Scleroderma Foundation - MN Chapter
@SclerodermaMN
The Scleroderma Foundation Minnesota Chapter is a #nonprofit serving as a voice for those in Minnesota living with or affected by #scleroderma.
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“Our study is one of the first to report mental health symptom changes during #COVID19 in a vulnerable population with a pre-existing medical condition and the first to compare symptom changes across countries." sclerodermanews.com/2020/10/06/cov… #scleroderma
This weekend we hosted our virtual Patient Education Conference and we are so grateful to all who joined us! A special thank you to Dr. Jerry Molitor and Dr. Joanna Harper for your engaging, informative and enlightening presentations! #scleroderma #sclerodermaawareness
Shopping AND giving back? Yep, you can do both! Make a difference while you shop #PrimeDay deals on 10/13 & 14. Simply shop at smile.amazon.com/ch/41-1802254 or with @amazonsmile ON in the Amazon Shopping app and AmazonSmile donates to #Scleroderma Foundation Minnesota Chapter.
We couldn't bear the thought of skipping this year's Patient Education Conference, so we're taking it virtual! Mark your calendars for 10/17. The event will take place on Zoom from 10AM-12PM. Stay tuned for more info!
Register for this awesome event!!
Happy #NationalNonprofitDay! We are proud to be a #nonprofit organization dedicated to making a difference in the lives of #scleroderma patients and their families, and we're thankful for you and your support so we can keep doing the work we love!
It's #WellnessWednesday! Did you know that there are #yoga practices specifically for people with scleroderma? Check out this site for yoga poses catered to those with #scleroderma! yogaforscleroderma.com/home #wellnessmonth
August is #WellnessMonth! We know it is difficult, uncomfortable, and sometimes downright impossible to exercise when you're suffering from #scleroderma. But @sclerodermaUM has some #exercise guidelines in this great video: bit.ly/3icspzr
Not today, #COVID! Although all in-person support groups have been cancelled, we are continuing to host regular virtual support groups. Contact a group leader for more information. bit.ly/3hIRVvL #scleroderma
Did you know that @SclerodermaNews has a page specifically dedicated to providing COVID-19 updates and resources for #scleroderma patients? And it's updated weekly! Check it out at sclerodermanews.com/information-ab…
#Research Update! “This study is truly a landmark, in that it will share our experience at UNM successfully treating children with #scleroderma in this safe and novel way, and will likely help children with this rare disorder around the country." sclerodermanews.com/2020/07/06/ore…
Use your voice and join us for the National Day of Action on June 29! We want a cure, we NEED a cure. #scleroderma #sclerodermaawareness #sclerodermaawarenessmonth
Suzy Ballantyne, Co-Chair National Scleroderma Advocacy Committee & Tri-State Board Member shares How you can get involved in National Day of Action. Never underestimate the power of one voice. Your voice! Scleroderma.org/NationalDayofA…
We're just TWO DAYS away from the virtual #SteppingOutToCureScleroderma walk in the Twin Cities! Join us by sharing your selfies on Sunday with #MySteppingOutSelfieMN!
I mean, come on. Does it get much cuter than this?! Little Sophie is ready for the virtual #SteppingOutToCureScleroderma Walk on Sunday! There's still time to register/donate at scleroderma.org/steppingoutmn. And don't forget to share your photos with us using #MySteppingOutSelfieMN.
Who has Stepping Out spirit? Amy has Stepping Out spirit! How are you participating in the virtual #SteppingOutToCureScleroderma virtual walk on 6/14? We want to see! Share your photos with us by using #MySteppingOutSelfieMN. Register and donate at scleroderma.org/steppingoutmn!
Who's out there walkin' for #scleroderma awareness? Elaine and Zoli are! Elaine is a Scleroderma Foundation - MN Chapter board member and the West Metro Support Group leader, and they're out there sharing their #MySteppingOutMNSelfie!
We can’t find a cure without YOU! Join us virtually on June 14th for the 2020 Stepping Out to Cure Scleroderma Walk! Wear your teal shirt and hit the streets, the backyard, the treadmill or the kitchen. Props to the most creative participants and outfits! #MySteppingOutSelfieMN
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World Scleroderma Foundation
@Worldsclerofnd -
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