PSP BLOG

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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018

Global Atypical Parkinsonism Awareness Walk MAY 2024

Global Atypical Parkinsonism Awareness Walk MAY...

Join the Global Atypical Parkinsonism Awareness Walk MAY 2024! Calling all change-makers and advocates! We are thrilled to announce the Global Atypical Parkinsonism Awareness Walk 2024, taking place in May...

Global Atypical Parkinsonism Awareness Walk MAY...

Join the Global Atypical Parkinsonism Awareness Walk MAY 2024! Calling all change-makers and advocates! We are thrilled to announce the Global Atypical Parkinsonism Awareness Walk 2024, taking place in May...

Thursday Zoom Support Group: On The Journey - Supports and Resources

Thursday Zoom Support Group: On The Journey - S...

Join Our Weekly Thursday Zoom Support Group: On The Journey - Supports and Resources We are excited to extend an invitation to our weekly support group meeting, β€œOn The Journey...

Thursday Zoom Support Group: On The Journey - S...

Join Our Weekly Thursday Zoom Support Group: On The Journey - Supports and Resources We are excited to extend an invitation to our weekly support group meeting, β€œOn The Journey...

Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders.

Atypical Parkinsonism Awareness Pack designed t...

Get Yours Today on Amazon! Introducing the Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders. This pack includes: - 4 unique Teal Awareness Vinyl Decals:...

Atypical Parkinsonism Awareness Pack designed t...

Get Yours Today on Amazon! Introducing the Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders. This pack includes: - 4 unique Teal Awareness Vinyl Decals:...

Rare Disease Day: Shining a Light on Progressive Supranuclear Palsy (PSP)

Rare Disease Day: Shining a Light on Progressiv...

Today, on Rare Disease Day, we turn our focus towards a condition that many may not have heard of, yet it profoundly impacts the lives of those it touches: Progressive...

Rare Disease Day: Shining a Light on Progressiv...

Today, on Rare Disease Day, we turn our focus towards a condition that many may not have heard of, yet it profoundly impacts the lives of those it touches: Progressive...

Tim Talks Session #3

Tim Talks Session #3

Join us tonight on Zoom for an enlightening session of Tim Talks, where our guest speaker, Tim, will share his journey and insights as a 9-year warrior battling Progressive Supranuclear...

Tim Talks Session #3

Join us tonight on Zoom for an enlightening session of Tim Talks, where our guest speaker, Tim, will share his journey and insights as a 9-year warrior battling Progressive Supranuclear...

Little Caesars Fundraiser PICK UP Update

Little Caesars Fundraiser PICK UP Update

First and foremost, I want to extend a heartfelt thank you to everyone who participated in our Little Caesars fundraiser. Your enthusiasm and support have been incredible, and we are...

Little Caesars Fundraiser PICK UP Update

First and foremost, I want to extend a heartfelt thank you to everyone who participated in our Little Caesars fundraiser. Your enthusiasm and support have been incredible, and we are...

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.