PSP BLOG
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Progressive Supranuclear Palsy PSP Blog by Laura Louizos, Since 2018
Why does it take so long to get a diagnosis for...
PSP, MSA, CBD is a clinical diagnosis and can only be officially confirmed after an autopsy. This makes it hard along with how rare and little is known about them to...
Why does it take so long to get a diagnosis for...
PSP, MSA, CBD is a clinical diagnosis and can only be officially confirmed after an autopsy. This makes it hard along with how rare and little is known about them to...
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.
Does it matter PSP, CBD, MSA?
It does matter for research purposes and to try and better understand these diseases.
Does it matter PSP, CBD, MSA?
It does matter for research purposes and to try and better understand these diseases.
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
U Step Walker! Could it be a game changer?
The U-Step 2 Walking Stabilizer was designed to increase independence and decrease falling among those with neurological conditions.
U Step Walker! Could it be a game changer?
The U-Step 2 Walking Stabilizer was designed to increase independence and decrease falling among those with neurological conditions.
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.