PSP BLOG
Many New Blog Posts Every Week
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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...
End of Year Meeting with Cookie Exchange!
Dear Members, As the year draws to a close, we’re excited to invite you to our last in person support group meeting of 2023, scheduled for November 27th at Port...
End of Year Meeting with Cookie Exchange!
Dear Members, As the year draws to a close, we’re excited to invite you to our last in person support group meeting of 2023, scheduled for November 27th at Port...
The Awareness Shop: Making a Difference with Ev...
The Awareness Shop is more than just a store; it's a movement dedicated to raising awareness and supporting those affected by Progressive Supranuclear Palsy, Multiple System Atrophy, and Corticobasal Degeneration This shop...
The Awareness Shop: Making a Difference with Ev...
The Awareness Shop is more than just a store; it's a movement dedicated to raising awareness and supporting those affected by Progressive Supranuclear Palsy, Multiple System Atrophy, and Corticobasal Degeneration This shop...
Giving Tuesday Offer: Support a Great Cause and...
This holiday season, we’re excited to offer a special gift for our generous donors. For every donation made until Christmas, you’ll receive a unique Awareness Ribbon as a token of...
Giving Tuesday Offer: Support a Great Cause and...
This holiday season, we’re excited to offer a special gift for our generous donors. For every donation made until Christmas, you’ll receive a unique Awareness Ribbon as a token of...
Join Our Awareness Campaign at Burlington Mall ...
Are you looking for a meaningful way to contribute to your community this holiday season? We have an exciting opportunity for you! On December 14th, we are hosting an awareness...
Join Our Awareness Campaign at Burlington Mall ...
Are you looking for a meaningful way to contribute to your community this holiday season? We have an exciting opportunity for you! On December 14th, we are hosting an awareness...
🌟 Volunteer with Us! 🌟
Looking to make an impact? Our foundation is on the lookout for passionate volunteers! Dive into diverse projects, meet like-minded changemakers, and bring joy to those in need. Your journey...
🌟 Volunteer with Us! 🌟
Looking to make an impact? Our foundation is on the lookout for passionate volunteers! Dive into diverse projects, meet like-minded changemakers, and bring joy to those in need. Your journey...
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.