Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
Join us in Backing UHN's Rossy PSP Centre in th...
As a dedicated Canadian federal non-profit corporation, our mission at Coleen Cunningham Foundation for PSP Awareness is not just to raise awareness about PSP but to actively support individuals and...
Join us in Backing UHN's Rossy PSP Centre in th...
As a dedicated Canadian federal non-profit corporation, our mission at Coleen Cunningham Foundation for PSP Awareness is not just to raise awareness about PSP but to actively support individuals and...
Specialized Hospice Care for Progressive Supran...
This condition, characterized by significant motor function difficulties, balance problems, and cognitive impairment, escalates with time, eventually necessitating full-time care. It's here, in the latter stages of the disease, that...
Specialized Hospice Care for Progressive Supran...
This condition, characterized by significant motor function difficulties, balance problems, and cognitive impairment, escalates with time, eventually necessitating full-time care. It's here, in the latter stages of the disease, that...
Zoom Support Group Meetings
Zoom Support Group Meetings every Thursday 7-9pm starting June 29, 2023
Zoom Support Group Meetings
Zoom Support Group Meetings every Thursday 7-9pm starting June 29, 2023
Enhancing Mobility and Independence: The U-Step...
This innovative assistive device offers numerous benefits, allowing individuals to regain mobility, confidence, and a sense of freedom.
Enhancing Mobility and Independence: The U-Step...
This innovative assistive device offers numerous benefits, allowing individuals to regain mobility, confidence, and a sense of freedom.
Cherishing Each Day: Embracing Life with a PSP ...
Life is an extraordinary gift, and it is often during our most challenging moments that we come to truly appreciate its value.
Cherishing Each Day: Embracing Life with a PSP ...
Life is an extraordinary gift, and it is often during our most challenging moments that we come to truly appreciate its value.
Laura Louizos, Blog Author
Laura Louizos is a blogger an 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 shared her personal journey as a caregiver, including her struggles, triumphs, and insights. She now provides resources and information about the disease, as well as tips and advice for living with PSP and other neurodegenerative diseases. Laura's writing is candid, inspiring, and informative, and her blog has become an important resource for the community worldwide.
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.