Atypical Parkinsonism Blog

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Atypical Parkinsonism Blog by: Laura Louizos

International Caregivers Day

International Caregivers Day

Laura Louizos

Happy International Caregivers Day to all the incredible members of our community! Today, we celebrate each one of you - the unsung heroes who dedicate your days and nights, your...

International Caregivers Day

Laura Louizos

Happy International Caregivers Day to all the incredible members of our community! Today, we celebrate each one of you - the unsung heroes who dedicate your days and nights, your...

Happy Easter

Happy Easter

Laura Louizos

As we embrace the vibrant hues of Spring and the joyful spirit of Easter, we want to extend our warmest wishes to each and every one of you. This season,...

1 comment

Happy Easter

Laura Louizos

As we embrace the vibrant hues of Spring and the joyful spirit of Easter, we want to extend our warmest wishes to each and every one of you. This season,...

1 comment
Global Atypical Parkinsonism Awareness Walk MAY 2024

Global Atypical Parkinsonism Awareness Walk MAY...

Laura Louizos

Join the Global Atypical Parkinsonism Awareness Walk MAY 2024! Calling all change-makers and advocates! We are thrilled to announce the Global Atypical Parkinsonism Awareness Walk 2024, taking place in May...

Global Atypical Parkinsonism Awareness Walk MAY...

Laura Louizos

Join the Global Atypical Parkinsonism Awareness Walk MAY 2024! Calling all change-makers and advocates! We are thrilled to announce the Global Atypical Parkinsonism Awareness Walk 2024, taking place in May...

Thursday Zoom Support Group: On The Journey - Supports and Resources

Thursday Zoom Support Group: On The Journey - S...

Laura Louizos

Join Our Weekly Thursday Zoom Support Group: On The Journey - Supports and Resources We are excited to extend an invitation to our weekly support group meeting, β€œOn The Journey...

Thursday Zoom Support Group: On The Journey - S...

Laura Louizos

Join Our Weekly Thursday Zoom Support Group: On The Journey - Supports and Resources We are excited to extend an invitation to our weekly support group meeting, β€œOn The Journey...

Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders.

Atypical Parkinsonism Awareness Pack designed t...

Laura Louizos

Get Yours Today on Amazon! Introducing the Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders. This pack includes: - 4 unique Teal Awareness Vinyl Decals:...

Atypical Parkinsonism Awareness Pack designed t...

Laura Louizos

Get Yours Today on Amazon! Introducing the Atypical Parkinsonism Awareness Pack designed to support and educate on atypical Parkinsonian disorders. This pack includes: - 4 unique Teal Awareness Vinyl Decals:...

Rare Disease Day: Shining a Light on Progressive Supranuclear Palsy (PSP)

Rare Disease Day: Shining a Light on Progressiv...

Laura Louizos

Today, on Rare Disease Day, we turn our focus towards a condition that many may not have heard of, yet it profoundly impacts the lives of those it touches: Progressive...

Rare Disease Day: Shining a Light on Progressiv...

Laura Louizos

Today, on Rare Disease Day, we turn our focus towards a condition that many may not have heard of, yet it profoundly impacts the lives of those it touches: Progressive...

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.