Listen to a podcast about #smas CBC Podcasts cbc.ca/listen/cbc-pod…

New Zealander needs to travel to Germany for surgery. ⁦@MedCouncilNZ⁩ why must your people fundraise for these #lifesaving surgeries #raredisease #help #nottooraretocare givealittle.co.nz/cause/health-s…

Anorexia Nervosa and Superior Mesenteric Artery Syndrome | Psychology Today #GITwitter #MedTwitter #raredisease Psychology Today psychologytoday.com/us/blog/the-ne…

PURPLE | Tonight for Annual Superior Mesenteric Artery Syndrome Awareness Day. SMAS is a rare digestive condition affecting 0.013-0.03% of the worldwide population. For more information please visit: smasyndrome.org

A good friend from our SMAS community passed away on Thursday. This is the 4th person this year. For a rare disease where we are regularly dismissed by the medical profession we only ask that Doctors do better! #raredisease #Gastro #curegp

The chronic and unpredictable nature of #IBS can disrupt daily routines, work, and social life. Many may be afraid to discuss their symptoms due to the private nature. If you have a loved one with IBS, here are some tips to remember #IBSAwarenessMonth #IBSDilemma

Visit us at Booth 931 during #DDW2024 to learn about #SMAS #GItwitter

Young girl in #SouthAfrica needs revision surgery for #SMAS Please retweet to help family with #fundraising smassouthafrica.co.za/?fbclid=IwZXh0…

Rana is a 22 yo who needs help! Rana's last chance for recovery gofund.me/a9e85da2

Prayers from around the world for 13 yo Seanna Potgeiter who undergoes her 3rd surgery for SMA syndrome. Her family funded surgeon from USA to travel to South African Government to assist in surgery. USA TODAY Fox News #raredisease facebook.com/profile.php?id…

So grateful to our medical advisor Domingo Alvear, MD for continuing to change lives! American College of Surgeons contact us to learn about this procedure #saynotoDJ Seanna looks at food differently after over R200k surgery for a rare syndrome citizen.co.za/fourways-revie…

This is Rana- she is struggling to stay alive. Rare disease is not political. mondoweiss.net/2024/11/fighti…

We're exhibiting at #DDW2025! Meet us there to see what’s happening — and what’s coming — in digestive disease care. Register by April 30 to save: app.ingo.me/q/b1mln

Looking forward to attending #DDW ! This is our 2nd time attending and we are excited to talk about SMAS with #gastroentrologist #GI Gastroenterology American Gastroenterological Association (AGA) society for surgery of the alimentary tract Gastro Girl

Ready for day two of #DDW Come visit us at Booth 5222 to learn about #SMASyndrome and get your ducks in a row #NotTooRareToCare

Last day at #DDW2025 Visit our booth 5222 to learn about SMASyndrome! #GI #gastro #gastrovascular #rareisreal

The SMAS Nonprofit is partnering w/ IFFGD for Virtual Wellness to raise funds for #GI research #moves4GIhealth

Manitoba woman prepares for life-changing surgery in U.S. after years of rare health struggles #surgery #gi #raredisease #smas classic107.com/articles/manit…