Atypical Parkinsonism Blog

Many New Blog Posts Each Week

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Atypical Parkinsonism Blog by: Laura Louizos

Lighting Up Burlington Pier for PSP Awareness: A Beacon of Hope

Lighting Up Burlington Pier for PSP Awareness: ...

Laura Louizos

On May 30th, from 8 PM to midnight, the Burlington Pier will be bathed in a radiant teal glow. This illuminating event is more than just a beautiful spectacle; it’s...

Lighting Up Burlington Pier for PSP Awareness: ...

Laura Louizos

On May 30th, from 8 PM to midnight, the Burlington Pier will be bathed in a radiant teal glow. This illuminating event is more than just a beautiful spectacle; it’s...

Ice Cream Challenge

Ice Cream Challenge

Laura Louizos

Atypical Parkinsonism Ice Cream Challenge for PSP, MSA, CBD and DLB PSP- Progressive Supranuclear Palsy MSA- Multiple System Atrophy CBD- Corticobasal Degeneration DLB- Dementia with Lewy Bodies  May is Awareness...

Ice Cream Challenge

Laura Louizos

Atypical Parkinsonism Ice Cream Challenge for PSP, MSA, CBD and DLB PSP- Progressive Supranuclear Palsy MSA- Multiple System Atrophy CBD- Corticobasal Degeneration DLB- Dementia with Lewy Bodies  May is Awareness...

🌟 You’re Invited to Tim Talks! 🌟

🌟 You’re Invited to Tim Talks! 🌟

Laura Louizos

Join us this Thursday, April 25th, from 7-9 PM ET for an inspiring session with PSP Warrior, Tim Brown! This month, we’re diving into awareness topics to gear up for...

🌟 You’re Invited to Tim Talks! 🌟

Laura Louizos

Join us this Thursday, April 25th, from 7-9 PM ET for an inspiring session with PSP Warrior, Tim Brown! This month, we’re diving into awareness topics to gear up for...

Happy National Volunteer Week!

Happy National Volunteer Week!

Laura Louizos

As we celebrate this special week, we want to extend a heartfelt thank you to all our dedicated volunteers. Your selfless contributions and unwavering commitment have been instrumental in making...

Happy National Volunteer Week!

Laura Louizos

As we celebrate this special week, we want to extend a heartfelt thank you to all our dedicated volunteers. Your selfless contributions and unwavering commitment have been instrumental in making...

Support & Advocacy Committee

Support & Advocacy Committee

Laura Louizos

Join us in supporting and raising awareness for those affected by Atypical Parkinsonism, including PSP, MSA, CBD, and DLB.We're thrilled to introduce our new Support & Advocacy Committee!Keep an eye...

Support & Advocacy Committee

Laura Louizos

Join us in supporting and raising awareness for those affected by Atypical Parkinsonism, including PSP, MSA, CBD, and DLB.We're thrilled to introduce our new Support & Advocacy Committee!Keep an eye...

CurePSP Awareness Month Kit, MAY 2024

CurePSP Awareness Month Kit, MAY 2024

Laura Louizos

Don't miss your opportunity to make a real difference this May! Equip yourself with all the necessary tools to raise awareness for PSP, CBD and MSA. Our May Month of...

CurePSP Awareness Month Kit, MAY 2024

Laura Louizos

Don't miss your opportunity to make a real difference this May! Equip yourself with all the necessary tools to raise awareness for PSP, CBD and MSA. Our May Month of...

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.