Atypical Parkinsonism Blog

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Atypical Parkinsonism Blog by: Laura Louizos

UTI's in Progressive Supranuclear Palsy PSP

UTIs with PSP

Laura Louizos

UTIs with PSP can become tricky fast!

UTIs with PSP

Laura Louizos

UTIs with PSP can become tricky fast!

Sleep wake regulation in Neurodegenerative DIseases (PSP, MSA, CBD)

Sleep wake regulation in PSP

Laura Louizos

Sleep/wake regulation that can lead to profound sleep deprivation

Sleep wake regulation in PSP

Laura Louizos

Sleep/wake regulation that can lead to profound sleep deprivation

PSP Genetics

Does PSP run in families?

Laura Louizos

Short answer; It is very uncommon but not impossible.Ā 

Does PSP run in families?

Laura Louizos

Short answer; It is very uncommon but not impossible.Ā 

PSP Progressive Supranuclear Palsy Eye Issues

What are some Eye issues with PSP?

Laura Louizos

We hear a lot of questions about eye issues in PSP (Progressive Supranuclear Palsy). This might help!

3 comments

What are some Eye issues with PSP?

Laura Louizos

We hear a lot of questions about eye issues in PSP (Progressive Supranuclear Palsy). This might help!

3 comments
U Step Walker for Atypical Parkinsonism

U Step Walker! Could it be a game changer?

Laura Louizos

The U-Step 2 Walking Stabilizer was designed to increase independence andĀ decreaseĀ falling among those with neurological conditions.

U Step Walker! Could it be a game changer?

Laura Louizos

The U-Step 2 Walking Stabilizer was designed to increase independence andĀ decreaseĀ falling among those with neurological conditions.

What are the 4 Stages for PSP?

What are the 4 Stages for PSP?

Laura Louizos

It has been said there are four stages, but because there is so little research they are a guideline only.

111 comments

What are the 4 Stages for PSP?

Laura Louizos

It has been said there are four stages, but because there is so little research they are a guideline only.

111 comments

Laura Louizos, Blog Author

Laura Louizos is a blogger an 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 shared her personal journey as a caregiver, including her struggles, triumphs, and insights. She now provides resources and information about the disease, as well as tips and advice for living with PSP and other neurodegenerative diseases. Laura's writing is candid, inspiring, and informative, and her blog has become an important resource for the community worldwide.

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.