Lori Verton’s Post

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President ACMCRN | Leading Rare Disease Research in Arachnoiditis

So many thousands of patient-volunteers and their allies have spent years of full time, unpaid work in effort to try to find treatments and support for their #raredisease communities, with little to no assistance from government or the private sector. Why is society leaving it up to the sick to find their own treatments and support millions of suffering patients, while corporations like big oil and big pharma still get handed subsidies despite already being successful? It's well past time that similar investments are made by governments and big pharma into non-profits who do the actual work of serving patient communities. Investments provided to rare disease non-profits saves healthcare/ mental health costs down the line and any new findings echo for generations thereafter. Hey big business peeps! What's your excuse for not giving? Most organizations run only on private peer to peer fundraising donations. What does it say that most of our funding in the past 3 years have been bequeaths and being named "charity of choice" from our members who have passed, living out their lives to the end with no real treatment for their #raredisease? We need our communities to do better! Please help! #Arachnoiditis

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