Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
CORD presents Rare Disease Drug Strategy Webinars
PMPRB: Friend or Foe of Rare Disease Drug Strategy In February 2019 the federal government committed $1billion over two years starting in 2022 to set up a Canadian Rare Disease...
CORD presents Rare Disease Drug Strategy Webinars
PMPRB: Friend or Foe of Rare Disease Drug Strategy In February 2019 the federal government committed $1billion over two years starting in 2022 to set up a Canadian Rare Disease...
RETROTOPE UPDATE RT001 Drug Trial
US FDA Allows Trial to Proceed for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP).LOS ALTOS, CALIF, April 25, 2020– Retrotope announced today that it received a “Study...
RETROTOPE UPDATE RT001 Drug Trial
US FDA Allows Trial to Proceed for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP).LOS ALTOS, CALIF, April 25, 2020– Retrotope announced today that it received a “Study...
Association of Stress-Related Disorders
Association of Stress-Related Disorders With Subsequent Neurodegenerative Diseases By: Huan Song, MD, PhD; Johanna Sieurin, MSc; Karin Wirdefeldt, MD, PhD Original Investigation | March 9, 2020 Key Points Question Do...
Association of Stress-Related Disorders
Association of Stress-Related Disorders With Subsequent Neurodegenerative Diseases By: Huan Song, MD, PhD; Johanna Sieurin, MSc; Karin Wirdefeldt, MD, PhD Original Investigation | March 9, 2020 Key Points Question Do...
Clinical trials RT001 for PSP-UPDATE
RETROTOPE UPDATE! I will be meeting with the RETROTOPE team tomorrow March 5th in California and will provide an update shortly after. In the interim here is an update from Sarah...
Clinical trials RT001 for PSP-UPDATE
RETROTOPE UPDATE! I will be meeting with the RETROTOPE team tomorrow March 5th in California and will provide an update shortly after. In the interim here is an update from Sarah...
UPDATE on RT001 Clinical Trials for PSP
From Sarah at Retrotope regarding RT001 Clinical Trials for PSP! Do not lose hope. Retrotope is in the process of developing drugs to treat a variety of neurological diseases, and...
UPDATE on RT001 Clinical Trials for PSP
From Sarah at Retrotope regarding RT001 Clinical Trials for PSP! Do not lose hope. Retrotope is in the process of developing drugs to treat a variety of neurological diseases, and...
The Falls and Frustrations of PSP
Written by Matthew J. Barrett, an associate professor of neurology and a movement disorder specialist at Virginia Commonwealth University in Richmond, Virginia. I often repeat her presentation to medical students: my...
The Falls and Frustrations of PSP
Written by Matthew J. Barrett, an associate professor of neurology and a movement disorder specialist at Virginia Commonwealth University in Richmond, Virginia. I often repeat her presentation to medical students: my...
Laura Louizos, Blog Author
Laura Louizos is a blogger, advocate, and founder of the Coleen Cunningham Foundation (CCF), raising awareness for atypical Parkinsonism, including PSP. Inspired by her mother’s 2018 PSP diagnosis, Laura shares her caregiver journey—struggles, triumphs, and insights—while offering resources and tips for living with neurodegenerative diseases. Her candid, inspiring blog supports a global community. Passionate and dedicated, Laura amplifies understanding and hope for those affected.
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