Nonprofit Founder and Executive Director. Rare epilepsy advocate. Funding 🧬 gene therapy research through HopeforULD.org
ULD (EPM1) is Unverricht-Lundborg Disease, a rare, genetic, Progressive Myoclonic Epilepsy. It is an autosomal recessive disease.
💜 rare epilepsy advocate
💜 rare disease advocate 🦠
💜 mental health advocate
💜 disability advocate 👨🏽🦽
💜 grateful for Jesus Christ ✝️
💜 grateful for family & friends
💜 animals are blessings 🐶
💜 kindness matters
🔬🧠📱💻🚙✈️🏖Curious about neuroscience, tech, AI, new places to explore
📖 Former teacher and reporter; lifelong learner
❤️🧶☕️🍷🧳📚👨👩👧👦🪴🌺🎶🚙🏖✈️
I am here to learn, engage, share ideas!
Invited by: Tamarine Mullenaux
if the data has not been changed, no new rows will appear.
Day | Followers | Gain | % Gain |
---|---|---|---|
August 15, 2023 | 202 | +12 | +6.4% |
November 18, 2022 | 190 | +3 | +1.7% |
September 09, 2022 | 187 | +12 | +6.9% |
July 29, 2022 | 175 | +2 | +1.2% |
July 07, 2022 | 173 | +4 | +2.4% |
May 30, 2022 | 169 | +3 | +1.9% |
April 23, 2022 | 166 | +3 | +1.9% |
March 19, 2022 | 163 | +13 | +8.7% |
January 21, 2022 | 150 | +8 | +5.7% |
December 14, 2021 | 142 | +20 | +16.4% |