PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
The Power of Shared Experience: PSP Caregivers ...
The journey as a caregiver for someone with progressive supranuclear palsy (PSP) is one that is often filled with unique challenges, yet it also provides us with a unique bond....
The Power of Shared Experience: PSP Caregivers ...
The journey as a caregiver for someone with progressive supranuclear palsy (PSP) is one that is often filled with unique challenges, yet it also provides us with a unique bond....
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 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...
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...
Importance of Hospice and Palliative Care for I...
Progressive Supranuclear Palsy (PSP) is a complex and rapidly progressive condition that presents unique challenges for both individuals and their caregivers. In such difficult times, the importance of hospice and...
Importance of Hospice and Palliative Care for I...
Progressive Supranuclear Palsy (PSP) is a complex and rapidly progressive condition that presents unique challenges for both individuals and their caregivers. In such difficult times, the importance of hospice and...
The Inference between Primary Progressive Aphas...
Primary Progressive Aphasia (PPA) and Progressive Supranuclear Palsy (PSP) are two distinct neurological disorders. Understanding the nuances between the two can aid in appropriate diagnoses and subsequently, more effective treatment...
The Inference between Primary Progressive Aphas...
Primary Progressive Aphasia (PPA) and Progressive Supranuclear Palsy (PSP) are two distinct neurological disorders. Understanding the nuances between the two can aid in appropriate diagnoses and subsequently, more effective treatment...
Some of our services we offer to our community
📣 We are thrilled to share the range of services we offer to our community at no charge!1️⃣ Respite Care Grants: We understand the vital role of respite in maintaining...
Some of our services we offer to our community
📣 We are thrilled to share the range of services we offer to our community at no charge!1️⃣ Respite Care Grants: We understand the vital role of respite in maintaining...
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.