NSGC 2019 Conference Highlights Part 1
Genetic Counselors are an incredible resource – they can help assess your risk of developing a condition, the risk of your children inheriting a condition,
- Rare Disease News
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Usher 1F Collaborative
Usher 1F Collaborative
Usher 1F Collaborative is a U.S. nonprofit foundation whose mission is to fund medical research to save or restore the vision of those with Usher Syndrome type 1F. When we began in 2013, there was no research specific to Usher 1F. Since then, patients and families working together with scientists have brought about the development of gene, drug, and stem cell therapies at eight research labs around the world. If you or a family member has Usher 1F, please join us in our work to find a cure. Visit our website at https://www.usher1f.org and email us at info@usher1f.org
Condition Awareness & Advocacy
Here is a list of conditions this partner raises awareness and advocacy for:
Patient Worthy Posts on Usher Syndrome
ProQR And The Use of RNA Therapies for Rare Genetic Disorders
In a story for Drug Development & Delivery, the CEO of the biotechnology company ProQR, Daniel de Boer, recently sat down for an interview. In
Family Takes Action After Facing Usher Syndrome
According to a story from newton.wickedlocal.com, the first time that mother Melissa Chaikof realized that something was wrong with her oldest doctor was many years
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Doctors Are Unable to Diagnose Many Rare Diseases. Genome Sequencing is Changing That Scenario
After twenty-two years physician Huang Chun-jung finally learned why his vision and hearing have fallen to thirty percent of normalcy, thanks to research conducted by
LEGO to Introduce Braille Bricks for Children who are Blind! Coming to Stores in 2020
The Importance of Braille For any child with a rare disease that leads to blindness or visual impairment such as Stargardt disease, Usher Syndrome, Alström
