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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018

Clinical Trials Investigating Potential Treatments for PSP

Clinical Trials Investigating Potential Treatme...

Progressive supranuclear palsy (PSP) is a rare and progressive neurodegenerative disorder for which there is currently no cure. However, there are ongoing clinical trials investigating potential treatments for PSP. These...

1 comment

Clinical Trials Investigating Potential Treatme...

Progressive supranuclear palsy (PSP) is a rare and progressive neurodegenerative disorder for which there is currently no cure. However, there are ongoing clinical trials investigating potential treatments for PSP. These...

1 comment
Red Light Therapy Testimonial for use with PSP

Red Light Therapy Testimonial for use with PSP

Fitz’s Story Originally Posted on Well Red David Fitzgerald was a teacher, orator, nurseryman, cricket fanatic, bush-walker, traveler and IT-guru. He was a larger-than-life character with a wicked sense of...

9 comments

Red Light Therapy Testimonial for use with PSP

Fitz’s Story Originally Posted on Well Red David Fitzgerald was a teacher, orator, nurseryman, cricket fanatic, bush-walker, traveler and IT-guru. He was a larger-than-life character with a wicked sense of...

9 comments
Red light therapy (RLT) for PSP, MSA, CBD, Atypical Parkinsonism

Red Light Therapy (RLT) with PSP, MSA, CBD

Red light therapy (RLT) is a treatment that may help skin, muscle tissue, and other parts of your body heal. It exposes you to low levels of red or near-infrared...

3 comments

Red Light Therapy (RLT) with PSP, MSA, CBD

Red light therapy (RLT) is a treatment that may help skin, muscle tissue, and other parts of your body heal. It exposes you to low levels of red or near-infrared...

3 comments
Treatment of Disturbed Sleep in PSP

Treatment of Disturbed Sleep in PSP

FEATURED STUDY: Treatment of Disturbed Sleep in PSP The Treatment of Disturbed Sleep in persons with Progressive Supranuclear Palsy (PSP) is a remote, six-week clinical trial sponsored by the University...

Treatment of Disturbed Sleep in PSP

FEATURED STUDY: Treatment of Disturbed Sleep in PSP The Treatment of Disturbed Sleep in persons with Progressive Supranuclear Palsy (PSP) is a remote, six-week clinical trial sponsored by the University...

Four electrodes placed in brain of patient with PSP disease

Mumbai doctors perform rare brain surgery in PSP

Four electrodes placed in brain of patient with PSP syndrome during six-hour-long procedure. In a first, doctors at Mumbai’s Jaslok Hospital recently performed a deep brain simulation (DBS) surgery by...

1 comment

Mumbai doctors perform rare brain surgery in PSP

Four electrodes placed in brain of patient with PSP syndrome during six-hour-long procedure. In a first, doctors at Mumbai’s Jaslok Hospital recently performed a deep brain simulation (DBS) surgery by...

1 comment
RETROTOPE UPDATE RT001 Drug Trial

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...

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.