Some of the provisions include:
*accelerated development of breakthrough therapies that show early promise
*Faster Access to Specialized Treatments (FAST)
*Transforming the Regulatory Environment to Accelerate Access to Treatments (TREAT act)
*enhanced FDA consultation with rare disease medical experts
I have attached some links of organizations whose objectives are to advocate for rare diseases, assist in the development of treatments, help patients, and collaborate with regulatory agencies in various capacity for rare disease patients. Please refer to the links as I find them very helpful.
http://kakkis.org/
The EveryLife Foundation for Rare Diseases is dedicated to accelerating biotech innovation for rare disease treatments through science-driven public policy. We can do more with the science we already have and bring life-saving treatments to millions of people suffering from rare diseases.
http://www.advocacyforpatients.org/
WELCOME to Advocacy for
Patients with Chronic Illness...
Patients with Chronic Illness...
Where patients can get free information, advice and advocacy services in areas including but not limited to the following:
• | How to get your own medical records. | ||
• | How to get and keep health insurance. | ||
• | How to get health insurance coverage for particular treatments, drugs, and/or therapies. | ||
http://mymuscleteam.lotsahelpinghands.com/caregiving/home/ “What can I do to help?” MDA welcomes you to myMuscleTeam®. We are proud to offer this free personal community and care coordination service. http://www.thespeakfoundation.com/pages/ Welcome The Speak Foundation is a non-profit organization dedicated to helping people overcome the challenges of physical disability or a serious health condition, by providing social support, advocacy, and financial assistance both in the United States and internationally (e.g. sponsorship of orphans with disabilities). You can read more about our mission here. | |||
2 comments:
Amazing woman
Thank you, I appreciate your feedback.
Tara
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