PSP BLOG

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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018

Tim Talks Session #3

Tim Talks Session #3

Laura Louizos

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

Laura Louizos

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

Laura Louizos

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

Laura Louizos

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...

Caregiver Support After the Journey - Grief and Loss

Caregiver Support After the Journey - Grief and...

Laura Louizos

Join us for a compassionate and informative Zoom support meeting, "Caregiver Support After the Journey - Grief and Loss." This virtual gathering is designed to provide a safe and understanding...

Caregiver Support After the Journey - Grief and...

Laura Louizos

Join us for a compassionate and informative Zoom support meeting, "Caregiver Support After the Journey - Grief and Loss." This virtual gathering is designed to provide a safe and understanding...

We’re Back and Ready for an Exciting 2024!

We’re Back and Ready for an Exciting 2024!

Laura Louizos

Hello Everyone,We’re thrilled to announce that we are resuming our work tomorrow, January 8th, after a much-needed holiday break. These past weeks have been challenging personally, as I battled COVID...

We’re Back and Ready for an Exciting 2024!

Laura Louizos

Hello Everyone,We’re thrilled to announce that we are resuming our work tomorrow, January 8th, after a much-needed holiday break. These past weeks have been challenging personally, as I battled COVID...

Atypical Parkinsonism: Navigating the Unknown and Embracing What's Known

Atypical Parkinsonism: Navigating the Unknown a...

Laura Louizos

Atypical Parkinsonism is a group of neurological disorders that share some symptoms with Parkinson's disease but differ in certain key aspects, including their progression and response to treatment. For individuals...

Atypical Parkinsonism: Navigating the Unknown a...

Laura Louizos

Atypical Parkinsonism is a group of neurological disorders that share some symptoms with Parkinson's disease but differ in certain key aspects, including their progression and response to treatment. For individuals...

Tim Talks - November 30th, 7-9 PM Eastern Time

Tim Talks - November 30th, 7-9 PM Eastern Time

Laura Louizos

Join us for an inspiring evening with our special guest, Tim Brown – a passionate PSP warrior! 🔹 First Hour: Dive into a Q&A session with Tim, where he’ll share his...

Tim Talks - November 30th, 7-9 PM Eastern Time

Laura Louizos

Join us for an inspiring evening with our special guest, Tim Brown – a passionate PSP warrior! 🔹 First Hour: Dive into a Q&A session with Tim, where he’ll share his...

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.