Zeal Access

Unexplained epilepsy seemingly sounds self-evident, but it encapsulates so much more.​ ​ Swipe through for 4 key things to know about unexplained epilepsy, and how exome testing can bring you or someone you love closer to diagnosis.

CACHE Minute: Building a Website for Your Patient Advocacy Group youtu.be/SjIaQR9mI5A?si… via @YouTube

On our way to #SanDiego for @GlobalGenes #RAREAdvocacySummit #GGSummit23

Are you joining us for the RARE Advocacy Summit, Sept. 19-21? Make sure you stop by and say hi to our exhibitors! If you aren't able to join us in person, tune in to our livestream: go.globalgenes.org/ras-x #WeekinRARE #RAREAdvocacySummit #GGSummit23 #SanDiego #RAREDisease

200 people with 200 unique stories. Zeal Access can make sure those stories get told and shared.

Enzyme replacement therapy (ERT) is a treatment that replaces the missing or deficient GAA enzyme, helping to break down glycogen and prevent muscle damage. #PompeDisease #RareDisease #PompeDay

International #Pompe Day is April 15. Having #PompeDisease doesn’t make you different. We’re all different! Shared by the Pompe community and brought to life by inspired artists. You can share your own experiences and wisdom by using the tag #PompePearls. #PompeDay #RareDisease

This #FabryAwarenessMonth, we’re sharing stories from women living with #FabryDisease to raise awareness of the impact it can have on mental well-being. For Christy, a lack of awareness and understanding of the disease led to feelings of self-doubt.

Baseball legend Bernie Williams, formerly of the New York Yankee (and currently a jazz musician), discusses his advocacy work to raise awareness of interstitial lung diseases, including idiopathic pulmonary fibrosis #IPF #checkrare @boehringerus checkrare.com/bernie-william…

Happy #RareDiseaseDay2023 from the Zeal Access Team! #raredisease

When you put it in real life context, how rare is rare anyway? #RareDisease #RareDiseaseDay #Pompe #PompeDisease

“By 2030, it is estimated that at least 30 non-oncology gene therapies will be approved in the United States alone. These therapies could be used to treat up to 50,000 patients annually & have the potential to result in major shifts in disease management.” pubmed.ncbi.nlm.nih.gov/36681872/

Nobody Has My Condition But Me newyorker.com/magazine/2023/… via @NewYorker and @beverlygage

@TheWantonWench This is how much we give to charities

The Rare Disease Rallying Cry: If Not Me, Who? | The power of self-advocacy. Article by @kathleen_bogart psychologytoday.com/ca/blog/disabi…

Zion Clark (@bigz97), wrestler without legs, wins professional MMA fight bloodyelbow.com/2022/12/20/235…

If you need a few laughs, check out this thread

Celine Dion suffering from Moersch-Woltman syndrome, won't resume world tour montreal.ctvnews.ca/celine-dion-su…

An oldie but a goodie by @EndangeredComic

A neat sight on today’s dog walk. #DisabilityRights #DisabilityHistoryMonth CC: Sign in front of church that reads: “Dignity rights & wellbeing for persons with disabilities.”