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.

Friday, June 24, 2022

FDA releases 5-year action plan to combat neurodegenerative diseases

Because we have fucking failures of stroke associations  we are getting nothing to help the hundreds of thousands of yearly stroke survivors in the US.

FDA releases 5-year action plan to combat neurodegenerative diseases

The FDA on June 23 announced a 5-year strategy for improving and extending the lives of people with rare neurodegenerative diseases by advancing development of safe and effective medical products and facilitating access to novel treatments.

The plan, which will serve as a blueprint for how the agency will move forward in tackling challenges in drug development, was developed in accordance with the Accelerating Access to Critical Therapies for ALS Act that President Joe Biden signed into law in December 2021, the FDA said in a press release.

Source: Adobe Stock.
Source: Adobe Stock.

“The effects of rare neurodegenerative diseases are devastating, with very few effective therapeutic options available to patients,” FDA Commissioner Robert M. Califf, MD, said in the release. “We recognize the urgent need for new treatments that can both improve and extend the lives of people diagnosed with these diseases.”

According to the release, during the 5-year span, the plan will focus on bolstering scientific advancement and promoting innovation by:

  • establishing the FDA Rare Neurogenerative Disease Task Force;
  • establishing the public-private partnership for rare neurodegenerative diseases;
  • developing disease-specific science strategies; and
  • leveraging ongoing FDA regulatory science efforts.

A key focus of the plan is the ALS Science Strategy, which provides a forward-learning framework for FDA activities to assess key regulatory science priorities. Highlights of the strategy include:

  • improving characterization of disease pathogenesis and natural history;
  • facilitating patient access to new drugs whenever possible and promoting greater participation in clinical trials by reducing barriers and burdens faced by minority populations; and
  • enhancing clinical trial infrastructure and agility to enable early selection of promising therapeutic candidates for further development, optimizing clinical trial design, improving access to the trials, streamlining trail operations and reducing the time and cost of drug development.

Per the release, success of the FDA’s implementation of the ALS Science Strategy will rely on patient engagement, public workshop, research projects and collaboration with the NIH.

“To face that challenge and to accelerate drug development, we need innovative approaches to better understand these diseases while also building on current scientific and research capabilities,” Califf said. “This action plan, especially including the use of public-private partnerships and direct involvement of patients, will ensure the FDA is working toward meeting the task set forth by Congress to enhance the quality of life for those suffering by facilitating access to new therapies.”

 

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