Hello my name is Gabrielle Mason. If you know me personally then you know I’m a mother of four beautiful girls one who has a special needs disability. Her name is Da’Miyah Mason and she was diagnosed with a rare genetic disorder called Angelman Syndrome. I’ve started a fundraiser for my baby in hopes for a cure and The foundation the funds will be going to is the fast foundation. This foundation is stating that they can have a cure for my daughters disease within the next 10 years but they need help with funding. I don’t know if you all have heard of this rare disorder but because it’s so rare they have a hard time finding support for this charity. Angelman Syndrome takes so much from my daughter and I really need your support even if it’s 5$ anything will help. We have a goal of 500$ that we hope to accomplish by the end of the year. I’ve also started a retail business selling youth girls clothes sizes 2t to 14/16, mommy and me items, jewelry and accessories. My online store will be open to public may of 2023 and we will be donating 3% of our profits to this foundation. As our business grows so will that percentage. We hope to reach our  overall goal of 10%. Please follow my business page on Facebook @gsangelgalleria and instagram @gsangelgalleria for all the latest updates on this cause. My 9 year old life is filled with doctors appointments, physical occupational, and speech therapy. The disorder takes her speech causing her to be mute. It causes her to suffer from epilepsy disorder and insomnia. Overall they are extremely happy individuals despite everything they go through which is the bright side of the disorder. Please don’t hesitate to ask me more questions and make a friendly donation towards my cause. Thank you for your support. 

Better Days Are Coming! Together we CAN cure Angelman syndrome.FAST researchers know exactly what causes Angelman syndrome (AS) and have already cured it in the laboratory. Much of this pioneering, critical research was funded by our FAST community. Today, this research has led to the announcement of several revolutionary clinical trials that hold the potential to treat, and ultimately cure this rare disorder.Please help me support this critical research that CAN make a significant difference in the life of my loved one living with AS by clicking the Give Now button and donating whatever you CAN. Every amount is appreciated and gets us closer to our goal! The more people that know about FAST, the greater the impact, so please spread the word by sharing this page.Your donation to my page will help fund critical research to accelerate the therapeutic pipeline that will benefit all individuals living with AS, regardless of age or genotype. Thank you in advance for your generosity!