Lupus Foundation of America has been doing walk fundraisers for more than 8 years now, and this year, I was fortunate enough to be in New York City to take part and be able to raise some money in finding a cure for lupus.
“The Lupus Foundation of America is the only national force devoted to solving the mystery of lupus, one of the world’s cruelest, most unpredictable and devastating diseases, while giving caring support to those who suffer from its brutal impact. Through a comprehensive program of research, education, and advocacy, we lead the fight to improve the quality of life for all people affected by lupus.”
They have walkers from almost sixty cities across the USA who have raised money and joined this event. Some of them are lupus patients, some are family members of those with the disease, and others are caregivers or medical professionals who take care of patients with SLE (Systemic Lupus Erythemathosus).
Four days before the event, I began my fundraising post on facebook. With just a few days left before the walk, with the help of family and friends, we were able to raise $375!!!
Thank yous go out to these awesome people:
My husband Marco
My parents Dith & Ed
Sibs- Kyt & Mack, and Kim & Chris
Relatives- Tita Mikki & Tito Joshua, and Greta Goetz & family
And friends- Nins Cortez, George & Kathy Luttrell, Kina & Phil Poggiali, Jo Ann & Joe Piper, Tita Malou Latonio, and Nins & Patrick Jimenez
The foundation was able to raise a total of $409,426, is that amazing or what?! Their goal was to raise $565,000, and they were able to reach 72% of their target.
May 14, 2016, 8:30 AM, registration started for the “Walk to End Lupus Now” event at the South Street Seaport in New York City.
Can you image how great it would be when they finally find a cure, and I can get pregnant without my antibodies attacking my baby in my tummy?! Because of your help, and all the donations that the foundation received, we are one step closer to that cure. And if not for my generation, then for the next.
MAY is lupus awareness month, and YOU can help. Ask a friend you are having dinner with if they know what lupus is, tell a co-worker, help spread awareness. Ignorance is not an excuse, understanding and compassion comes with being well informed. Together, let us spread lupus awareness. As Tracy Chapman said, “If not now then when?”
Edited by: Kylie Padilla