Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
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.
Advanced Planning with PSP
Here are some advanced planning considerations for individuals with PSP and their families.
Advanced Planning with PSP
Here are some advanced planning considerations for individuals with PSP and their families.
PSP Trials
Clinical trials are an important way to advance our understanding of the disease and develop new treatments.
PSP Trials
Clinical trials are an important way to advance our understanding of the disease and develop new treatments.
Medications for PSP Symptoms
The medications used for PSP typically target the specific symptoms of the disease.
Medications for PSP Symptoms
The medications used for PSP typically target the specific symptoms of the disease.
Marijuana and PSP
Some studies have suggested that medical marijuana may be beneficial for managing certain symptoms of PSP, such as pain, muscle stiffness, and sleep disturbances.
Marijuana and PSP
Some studies have suggested that medical marijuana may be beneficial for managing certain symptoms of PSP, such as pain, muscle stiffness, and sleep disturbances.
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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