Ran into Thee Coach Carter at the new Richmond Farmers Market. We talked about his experiance with Moringa in Senegal where the tree is called Nebadye (Never Die) because of its hardiness and ability to maintain growth during drought and other harsh conditions. If you dont know who coach carter is, google him, he is almost as popular as Moringa.

September 21st, 2024 Suisun, Ca Sickle Cell Event Delta Sigma Theta

Working in the local community , engaging and educating youth on the benefits of Moringa's cultivation and consumption.

NW Sickle Cell and North of England Thalassaemia & RIA HCC present a 1-hour education session Presentation: Nutrition in Sickle Cell Presenter: Claudine Matthews, MSC, Registered Dietician Date: 22/08/22 Please note this video is aimed at health care professionals for training purposes rather than the general public.

Heading to Mississippi to drop off a couple Kilos of Moringa powder, I think I have enough fresh Moringa leaves to last for the trip, what you think? Stay tuned!

This session features Christen Brown, a community leader, social scientist and entrepreneur. He is the Creative Director of Creation Of Society, and his work has been to connect community needs to community-controlled solutions in the forms of, but not limited to, rites of passage, product quality control, educational workshops, entrepreneurship trainings and skill development seminars. This is a recorded session of where Christen talks about nutrition content for Sickle Cell patients. ----------------------------------------------------------------------------------------------------------------------- ABOUT: The 2023 Advocacy and Empowerment Program Course Training is a program for the sickle cell community inspired by Sickle Cell Anemia Awareness of San Francisco, non-profit. This program spans over 9 months of the year, with one 1-2 hour meeting sessions every month. It is led by experienced sickle anemia disease medical professionals and patient community leaders who are working to broaden awareness and improve healthcare for sickle cell patients. For more information about our organization and resources, visit: https://www.scaasf.org/ For information about our 2023 Advocacy and Empowerment program and list of speakers, visit: https://www.scaasf.org/advocacy-and-empowermentt

This is a nine minute segment into a ongoing series of solutions for the sickle cell community to minimize the invasive approach brought about by western medicine.

Blessed to be rocking out with my first born for BLACK history month. Its a mystery how we got the shortest month of the year but we keeping vibrations high 365.