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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018

Advance Directives & Their Importance in Progressive Supranuclear Palsy (PSP)

Advance Directives & Their Importance in Progre...

PSP, or Progressive Supranuclear Palsy, is a fast-progressing neurodegenerative disease. With its symptoms often impairing communication abilities, it can introduce many challenges for patients and their families. Hence, the importance...

Advance Directives & Their Importance in Progre...

PSP, or Progressive Supranuclear Palsy, is a fast-progressing neurodegenerative disease. With its symptoms often impairing communication abilities, it can introduce many challenges for patients and their families. Hence, the importance...

Caregivers guide to psp

A Guide for Family Caregivers of Loved Ones New...

Progressive supranuclear palsy (PSP) is a rare brain disorder that causes serious and progressive problems with gait and balance, as well as complex eye movement and thinking problems. Being a...

1 comment

A Guide for Family Caregivers of Loved Ones New...

Progressive supranuclear palsy (PSP) is a rare brain disorder that causes serious and progressive problems with gait and balance, as well as complex eye movement and thinking problems. Being a...

1 comment
The Integral PSP Care Team: Understanding Their Roles in Managing Progressive Supranuclear Palsy

The Integral PSP Care Team: Understanding Their...

Managing Progressive Supranuclear Palsy (PSP) involves a multidisciplinary team to address the broad range of symptoms and challenges the patient may face. The care team often includes:1. Neurologist: Typically leads...

1 comment

The Integral PSP Care Team: Understanding Their...

Managing Progressive Supranuclear Palsy (PSP) involves a multidisciplinary team to address the broad range of symptoms and challenges the patient may face. The care team often includes:1. Neurologist: Typically leads...

1 comment
Unveiling the Role of the MoCA Test in Identifying Progressive Supranuclear Palsy

Unveiling the Role of the MoCA Test in Identify...

In the realm of cognitive and neurological assessment, the Montreal Cognitive Assessment (MoCA) has emerged as a critical tool for diagnosing various conditions, including Progressive Supranuclear Palsy (PSP). PSP is...

Unveiling the Role of the MoCA Test in Identify...

In the realm of cognitive and neurological assessment, the Montreal Cognitive Assessment (MoCA) has emerged as a critical tool for diagnosing various conditions, including Progressive Supranuclear Palsy (PSP). PSP is...

Rocket Chair and PSP: A Deeper Dive into Progressive Supranuclear Palsy Care

Rocket Chair and PSP: A Deeper Dive into Progre...

The intricate worlds of neurology and daily caregiving often collide in unique and unexpected ways, particularly when we delve into the topics of Progressive Supranuclear Palsy (PSP) and a behavior...

3 comments

Rocket Chair and PSP: A Deeper Dive into Progre...

The intricate worlds of neurology and daily caregiving often collide in unique and unexpected ways, particularly when we delve into the topics of Progressive Supranuclear Palsy (PSP) and a behavior...

3 comments
Broadening Horizons: Sharing PSP Awareness Beyond Our Inner Circles

Broadening Horizons: Sharing PSP Awareness Beyo...

Every day, individuals, families, and medical professionals grapple with the impact of Progressive Supranuclear Palsy (PSP), a neurodegenerative disease that remains under-recognized both in the public sphere and within many...

Broadening Horizons: Sharing PSP Awareness Beyo...

Every day, individuals, families, and medical professionals grapple with the impact of Progressive Supranuclear Palsy (PSP), a neurodegenerative disease that remains under-recognized both in the public sphere and within many...

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.