Yes I do… thankfully..

This is fabulous!! ❤️ thank you, I really do appreciate your kind comments ❤️ New Zealand is literally 10 years plus behind the rest of the world medically…

This is a brilliant paper!! Thankyou!! I’m so pleased I listened to my body especially when my tastes told me food or drinks tasted like chemicals.. I’m only drinking water and hydrate!!

Thankyou. I do also have long covid… 2022 lost my smell and hasn’t come back!!

Thankfully I kept my ovaries.. they were however twisted with my uterus, bladder and abdominal wall into my left pelvic wall, with endo, adhesives had taken over in there.. add HPV that I never knew I had and abnormal cells… with a fibroid in my uterus. It’s been amazing lifting my left leg!!

Yes an and ANA and HsCrp… the real baseline bloods…

Yes I’ve been reading about the tests showing negative, yet can possibly still be positive. I’m judging wanting to find anyone in the medical community that enjoys giving answers to the citizens of the world that can’t pay the expensive medical tests and care ❤️

I was surprised to wake up from surgery with a purple hand up to my wrist.. thought I had knocked it some how.. confirmation from my amazing gynaecologist said my hands were tucked away and no injury accorded… last time I had inflammation, was 2016, when my gall bladder got removed in parts.

It’s the public system… so the basic of basic because as I got told when I put in a complaint “arthritis is our bread and butter” so they didn’t want me even in the building…

Fabulous ❤️❤️ definitely supporting documents count.

When you turn up with printed evidence from medical research… there isn’t much more to add. :-) that is how I approach all medical issues now. Like you I’ve been dealing with “it can’t be”…. It’s frustrating.

I hope you have supporting letters from everyone else stating that? Also pull up all the evidence on pubmed :-)

Apologies, definitely not invalidating your experience… the world health system is using and abusing everyone with health concerns. ❤️

That isn’t too bad… I had 2 rheumatologist appointments where they didn’t actually expand their tests, just a sad attempt at poking my shoulders and when I didn’t want to up my current meds, they said goodbye… Im fairly certain I have sine scleroderma.

Why do you have to wait? Will it make a surprise remission and disappear? Lol