PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
Dementia and PSP “Like Dementia, But Not Dementia”
By: Laura Louizos My mom would mix up her days sometimes and call people to reschedule thinking she was late or double book. Planning becomes an issue as the brain...
Dementia and PSP “Like Dementia, But Not Dementia”
By: Laura Louizos My mom would mix up her days sometimes and call people to reschedule thinking she was late or double book. Planning becomes an issue as the brain...
Moving, Stairs, Falls & Atypical Parkinsonism
If possible to always have someone nearby, seems to be the best prevention of falls.
Moving, Stairs, Falls & Atypical Parkinsonism
If possible to always have someone nearby, seems to be the best prevention of falls.
How do you gauge the progression and timeline w...
It’s so tough to gauge. Can somethings make it worse?
How do you gauge the progression and timeline w...
It’s so tough to gauge. Can somethings make it worse?
UTIs with PSP
UTIs with PSP can become tricky fast!
UTIs with PSP
UTIs with PSP can become tricky fast!
Sleep wake regulation in PSP
Sleep/wake regulation that can lead to profound sleep deprivation
Sleep wake regulation in PSP
Sleep/wake regulation that can lead to profound sleep deprivation
What are some Eye issues with PSP?
We hear a lot of questions about eye issues in PSP (Progressive Supranuclear Palsy). This might help!
What are some Eye issues with PSP?
We hear a lot of questions about eye issues in PSP (Progressive Supranuclear Palsy). This might help!
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.