PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
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.
Sleep disorders with PSP
These sleep disorders can be caused by the underlying neurodegenerative process of PSP, as well as by medications used to manage PSP symptoms.
Sleep disorders with PSP
These sleep disorders can be caused by the underlying neurodegenerative process of PSP, as well as by medications used to manage PSP symptoms.
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.