Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
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.
Urinary incontinence with PSP
Urinary incontinence is the involuntary loss of urine, which can range from occasional leaking to a complete loss of bladder control.
Urinary incontinence with PSP
Urinary incontinence is the involuntary loss of urine, which can range from occasional leaking to a complete loss of bladder control.
Caregiving and PSP
It's important for caregivers to recognize that caring for someone with PSP can be a long-term and challenging journey.
Caregiving and PSP
It's important for caregivers to recognize that caring for someone with PSP can be a long-term and challenging journey.
Laura Louizos, Blog Author
Laura Louizos is a blogger, advocate, and founder of the Coleen Cunningham Foundation (CCF), raising awareness for atypical Parkinsonism, including PSP. Inspired by her mother’s 2018 PSP diagnosis, Laura shares her caregiver journey—struggles, triumphs, and insights—while offering resources and tips for living with neurodegenerative diseases. Her candid, inspiring blog supports a global community. Passionate and dedicated, Laura amplifies understanding and hope for those affected.
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