Atypical Parkinsonism Blog

Many New Blog Posts Each Week

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Atypical Parkinsonism Blog by: Laura Louizos

LegalZoom's Estate Plan Bundle

LegalZoom's Estate Plan Bundle

Laura Louizos

LegalZoom offers a comprehensive estate plan bundle. It includes a will, living trust, and power of attorney. Easy online process with attorney support. Affordable and customizable plans. Purchasing through our...

LegalZoom's Estate Plan Bundle

Laura Louizos

LegalZoom offers a comprehensive estate plan bundle. It includes a will, living trust, and power of attorney. Easy online process with attorney support. Affordable and customizable plans. Purchasing through our...

DR-HO'S Pain Therapy System Pro

DR-HO'S Pain Therapy System Pro

Laura Louizos

DR-HO'S Pain Therapy System Pro is a versatile device for pain relief. It uses TENS, EMS, and AMP to target and alleviate pain. Easy to use with customizable settings for...

DR-HO'S Pain Therapy System Pro

Laura Louizos

DR-HO'S Pain Therapy System Pro is a versatile device for pain relief. It uses TENS, EMS, and AMP to target and alleviate pain. Easy to use with customizable settings for...

Article on PSP awareness in Star Weekly Australia

Article on PSP awareness in Star Weekly Australia

Laura Louizos

Exciting News from the Coleen Cunningham Foundation!   We are thrilled to announce that a fantastic article on PSP awareness has been published in an Australian newspaper, organized by Peter...

1 comment

Article on PSP awareness in Star Weekly Australia

Laura Louizos

Exciting News from the Coleen Cunningham Foundation!   We are thrilled to announce that a fantastic article on PSP awareness has been published in an Australian newspaper, organized by Peter...

1 comment
Navigating Atypical Parkinsonism: Misdiagnosis Challenges and Family Frustrations

Navigating Atypical Parkinsonism: Misdiagnosis ...

Laura Louizos

Challenges in diagnosing atypical parkinsonism. Misdiagnosis issues and their impact on families. Common symptoms mistaken for other diseases. The importance of specialized medical expertise. How families can advocate for accurate...

Navigating Atypical Parkinsonism: Misdiagnosis ...

Laura Louizos

Challenges in diagnosing atypical parkinsonism. Misdiagnosis issues and their impact on families. Common symptoms mistaken for other diseases. The importance of specialized medical expertise. How families can advocate for accurate...

Understanding Progressive Supranuclear Palsy: Symptoms, Management Tips, and FAQs

Understanding Progressive Supranuclear Palsy: S...

Laura Louizos

- Progressive Supranuclear Palsy (PSP) is a rare neurological disorder affecting movement, balance, and eye movements. - Symptoms include stiffness, balance issues, difficulty moving eyes, speech and swallowing difficulties, and...

Understanding Progressive Supranuclear Palsy: S...

Laura Louizos

- Progressive Supranuclear Palsy (PSP) is a rare neurological disorder affecting movement, balance, and eye movements. - Symptoms include stiffness, balance issues, difficulty moving eyes, speech and swallowing difficulties, and...

Planning the Perfect Respite Vacation Program in Barbados for Individuals with Atypical Parkinsonism and Their Caregivers

Planning the Perfect Respite Vacation Program i...

Laura Louizos

As the founder of the Coleen Cunningham Foundation, I'm always seeking new ways to support families affected by Atypical Parkinsonism. One exciting initiative we’re planning is a respite vacation program...

Planning the Perfect Respite Vacation Program i...

Laura Louizos

As the founder of the Coleen Cunningham Foundation, I'm always seeking new ways to support families affected by Atypical Parkinsonism. One exciting initiative we’re planning is a respite vacation program...

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.