FD Foundation is the leader in FD treatment and research.
Our mission is to raise funds & operate programs with best medical treatment & sci. research for FD
Tonight, we will be honoring
#BenRainer
. His friends from all over the multi-verse will gather and pay tribute.
Tune live here 8:00 PM EDT
Throughout the night, we will be raising money for
@famdys
in Ben's name, at the link below:
As we commemorate 70 years of serving the FD community, we acknowledge that only because of friends like you we have been able to accomplish so much.
We sincerely thank you for your continuous interest & support.
#jumpforfd
#jewish
#boxjumpchallenge
#ashkenazi
#nervoussystem
Thank you to everyone who joined us for
#FDDay2021
! Didn't catch the live program? Keep an eye out for videos of this year's event in the coming weeks. We look forward to seeing you next year at the 37th annual FD Day!
Caregivers Brian and Stephanie Stillman recently shared why they fundraise for
#FDMatch19
: "We fundraise to support Pyper, in the hopes of a cure, and to give her a chance at a full life."
Support patients like Pyper:
Here is a SNEAK PEAK painting by Mara Clawson, one of five artists who will be exhibiting at TEARLESS on April 7th! Mara titled this piece "Pancake Love"
Reserve your tickets or become a sponsor here!
Such a pleasure to have Dr. Lefcort speak during
#FDday2022
.
Frances Lefcort is a Research Professor at Montana State University and her lab studies the molecular, cellular, and systems-wide mechanisms that cause the clinical symptoms of FD.
#RareDisease
#jewish
#art
#FDday
We are excited for this year’s FD Day to kick-off in 1 hour at 11AM EST. Throughout the event, you will hear from our expert panel of intl physicians & researchers. It’s not too late to register for the virtual event! For more information go to
#FDDay2020
Join comedian
@EliLebowicz
on 12/6 as he hosts UNIFIED, an exciting virtual concert benefitting the FD Foundation. Register at for a fun filled afternoon of music, & don’t forget to invite your friends via the Facebook event below!
Thank you to the Dysautonomia Center team members
@nyulangone
for supporting the
#JumpforFD
#BoxJumpChallenge
😍 💜 💖
Today, we nominate all of YOU to join the fun, jump on board and post your video!
Today kicks off Jewish Disability Awareness & Inclusion Month (JDAIM)! Join us as we enhance visibility 4 FD starting w the JCC Chicago Film Festival’s viewing & talkback of Living Art (film avail. now, disc. 2/3) & culminating w Rare Disease Day. How r u raising awareness 4 FD?
Rare Disease Day fact 2 FD is classified as a rare disease because there r less than 350 individuals living w/ this genetic disorder worldwide. That is why we work to enhance awareness on this day, & throughout the year. What r u doing to increase awareness for Rare Disease Day?
Check out our latest FD Heroes comic, featuring Lindsay R.!
Last call for people who’d like to be featured as an FD Hero IRL. Please let us know if you’d like to participate, as the series is coming to an end.
#famdys
#familialdysautonomia
#fd
#raredisease
#featurefriday
Did you know it’s Jewish Genetic Screening Awareness Week? FD 1 of the rarest of genetic disorders can be tested for by
@MyJScreen
Use the coupon for a discount on genetic testing. Don’t forget to share it with friends to raise awareness about FD & how easy it is to
#getscreened
!
February is Jewish Disability Awareness, Acceptance & Inclusion Month! Join the FD Foundation, JCC Chicago & Sarnoff Center 2/3/2021 for a free virtual screening & talkback about “Living Art,” a film by David Rochkind feat. Mara Clawson an artist with FD.
Today’s FD community lives all over the world, & many r cared 4 by local physicians. NYU’s Dysautonomia Center has provided a list of articles that u can share with ur local doctors & nurses 2 help increase their understanding of FD. View the resources:
Have you registered for FD Day 2021 yet? For the 2nd year you’ll be able to enjoy presentations from experts in FD from the comfort of your home! Register for FD Day, support the event and/or participate in the opening video “I’m/We’re Watching From…" at
Have you been following the
#BoxJumpChallenge
?
Thanks to all the generous donors we have raised $30,000 so far! 👏 & thanks to all the jumps we have raised awareness for FD 🥳
Today we invite you to join the
#BoxJumpChallenge
and
#jumpforfd
Donate at:
We're excited for this year's FD Day kicking off in 1 hour at 11am EDT. Throughout the event, you will hear from our expert panel of international physicians & researchers. It's not too late to register for the virtual event! For more information go to
Have you donated yet to support your sibling, child, cousin, friend with FD? Donate today to support medical care and research at NYU's Dysautonomia Center!
So....what are you waiting for?
Register today for this amazing course! "Demystifying Entrepreneurship For Youth with Disabilities"
The purpose of this
#course
is to break down barriers to entrepreneurship for
#youth
with self-identified
#disabilities
and/or
#mentalhealth
conditions.
Are you interested in learning more about
#planned
giving?
Join Forever Devoted today!
Simply include language in your will/trust specifying that a gift be made to
@FamDys
as part of your estate plan.
To learn more contact us at 212.279.1066; info
@famdys
.org
#makeawillmonth
.
@TheJewishMuseum
: Access Family Workshop
Visitors with intellectual or developmental
#disabilities
and their families are invited to explore the
#exhibition
May 28, 2023
10:30 am – 4 pm ET
All Access Prog are free of charge & require reservation
Recently, our very own Keshi Taryan-Kigel participated in a virtual production of Shakespeare’s Twelfth Night. Keshi contributed her personal artwork & acting talents as the priest/servant. Mazel tov Keshi on a wonderful performance! View the performance
Taking advantage of Amazon Prime deals today? You can support the FD Foundation while you shop! It’s easy!
-Go to
-Choose the Dysautonomia Foundation, Inc.
-Shop!
A portion of your purchases will benefit the Foundation & those living w/ FD
FD Foundation works for the benefit of all people afflicted with FD, by supporting medical care and scientific research, as well as conducting social service and public awareness programs.
To learn more visit
#jewish
#ashkenazi
#autonomic
#raredisease
For Rare Disease Day, the Foundation will be sharing facts to enhance awareness about familial dysautonomia. Fact 1: Approximately 1 in 30 Ashkenazi Jews are carriers for FD
How are you showing your stripes today? Let us know in the comments below!