The CGDAA is committed to advocating on behalf of patients and X-linked carriers by providing news and information about Chronic Granulomatous Disease.
Proud to partner w top research-scientists at @NIH & #PIDTC to co-author a study on X-linked female carriers of #CGD, which was just published in the top, peer-reviewed medical journal for #Immunology@ClinImmSoc
Read more about it in @CGDAofAmerica
https://t.co/yi4opoiLIZ
Look forward to seeing everyone at the @IDFCommunity conference for this special dinner, hosted by @CGDAofAmerica! RSVP at info @ https://t.co/PiIgzE2Da0.
Join us for CGD Association of America’s Zoom Meeting with Crystal Cruz to discuss her son’s inspiring & innovative transplant journey, tomorrow, June 11th at 8 PM EST. Email us for the Zoom invitation at [email protected]
https://t.co/pJYHzPt2Qb
Excited to attend @IDFCommunity’s PI Conference in Chicago 6/20-6/22 to learn the latest in #immunology & #gene therapy from the world’s leading experts, such as this key session w/ Dr. Malech, Chief of Genetic Immunotherapy, @NIH
& moderated by Felicia Morton
@CGDAofAmerica
Presenting @CGDAofAmerica’s latest news& research @ the Primary Immune Deficiency Treatment Consortium, hosted by @EmoryUniversity in Atlanta; honored to be sharing our success helping PI patients w/ the 200+ top #immunologists across North America who help make it possible!
Thanks to all who came out to the J.McLaughlin event to support the @CGDAofAmerica. It was super fun & great to see everyone. Let’s continue to work together to raise awareness for #CGD and advance research!
Join Us in Chicago this Summer for @IDFCommunity PI Conference June 20 - 22, 2024
Scholarships for #CGD Patients & Families Available. Deadline is today! To register:
https://t.co/juyMXJaqt7
@Info4PI@CGDSociety
@SCIDAngels
@HyperIgM
Honored to be featured in Bold Journey Magazine; thanks to @lizziecarlile & @VoyageLAmag for the opportunity to show what women w/ a passion for making a difference in #raredisease can accomplish!
https://t.co/ZfDWgErwZ7
@remember_girls@Info4PI
@SCIDAngels
@angelaidcares
Join Brittany Hinman 12/5 @ 8 pm EST to learn about life after her son’s successful BMT & how she turned her trials w CGD into talent as a photographer. Email us at [email protected] for the Zoom invitation. All are welcome!
@CGDSociety@remember_girls@IDFCommunity@HyperIgM
Today is #GivingTuesday2023 and at the @CGDAofAmerica, we are stronger because of you! Take a look at what we’ve accomplished together, and with your support, we’ll continue to make a difference for #CGD: https://t.co/vrFvTOpkyd
#Immunologists: You're invited to participate in a survey by #UNC to help understand the #genetics resources you use, including #ClinGen, an #NIH -funded initiative that aims to improve precision medicine and research. https://t.co/9qVEcYZ722
It's a wrap! Heading back home after another productive experience at @GlobalGenes#Rare Disease Summit in San Diego. Many thanks to @HorizonNews for sponsoring this "rare opportunity" for nonprofit leaders in this space to come together, learn, grow, and get inspired!
Join us tomorrow on Zoom for this important talk to delve into what physicians look for in an annual exam after #CGD patients have recovered from #BMT. Email us at [email protected] for the link.
Honored to just do an interview on @DNATodayPodcast, People's Choice award winner & voted best #science & #medicine podcast in '20, '21, & '22. It was an important opportunity to talk about @CGDAofAmerica & the advancements in #genetic testing. Stay tuned for air date!