22q11 syndromes APPG. This is not an official feed of the House of Commons or the House of Lords. It has not been approved by either House or its committees.
Meet Kelly du Plessis: Founder and CEO.
She founded RDSA after the diagnosis of her son with #Pompe.
She is responsible for keeping the organization on track, & to ensure all those who are impacted have improved quality of life.
#Care4Rare#AwareAboutRare#LivingBeyond
The new year is a great time to start, or continue, to raise awareness for 22q11 syndrome and show our support for those affected. #togetherwearestronger
Only a few hours remain to make a donation in 2017...
With the International 22q11.2 Foundation in your corner, we are “STRONGER TOGETHER!" Please click here to read our year end message & give today: https://t.co/wiL8DOGRvU #22q
First learning about 22q11.2 deletion or duplication can be overwhelming - hear from parents about managing the diagnosis, taking the next steps and how to live and thrive with 22q! Watch video here - https://t.co/flbii1OTgx #MyChildHas22q#22qawareness
Just in time for the Holiday Season, the 2018 Faces of Sunshine Calendar is here! It is a beautiful way to bring in the New Year, while showing your 22q pride and support. Click here for more info: https://t.co/14FNXHClsi
https://t.co/2a0SX1GARR
Treatable Immune System Disorder Could Be Mistaken For Schizophrenia or Bipolar Disorder
~Results will be used to develop more sensitive tests aiding detection of attacking antibodies
https://t.co/ivpWHLh0rQ
Indiv with #22q11DS have immune deficiencies & 1:4 develop schizophrenia
Attention 22q Moms!!! The 22q Family Foundation Moms Retreat tickets are on sale NOW!! Join us and fellow moms, grandmas and caretakers from around the country (and elsewhere) for a weekend of relaxation, fun, and stress free living.
https://t.co/v16EUsRLXH