Anyone here from Ontario, CANADA? - Hughes Syndrome A...

Hughes Syndrome APS Forum

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Anyone here from Ontario, CANADA?

jaymacz28 profile image
7 Replies

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!

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jaymacz28 profile image
jaymacz28
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7 Replies
MaryF profile image
MaryFAdministrator

Hi, we do have a few Canadians on here, I am sure they will pop up and say hello soon. MaryF

jetjetjet profile image
jetjetjet

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

Lure2 profile image
Lure2

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

snorkle272 profile image
snorkle272

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?

jaymacz28 profile image
jaymacz28

I just replied to your post...

MJTroubadour profile image
MJTroubadour

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!

dillty profile image
dillty

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.

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