Deans' stroke musings: Demand Support for Parkinson’s Research

Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Thursday, March 8, 2018

Demand Support for Parkinson’s Research

Look at what can occur when a disease foundation has a strategy and the leadership to followup that strategy. Our fucking failures of stroke associations can't even copy successful non-profits, they are that fucking bad. And our boards of directors don't seem to know how bad they are.
60,000 Americans are diagnosed with Parkinson's disease each year as compared to 800,000 strokes in the USA. Which disease needs more help?
http://view.michaeljfox-email.org/?qs=a65221134ee9840df0039ef42be0e899a1dcf00021cf2374aee7d34ddce3c202dc5f18fb2768a4deae9b8cc2b329657281c571096146bedc69d9514a5cb35f298a8ed05344eb23fe3ffd1affc228cc56

Dear Friend,

Over the next few days, a bipartisan group of U.S. representatives is taking action to support Parkinson's disease (PD) research. It's crucial that we join these efforts and speak up for the PD community.

These lawmakers are circulating letters asking their colleagues in the House of Representatives to fund a national Parkinson's disease database and two agencies that conduct PD research. This is an important step in the process to obtain critically needed funding!

It's important to act now as there are only a few days left to secure signatures. Your representative has until March 14 to join the letters. The more signatures they receive, the more likely it is that the database and research programs will be funded. Urge your legislator to sign on now!