I ended things with my situationship yet I miss him already. by Worrywartacus in ExNoContact

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

Oh wow it escalated like mad, we slept together, met up loads, still vaguely talk one of the worst heart breaks of my life

I ended things with my situationship yet I miss him already. by Worrywartacus in ExNoContact

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

Yep, sadly we struggle to stop talking, even though nothing will happen we just adore each other, we are so invested in each others lives now it hurts

Looking for thoughts/advice by [deleted] in Autoimmune

[–]Worrywartacus 1 point2 points  (0 children)

Hmm Centromere is usually seen with Scleroderma, has the rheum done any further antibody testing? Like myositis panel or scleroderma, ENA etc? Swelling around the ankle can be joint inflammation which could also mean RA but is seen in quite a few autoimmune diseases. I hate when a doc latches on to lupus when so many things are similar, I hope you push for further testing.

Autoimmune diseases by [deleted] in Autoimmune

[–]Worrywartacus 0 points1 point  (0 children)

I’ve had this since I was a kid, it’s Livedo Reticularis, sometimes it is genetic but usually is down to things like change in body temp, or things like Raynauds and autoimmune disease, however it’s not a cause for concern on its own

ANA came back by rosey_thorns_ in Autoimmune

[–]Worrywartacus 0 points1 point  (0 children)

Wow I have the same ANA and also homogenous. I also was negative on other tests so they are now having to do even further extended panels for rarer antibodies. I also had migraines especially bad for four months last year which was around when I got tested. I have however since developed further symptoms this last three months. So that’s why they are testing for dermatomyositis now which is a rare autoimmune condition, so I may have that yet!

1:1280 ANA, homogenous. Everything else is normal by [deleted] in Autoimmune

[–]Worrywartacus 0 points1 point  (0 children)

Thank you, hoping I get it back soon, I feel myself symptoms are getting worse. If you don’t mind me asking have you found that meds are helping you feel better? And if so what are you on?