RT @LivingLFS
Thank you Senator @JerryMoran and staff of the great state of Kansas for speaking to Living LFS representative Lon Humpert at #RareDC2023 about #LiFraumeniSyndrome during #LFSawarenessMonth @EveryLifeOrg @RareAdvocates
#raredc2023 #lifraumenisyndrome #lfsawarenessmonth
Nearly 100% of women with Li-Fraumeni syndrome (LFS) and 75% of men with LFS get cancer in their lifetimes. Check us out at Charity Navigator and Guidestar before you donate: 100% of us at Living LFS are volunteers, so 100% of your dollars directly help those with LFS who are in need. Thank you for supporting our mission 💙 https://livinglfs.org/donate
#GivingTuesday #GivingTuesday2022 #cancer #lifraumenisyndrome #lifraumeni #genetics #livinglfs
#givingtuesday #givingtuesday2022 #cancer #lifraumenisyndrome #lifraumeni #genetics #livinglfs
Howdy! I'm the volunteer VP of Living LFS, a #nonprofit supporting those with #LiFraumeniSyndrome #cancer. For money I produce the Your Money, Your Wealth #podcast. I'm #progressive #bisexual married, into #photography #art #music #science #nature #podcasting #politics #climatechange #humanrights #equality. I mostly lurked on the birdsite and would rather find #community here. Nice to meetcha. 3am in #SanDiego, why not do an #introduction ?
#nonprofit #lifraumenisyndrome #cancer #podcast #progressive #bisexual #photography #art #music #science #nature #podcasting #politics #climatechange #humanrights #equality #community #sandiego #introduction