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Zoom Meeting for Los Angeles Group #284225 04/21/20 07:52 PM
Joined: Jun 2012
Posts: 651
RAHMBA Offline OP
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You are invited to join the Los Angeles Education/Support Group for our next meeting.
Speaker - Nutritionist Michelle Schirra
May 17th 2pm-4pm

for more information on the group: https://spondylitis.org/resources-support/support-resources/support-groups/los-angeles/

sign up for SAA's eSUN (monthly email spondylitis news) to get the meeting log in information.

Our first zoom meeting in April went really well. so good to see everyone. Interesting to me that 25% said they are feeling less pain while staying at home. 25% worse. 50% the same. people postulated that they are taking better self care while at home. some people are in stressful situations while at home.

The group of 24 people really liked the zoom meeting and so we decided to do this in May with a speaker on a spondyloarthritis topic.

Hope to see you on zoom.


AS, U C, Iritis, migraines. HLA-B27neg. Yoga (instructor) & spin. No meds at this time. Dx 1989. SAA member/donor since 1993. All my posts are personal opinion/feelings and do not represent the SAA. Help find a cure & support others by donating to the SAA.
Re: Zoom Meeting for Los Angeles Group [Re: RAHMBA] #284241 05/08/20 03:15 PM
Joined: Oct 2015
Posts: 389
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Shippingnews Offline
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Joined: Oct 2015
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I am in San Jose. Can I join? Thanks


Male, early 30s. AS diagnosed Sep 2015. HLAB27+
Current medicines: Omeprazole, Vit D3, Celecoxib(1 tab)/Zorvolex(2 tabs)(alternatimg between these two every week), Pyridoxine, Isoniazid, MTX(3 tab) every wednesday, on humira every two weeks since Dec 2015, Weekly Humira since June 18th 2016
On cosentyx 300mg a month since Dec '16
Re: Zoom Meeting for Los Angeles Group [Re: RAHMBA] #284242 05/08/20 04:24 PM
Joined: Jun 2012
Posts: 651
RAHMBA Offline OP
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Absolutely!

Welcome .

Chances are that you won’t be the farthest person on the call :-)


AS, U C, Iritis, migraines. HLA-B27neg. Yoga (instructor) & spin. No meds at this time. Dx 1989. SAA member/donor since 1993. All my posts are personal opinion/feelings and do not represent the SAA. Help find a cure & support others by donating to the SAA.

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