I'm just looking for anyone that is in my province that also has APS. I am pretty confident in the doctors I am seeing in Hamilton, but just looking to see who other people are seeing in Ontario. Thanks!
Anyone here from Ontario, CANADA? - Hughes Syndrome A...
Anyone here from Ontario, CANADA?
Hi, we do have a few Canadians on here, I am sure they will pop up and say hello soon. MaryF
I am in New Hampshire USA --there was a gal from up in your area that use to come on here , hopefully she will see your post - i can't look it up , best to you
Hi,
I have just had a conversation with a woman in Canada who just now put her question on our site, She is looking for help with her HS/APS and help with finding a Specialist who cares and understands and who listens and will treat her.
She did not find your question and asked me to write you this answer.
Kerstin in Stockholm
Hi. I am from Sarnia Ontario, and I would love to know who you are seeing and if they are accepting patients. I have been waiting a year and a half to see someone. But so far nothing. I was diagnosed 12 years ago, but current problems resembling MS cause me to fall when I am walking or standing. Are you happy with your doctors?
I just replied to your post...
Hi there - very late to your APS party, but here I am! Just diagnosed in November of 2023 after a mild stroke in May 2023. I'm trying to manage warfarin (so far a nightmare), and my stress (even worse). I would love to know how you're doing 7 years on!
hello. I am in Toronto. I was diagnosed in Sept 2022 after a possible TIA. I am looking for a doctor. Could you tell me who you are seeing in Hamilton? How are you doing? Thank you.