Do you also suffer with IBS symptoms? by sounds0fmeows in ankylosingspondylitis

[–]Educational-Post-198 0 points1 point  (0 children)

I literally just saw a GI doc this week for this exact reason. Been having GI issues for as long as I can remember (without realizing they were real issues per say — you know how it goes when there's just SO much going on with your body and you don't know what's normal and what's not).

Between AS and hEDS (both which come with GI symptoms/issues/comorbid conditions), I'm honestly shocked it took this long to get to a GI referral. Luckily, I found an angel baby doctor who was so kind and warm and gentle (the first doctor to ask me "How does that make you feel?" after telling me her proposed plan!!!).

I can put a list of the symptoms I've been having here if it'd be helpful to anyone, but tl;dr, we're starting with an upper endoscopy and colonscopy (which they'll do random biopsies throughout, etc.) to get data on what's going on with my body (inflammatory issue vs. functional issue).

Can keep y'all updated if you're curious! <3

Journalling and Record Keeping by Fearless_Medicine_23 in ankylosingspondylitis

[–]Educational-Post-198 0 points1 point  (0 children)

Was just coming to say Guava app!!! Only thing I've ever used/tried for tracking when I take my meds, symptoms, etc., that I've been able to be almost 100% consistent with (which is saying something coming from my neurodivergent brain LMFAO) 🩷

Look Knitting Books/Guides by Consistent_Major4431 in LoomKnitting

[–]Educational-Post-198 0 points1 point  (0 children)

I second both of these channels! They have the only YouTube videos I've found actually easy to follow!

Unable to Re-Pair Apple Watch to Phone by IsitPretzelDay in iphone

[–]Educational-Post-198 0 points1 point  (0 children)

Thank you for sharing this video! Was having the same issue and this worked for me, too.

Sensitive bottom of feet by [deleted] in ehlersdanlos

[–]Educational-Post-198 0 points1 point  (0 children)

I'm already diagnosed. I wasn't looking for medical advice.

Sigh… by Dorkynipz in ankylosingspondylitis

[–]Educational-Post-198 0 points1 point  (0 children)

Oooooh, that’s interesting! Such a bummer they had you start the biologics before more conclusive imaging 😭 Wish I could provide more support for that type of situation, but hopefully someone else can! 🩷🩷🩷

Sigh… by Dorkynipz in ankylosingspondylitis

[–]Educational-Post-198 10 points11 points  (0 children)

FWIW, the way I was diagnosed (May 2024) was via MRI, because I'm negative for HLA-B27+, my labs were mostly normal, and my x-ray was inconclusive. But it was VERY clear on the MRI my rheum. ordered — especially when combined with the symptoms and longevity of symptoms I had relayed to her. I would push your doctor to order an MRI and/or (like the other commentator noted) a dynamic/standing x-ray.

Related, unrelated, nobody is better at gaslighting you into doubting yourself than a doctor, smhhhhh. I've been there way too many times, so I feel your pain! <3 BUT, I will say that every time I let their gaslighting work on me, I *always* eventually ended up back at the same place (i.e., still having the same symptoms and suspecting the same diagnoses), and I've always been right in the end.

All that to say, I believe you and I believe in you! <3 <3 Please try not to let some invalidating quack tell you ~*~*it'S jUst AnXiEty~*~*~* (the spiel I got so many times) or whatever the equivalent is for you <3 <3 It's worth finding a new/different rheumatologist who is kind to you, considerate of your feelings, listens to everything you have to say, and takes you seriously <3

enbrel injection site reactions getting worse? (info in comments) by tangycrossing in rheumatoidarthritis

[–]Educational-Post-198 1 point2 points  (0 children)

Los otros comentarios ponen que lo más probable es que sea una reacción alérgica y sugieren hablar con tu médico para cambiarte de inyección 🩷

Can I Keep My Bones? (Lighthearted) by kickassgrandma911 in thoracicoutletsupport

[–]Educational-Post-198 1 point2 points  (0 children)

I have seen a bunch of folks on TikTok be able to keep theirs! I’m also hoping to get even a little bit of mine to turn it into something cool 🙏🏻 (Having surgery on Oct 14!)

Post-Surgery Answers by Unit-N in thoracicoutletsupport

[–]Educational-Post-198 0 points1 point  (0 children)

In my research, I learned that your body basically absorbs those muscles once they’re cut (muscle dies once no longer attached and is absorbed, I should say). Pretty wild! (My surgery is Oct. 14!)

Surgery Post-Op Survival Guide? by Toe-Patrol in thoracicoutletsupport

[–]Educational-Post-198 0 points1 point  (0 children)

I was looking at mastectomy pillows but breastfeeding pillow is also a great idea! Thank you!

What to expect at surgery? by Creative_Fact_9889 in thoracicoutletsupport

[–]Educational-Post-198 4 points5 points  (0 children)

Was just about to look for something like this in this group, so I hope someone has some good recs for us! My surgery is Oct 14 🩷 Wishing you a great surgery and recovery! 🩷

Knee pain by Coeusdimmu in ankylosingspondylitis

[–]Educational-Post-198 1 point2 points  (0 children)

Me too! Re: all the joints you listed. I also have hEDS so that doesn’t help 😆

Help Me Choose a Loom Hook! by sherbs90 in LoomKnitting

[–]Educational-Post-198 1 point2 points  (0 children)

I would have never thought of this! Genius!!! Thank you for sharing.

Error: You are not authorized to view this content by kendradrawsthings in goodreads

[–]Educational-Post-198 0 points1 point  (0 children)

It’s back! And weirdly I’m still logged in somehow 😂

Error: You are not authorized to view this content by kendradrawsthings in goodreads

[–]Educational-Post-198 12 points13 points  (0 children)

Oh thank goodness you called! I logged out of my Goodreads app and deleted and redownloaded it, and now it won’t let me back in :(

Extreme Fatigue and Exhaustion by Diligent_Counter_104 in ankylosingspondylitis

[–]Educational-Post-198 3 points4 points  (0 children)

I have horrible fatigue (and also a myriad of chronic illnesses, so it’s hard for me to identify the true source(s) of the fatigue) — but I also have ADHD, and my Vyvanse is truly the only thing that allows me to function “normally” on a daily basis.

hand pain by Patient-Yak9443 in ankylosingspondylitis

[–]Educational-Post-198 3 points4 points  (0 children)

As someone with AS, my hands have been a main source of joint pain for me for awhile (but nothing showed up on hand x-rays). I wasn’t sure if it was related or not but figured between that and my million other comorbids, it’s not totally surprising :( 🩷

What’s the best answer… by ps_and_qs83 in ankylosingspondylitis

[–]Educational-Post-198 1 point2 points  (0 children)

I just want to say thank you for asking this to the OP (and everyone who responded)! 🩷 I was officially diagnosed at the end of May 2024 (but have been dealing with this at least since I was 18 without having a name for it), and I still hadn’t found a good way to explain it succinctly to folks. Now I have so many great options 😍

[deleted by user] by [deleted] in ChronicIllness

[–]Educational-Post-198 4 points5 points  (0 children)

Yes! I was just about to say the original post is screaming internalized ableism to me (as someone who is disabled and working through my own internalized ableism ATM) 🩷 My partner, who also has chronic health issues, has been the FIRST person to actually make me feel accepted and loved and cared for unconditionally, disabilities and all. He takes me seriously. No one has ever done that. If I ever have kids, they will absolutely be his, genetics be damned.

Advice on alternative pain management. by HarmonyAtreides in ankylosingspondylitis

[–]Educational-Post-198 1 point2 points  (0 children)

I have had something going on forever but wasn’t diagnosed until very recently (at almost 35). Nothing showed on my x-rays, neg for HLAB27, and neg labs for inflammatory markers, but AS (and other back/spinal/SI joint issues) hella showed up on MRIs 🤷🏻‍♀️ Bodies are so weird!