Nonprofit Founder and Executive Director. Rare epilepsy advocate. Funding ๐งฌ gene therapy research through HopeforULD.org
ULD (EPM1) is Unverricht-Lundborg Disease, a rare, genetic, Progressive Myoclonic Epilepsy. It is an autosomal recessive disease.
๐ rare epilepsy advocate
๐ rare disease advocate ๐ฆ
๐ mental health advocate
๐ disability advocate ๐จ๐ฝโ๐ฆฝ
๐ grateful for Jesus Christ โ๏ธ
๐ grateful for family & friends
๐ animals are blessings ๐ถ
๐ kindness matters
๐ฌ๐ง ๐ฑ๐ป๐โ๏ธ๐Curious about neuroscience, tech, AI, new places to explore
๐ Former teacher and reporter; lifelong learner
โค๏ธ๐งถโ๏ธ๐ท๐งณ๐๐จโ๐ฉโ๐งโ๐ฆ๐ชด๐บ๐ถ๐๐โ๏ธ
I am here to learn, engage, share ideas!
Invited by: Tamarine Mullenaux
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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% |