Colorado man hits roadblock to try experimental ALS drug, "Just give me an opportunity"
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Grateful for another Thanksgiving, an ALS patient reflects on living with terminal disease
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Life changed drastically when ALS hit, just as Covid had already upended our social world. That first year was isolating—nights spent on the porch, questioning everything. But from that struggle, we found unexpected strength and closeness. Our family, #thejeansonne7, grew into a force of love, proving that beauty can rise from the ashes. love. #OnwardForward #brianjeansonne #Blove414 #thejeansonne7 #theJ7 #ALSawareness #LivingWithALS #ALSsupport #MotorNeuronDisease #LouGehrigsDisease #ALS
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How I remember finding out my dad was diagnosed with ALS, a terminal illness. Something was taken from me that wasn't supposed to be taken? - Jonah #BrianJeansonne #thejeansonne7 #ALSawareness #ALS #lougehrigsdiseasesucks
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Kaitlin Gonzales has been living with ALS for 9 years—and recently joined Her ALS Story and ALS TDI during our ALS Town Hall series to shed light on the lesser-known symptoms of ALS that often go unspoken. From acid tears to chronic pain that’s too often overlooked, Kaitlin bravely shared how these symptoms have shaped her experience—and why open conversations like this matter so much. This powerful discussion is part of our ongoing Town Hall series, hosted by Her ALS Story and ALS TDI, aimed at
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Bryan talks about his first encounter with #ALS on our recent #podcast …
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