Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
Assistive Devices & Adaptive Equipment List By:...
CurePSP has collected the following suggestions for assistive devices and adaptive equipment from patients and families experiencing neurodegenerative diseases.
Assistive Devices & Adaptive Equipment List By:...
CurePSP has collected the following suggestions for assistive devices and adaptive equipment from patients and families experiencing neurodegenerative diseases.
PSP Awareness Walk Canada
PSP Awareness Walk on Saturday, June 3rd 2023, at the beautiful Confederation Beach Park. Ontario, Canada
PSP Awareness Walk Canada
PSP Awareness Walk on Saturday, June 3rd 2023, at the beautiful Confederation Beach Park. Ontario, Canada
Dementia, Executive Function and PSP
While not all individuals with PSP will develop dementia, studies have shown that up to 80% of individuals with PSP may experience some degree of cognitive impairment.
Dementia, Executive Function and PSP
While not all individuals with PSP will develop dementia, studies have shown that up to 80% of individuals with PSP may experience some degree of cognitive impairment.
MAID Canada
In Canada, medical assistance in dying (MAID) is legal for individuals who meet certain eligibility criteria.
MAID Canada
In Canada, medical assistance in dying (MAID) is legal for individuals who meet certain eligibility criteria.
Canada Supports for PSP
It can be helpful to do some research and connect with local organizations or support groups to find additional resources and support in your area.
Canada Supports for PSP
It can be helpful to do some research and connect with local organizations or support groups to find additional resources and support in your area.
Communication Strategies for PSP
There are strategies and tools that can help individuals with PSP communicate more effectively.
Communication Strategies for PSP
There are strategies and tools that can help individuals with PSP communicate more effectively.
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.