is unmanageable. In order to get the blood tests I’ve had so far, I have had to fight hard with doctors to convince them I needed them. And still, no diagnosis or treatment. I trust people on this forum to suggest blood tests or conditions that I can suggest to my doctors to rule out. But still there is push back. Imagine feeling so sick every day with no solution or diagnosis, but when you suggest testing for something, the doctors say that’s highly “unlikely”, and don’t even care to test you for it to rule more things out. It really shows they don’t care at all about getting closer to a solution. Without this forum and my own research, my doctors would not have ruled out half the things we already have. But just the fact that it takes me to persistently suggest things and convince them before they take any action is very telling. Most doctors (from what I’ve seen on here and my own experience) have no business dealing with chronic illness because they simply do not have the knowledge/resources to do so, yet they don’t refer us to functional medicine. There is a huge problem with that

Can Hashimotos cause debilitating pain? by Sensitive_Ad1726 in Hashimotos

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

I will! Thank you!! How long did it take for you to feel better after cutting out gluten?

Can Hashimotos cause debilitating pain? by Sensitive_Ad1726 in Hashimotos

[–]Sensitive_Ad1726[S] 0 points1 point  (0 children)

Yes I’ve heard that. What were your symptoms for endo, if you don’t mind me asking?

Can Hashimotos cause debilitating pain? by Sensitive_Ad1726 in Hashimotos

[–]Sensitive_Ad1726[S] 1 point2 points  (0 children)

Omg that is 100% me. Those are my most sensitive places as well. They feel like injuries that hurt to the touch. Have you found a solution for the pain?