PSP BLOG

Many New Blog Posts Every Week

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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018

The Butcherbird Sings By: Julie Campbell

The Butcherbird Sings By: Julie Campbell

What do you do when a neurodegenerative disease slowly robs your husband of his mind and dignity and all that he treasures in life?How do your children cope in the...

The Butcherbird Sings By: Julie Campbell

What do you do when a neurodegenerative disease slowly robs your husband of his mind and dignity and all that he treasures in life?How do your children cope in the...

Progressive Supranuclear Palsy Medical Resource Journal for Patients, Caregivers and Doctors.

Progressive Supranuclear Palsy PSP Medical Reso...

Included in the customized 400 page PSP resource journal; * Information on Progressive Supranuclear Palsy including symptoms, quick facts and a disease outline * Personal Information page with emergency contacts*...

Progressive Supranuclear Palsy PSP Medical Reso...

Included in the customized 400 page PSP resource journal; * Information on Progressive Supranuclear Palsy including symptoms, quick facts and a disease outline * Personal Information page with emergency contacts*...

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.