I sent this letter to my senator. I encourage everyone to speak up. We can’t sit back and just watch.
Sent this to Senator Mark Kelly today.
Thank you for everything you and Gabby have done for our country.
I write you now because The Multiple Sclerosis Research Program, better known as MSRP was denied funding for Fiscal Year 2025. Another brilliant decision…NOT. I have primary progressive MS. About 15% of people with MS are diagnosed with PPMS. MS is not like other diseases because it affects everyone differently…there is no known direction this disease will go for anyone and at my age - 68, there is no treatment…and now, no hope.
BTW, how much money is being spent on legal proceedings to prevent this government takeover to dictatorship? We don’t know what direction our country is going in, anymore than we know what direction MS is going in.