PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
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...
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...
US FDA Grants Orphan Drug Designation for RT001
US FDA Grants Orphan Drug Designation for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP). LOS ALTOS, CALIF, February 18, 2020– Retrotope announced today that the U.S. Food...
US FDA Grants Orphan Drug Designation for RT001
US FDA Grants Orphan Drug Designation for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP). LOS ALTOS, CALIF, February 18, 2020– Retrotope announced today that the U.S. Food...
Laura Louizos, Blog Author
Laura Louizos is a blogger and advocate for PSP (Progressive Supranuclear Palsy) and Founder of CCF for PSP Awareness.
PSP is a rare and debilitating neurological disorder that affects movement, balance, vision, speech, and cognitive function. Laura's mother was diagnosed with PSP in 2018, and since then, Laura has been dedicated to raising awareness about the disease and providing support to others affected by it.
Through our blog, Laura shares her personal journey as a caregiver, including her struggles, triumphs, and insights. She also provides resources and information about the disease, as well as tips and advice for living with PSP. Laura's writing is candid, inspiring, and informative, and her blog has become an important resource for the PSP community.
Laura is a passionate advocate for PSP awareness, and she works tirelessly to increase understanding and support for those affected by the disease. Her blog is a testament to her dedication and commitment to improving the lives of those with PSP, and she is a valuable voice in the fight against this devastating condition.