PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
AlphaLift Mobility Lifter: A Game-Changer for P...
Living with Progressive Supranuclear Palsy (PSP) presents numerous challenges, affecting one's mobility and independence. Among the many difficulties PSP patients face, transportation can be particularly daunting. Traditional mobility solutions like...
AlphaLift Mobility Lifter: A Game-Changer for P...
Living with Progressive Supranuclear Palsy (PSP) presents numerous challenges, affecting one's mobility and independence. Among the many difficulties PSP patients face, transportation can be particularly daunting. Traditional mobility solutions like...
Alleviating Symptoms: The Off-Label Use of Oral...
Using atropine drops orally to manage excessive secretions, including phlegm and saliva, is an off-label but often effective practice, especially in conditions like Progressive Supranuclear Palsy (PSP). PSP is a...
Alleviating Symptoms: The Off-Label Use of Oral...
Using atropine drops orally to manage excessive secretions, including phlegm and saliva, is an off-label but often effective practice, especially in conditions like Progressive Supranuclear Palsy (PSP). PSP is a...
Navigating Clinical Trials for Progressive Supr...
Navigating clinical trials for Progressive Supranuclear Palsy (PSP) can be a complex process, but online platforms like ClinicalTrials.gov provide an accessible avenue. Clinical trials are research studies aiming to evaluate...
Navigating Clinical Trials for Progressive Supr...
Navigating clinical trials for Progressive Supranuclear Palsy (PSP) can be a complex process, but online platforms like ClinicalTrials.gov provide an accessible avenue. Clinical trials are research studies aiming to evaluate...
Illuminating the Path: Red Light Therapy for Ne...
In a world filled with numerous treatments and therapies, some methods rise above others through their uniqueness and promising results. One such method is Red Light Therapy (RLT). This therapy...
Illuminating the Path: Red Light Therapy for Ne...
In a world filled with numerous treatments and therapies, some methods rise above others through their uniqueness and promising results. One such method is Red Light Therapy (RLT). This therapy...
Progressive Supranuclear Palsy: Medications and...
This blog post will delve into the medications currently used to manage PSP and highlight some promising clinical trials that offer hope for the future.
Progressive Supranuclear Palsy: Medications and...
This blog post will delve into the medications currently used to manage PSP and highlight some promising clinical trials that offer hope for the future.
Utilizing CBD Oil and THC for Managing PSP Symp...
Tthe emerging potential of cannabinoids, particularly Cannabidiol (CBD) and Delta-9-Tetrahydrocannabinol (THC), in managing symptoms and possibly slowing the progression of neurodegenerative diseases like PSP has generated a buzz in the...
Utilizing CBD Oil and THC for Managing PSP Symp...
Tthe emerging potential of cannabinoids, particularly Cannabidiol (CBD) and Delta-9-Tetrahydrocannabinol (THC), in managing symptoms and possibly slowing the progression of neurodegenerative diseases like PSP has generated a buzz in the...
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.