PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
Red Light Therapy and PSP
RLT works by stimulating the production of ATP (adenosine triphosphate) in cells, which can help improve cellular function and reduce inflammation. This may have benefits for PSP, as inflammation is...
Red Light Therapy and PSP
RLT works by stimulating the production of ATP (adenosine triphosphate) in cells, which can help improve cellular function and reduce inflammation. This may have benefits for PSP, as inflammation is...
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...
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...
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...
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...
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...
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...
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...
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.