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@pb50

SERIOUSLY GREAT FORTUNE. when I was first diagnosed I lived in NYC working as Chief of Staff to a senior exec at the bank and that level of Officer had their own clinic so they could just run upstairs if they needed a doc. I couldn’t take notes in meetings or even open my own water bottles- so he asked the upstairs head of medicine and the next day I saw one of the best rheumatologists in the city. And a woman to boot. When I moved to NC she found a referral for me (after the one I found on my
Own told me I had OA, not RA. Until that point I had never tested positive for RA factor,
But when that jerk tested me to prove I didn’t have it, damned if I didn’t. That was my mother in heaven saying “I’ve got this”. 🙂
But yes, freakish good luck.

I am going to wait for the CT to see if it notes adhesions or significant inflammation but it’s not out of the question to me that it’s an inflammatory reaction.

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Replies to "SERIOUSLY GREAT FORTUNE. when I was first diagnosed I lived in NYC working as Chief of..."

Loved reading your story, Pam (@pb50 ). Have to agree that finding a specialist able to understand you and what you need is a very fraught journey. And in this instance I do mean 'journey' - sometimes it feels like you've been to Mongolia and back. I can relate - also being RA factor -ve, and having had one rheumatologist tell me 'nothing wrong with you, although you have OA in your big toe'. (!) Finding a great rheumatologist really is the key to both the right treatment and feeling good about yourself. I feel as though I can cope with anything RA and Fibro throw at me if there are empathetic people around who don't make you feel like a fraud. Good luck with the CT - hope it's something identifiable and treatable. FWIW, my Fibromyalgia manifests sometimes as pain and tightness around my ribcage that feels like it's restricting breathing so there really are a whole truckload of 'maybe's. Fingers crossed for you. x