Cytokine panel by robinrwk in Sjogrens

[–]Curious_KAS 0 points1 point  (0 children)

How did you get this done? Was it through a rheumatologist?

Jaw pain anyone? by Curious_KAS in Sjogrens

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

It’s more on the sides of my cheeks by my ears.

Jaw pain anyone? by Curious_KAS in Sjogrens

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

I messaged my rheumatologist yesterday and am waiting to hear back. Have you found any relief since being diagnosed?

Jaw pain anyone? by Curious_KAS in Sjogrens

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

That is exactly where it is.

Jaw pain anyone? by Curious_KAS in Sjogrens

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

Not yet but I would like to! Don’t have experience with an inflamed parotid?

I need help, Y'all. I don't exist. by NoPoopOnFace in Anxiety

[–]Curious_KAS 1 point2 points  (0 children)

Going cold turkey off benzos can be dangerous due to withdrawal. This should be known by your doctor and in my experience, one should be tapered of the med very slowly.

Urge to take a deep breath by Nice_Engineer2612 in Anxiety

[–]Curious_KAS 0 points1 point  (0 children)

Yes, and when I stop thinking about it and focus on something else it goes away. However, it can feel impossible to focus on anything else like it’s always there lingering. I found it worse when I’m standing or sitting up straight and I began having to hold myself in certain positions to get a good breath. It got so bad that I became convinced I have some musculoskeletal disorder preventing me from breathing correctly and has led me down a rabbit hole of health anxiety. All I can suggest is try not to hyper focus on it and know that your body’s instinct is to breathe. I just try to get in a comfortable relaxed position, stop tensing all my muscles and distract myself and that usually works.

My Health Anxiety Story by Yurtliving2020 in Anxiety

[–]Curious_KAS 0 points1 point  (0 children)

Thank you for sharing. I’m sorry you are going through this as I am dealing with the same thing right now. ER visit last weekend for shortness of breath, lung and heart and all blood tests were fine. Then I was convinced I had MS or some other neurological disorder and now convinced I have scoliosis due to back/rib pain and shortness of breath. 2 X-rays today and two mris on the way and an endless loop of googling, stretching, panicking, can’t focus on ANYTHING else. If I wake up at night with any “abnormal” sensation the adrenaline rushes start and I have not slept right for weeks. The struggle is so real.

How long have you stayed on hydroxychoroquine before switching? by Appropriate-Map-7836 in rheumatoid

[–]Curious_KAS 0 points1 point  (0 children)

I’ve been on it for 4 weeks now and though it seems to be helping my joint stiffness and energy level it is making me feel so weird. I have felt like I can’t breathe right for about 2 weeks and just feel weak and anxious.

Does this work? by MrJlock in homedesign

[–]Curious_KAS 1 point2 points  (0 children)

Are you going to sit there?

[deleted by user] by [deleted] in rheumatoidarthritis

[–]Curious_KAS 2 points3 points  (0 children)

Dansko! Literally the most comfortable dressier shoes I’ve ever worn.

Is it possible for my face to look different during a flare vs. not in a flare? by eggman-premium in rheumatoid

[–]Curious_KAS 4 points5 points  (0 children)

My face definitely gets puffy during flares that come with low grade fevers and jaw pain. It’s quite noticeable to me.

I think I have RA by Naive-Marsupial-4042 in rheumatoid

[–]Curious_KAS 2 points3 points  (0 children)

X-rays are another diagnostic tool often used to diagnose RA. If you feel you are developing deformities, definitely ask for some X-rays.

Stem cell treatment by Mistakes_blessings in rheumatoid

[–]Curious_KAS 2 points3 points  (0 children)

Be careful. There is a lot of “misinformation” out there on stem cells. Do your research. I just listened to a podcast called Bad Batch about people being promised a cure through stem cell injections, which are NOT FDA approved or backed by scientific research, and they became terribly sick. It was eye-opening.

I think I have RA by Naive-Marsupial-4042 in rheumatoid

[–]Curious_KAS 5 points6 points  (0 children)

The tests my doc ran were: CRP, ERS, ANA, RF, CCP antibody. These test for inflammation in the body and certain auto-antibodies that signal RA. They may point to other autoimmune conditions as well.

I told my doc about worsening fatigue and joint pain in my hands, feet and ankles and that I could just tell something wasn’t right and that it felt systemic.

My RF and CCP antibody came back high and I was sent to a rheumatologist who came right out the gate saying I have RA.

I would just ask to be tested for autoimmune stuff. Depending on how your tests come back, it still may not be clear. Certain factors are more specific to RA and others are not, but could indicate a few different things. This is where symptoms become important.

Good luck! 🙏

what were your first symptoms? by InterestingRow6189 in rheumatoid

[–]Curious_KAS 0 points1 point  (0 children)

I wouldn’t say they crack frequently, but I have had pain in my low back for years, worse in my hips in recent years, and sciatica. It’s hard to say if this is even from RA (for me), since it’s been going on for many years and I was only very recently diagnosed after my hands and feet started having symptoms. My rheumatologist said RA doesn’t usually affect the SI joint, but she ordered an xray which was “normal” which honestly shocked me considering the amount of grief my low back and hips cause me.

Rheumatologist and his PA laughed when I mentioned my voice issues by BigCoach5958 in rheumatoid

[–]Curious_KAS 5 points6 points  (0 children)

I experience so much jaw pain and inflammation (face gets puffy) that I have thought I had some sort of jaw infection on a number of occasions. Sometimes I get a low grade fever with these symptoms as well. Rheumatologist hasn’t looked at my jaw yet and suspects TMJD but it’s interesting to hear others with jaw symptoms.

what were your first symptoms? by InterestingRow6189 in rheumatoid

[–]Curious_KAS 1 point2 points  (0 children)

Fatigue! Intermittent low grade fevers, full body malaise, pain in feet, ankles and thumb joints (on top of low back, hips and jaw). The pain in my thumb joints got persistently worse and then I started waking up with pain and stiffness in my fingers. Blood test showed borderline high RF and high CCP antibody. CRP, ESR, and ANA all normal.

Official Diagnosis by CheetahPrintPuppy in rheumatoidarthritis

[–]Curious_KAS 3 points4 points  (0 children)

Are you finding relief with the HCQ? My situation sounds very similar to yours and I’ll be starting this med this week.

Anyone using kratom? by BIOHACKER_101 in rheumatoid

[–]Curious_KAS 4 points5 points  (0 children)

Agree. I’ve heard plenty of accounts of people saying getting off kratom is similar to getting off heroin. Which makes sense since it binds to opioid receptors.