#curesforall search results
Children don’t get brain tumors because of God. They get them because society funds war over cures, greed over healing, and profit over people. Don’t blame the Light — blame the darkness we chose. open.substack.com/pub/iholdtheto… #Genesis13 #FaithAndTruth #CuresForAll #LetThereBeLight…
Genesis 1:3 on Rockin’ Robin’s Mockery and the Truth About Suffering “And God said, Let there be light: and there was light.” — Genesis 1:3 Light doesn’t shy away from the hard questions. It illuminates them. Today someone mocked faith with this: “As I live and breathe, a…
Longevity is a debate, but cures aren’t. People deserve to live healthy, pain-free lives. Let’s focus on unlocking cures that improve quality of life and bring balance—not disruption—to humanity. #CuresForAll #QualityOfLife #EthicalInnovation”
When a stage in life leaves you in limbo...#advocate #raredisease #curesforall #addisonsdisease #caregiver Check out my blog post wix.to/7amrXh7 #newblogpost
As we approach Rare Disease Day! 10,000 rare diseases affecting over 300 million worldwide. In the U.S. 1 in 10 at least half children. One number that hasn't grown is 5% of rare diseases w/ cures. #IGaveBirthToMyHero #rarediseaseday2024 #curesforall advocatelikeararemother.com/post/rare-dise…
advocatelikeararemother.com
Rare Disease Day Facts
Every year on this last day of February we, in the rare disease world, celebrate Rare Disease Day. Why on the last Day of February, you ask? Because it is the rarest day of the year every four years,...
New blog post - trying to keep this active with Rare Disease Day coming next week!! #igavebirthtomyhero #rarediseaseday #curesforall #addisonsdisease #caretaker #mentalhealth #adrenalinsufficiency advocatelikeararemother.com/post/life-thro…
advocatelikeararemother.com
Life Through a Different Lens - The Rare Perspective
I can remember being a new mom, back more than 22 years ago and worrying about every little thing that happened or may happen. I can remember laying in bed at night and wondering if I was enough, if...
#raredisease #curesforall #advocacy #addisons #ftd #mentalhealth advocatelikeararemother.com/post/i-don-t-k…
As our nation celebrates its independence, AFTD looks forward to the day when we can celebrate a world #FreeOfFTD ❤️ 🏢 AFTD will be closed today, and we will resume normal operations on Wednesday, July 5th.
I count my blessings through the tears in this post. #FTD #dementia #curesforall #raredisease #showyourstripes #patientsrisingnow #advocacy #EveryFTDStoryCounts #formydaddy #advocatelikeadaughter advocatelikeararemother.com/post/missing-d…
advocatelikeararemother.com
Missing Dad While He is Still "Here"
Let me start this off by saying I know that I am blessed that I still have my dad in my life. That is not something I take for granted for a second. Over five years ago my dad was diagnosed with...
As mom to 2 young men with rare medical conditions I want men to find places for support, education and advocacy. #curesforall #addisons #igavebirthtomyheroes #adrenalinsufficiency #raredisease #chronicillness #advocacy #MentalHealthAwareness advocatelikeararemother.com/post/where-are…
advocatelikeararemother.com
Where are all the Men? Rare Disease Edition
In one of our forums recently a man asked if the illness he had was more common in men or if it was just that men were more likely to seek our advice and support. As the mother of two young adult men...
We are fighting to change the world for the entire ALS community! Special thanks to @iamalsorg and everyone who braved the rain in Times Square today to raise awareness for ALS! #CuresforAll #OurALSCommunity
I will change the world for @hilliard_jim #Curesforall #StrikeOutALS #Iamals @TeamHilliardALS @iamalsorg
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