Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
A Heartfelt Thank You to Our Support Group Members
As we close the curtains on this year, I want to extend a massive thank you to each and every one of you who have been a part of our...
A Heartfelt Thank You to Our Support Group Members
As we close the curtains on this year, I want to extend a massive thank you to each and every one of you who have been a part of our...
Caregiver's Corner: Supporting Loved Ones with ...
Atypical Parkinsonism encompasses a group of neurodegenerative disorders that share some symptoms with Parkinson's disease but have distinct characteristics and challenges. These conditions, including Multiple System Atrophy (MSA), Progressive Supranuclear...
Caregiver's Corner: Supporting Loved Ones with ...
Atypical Parkinsonism encompasses a group of neurodegenerative disorders that share some symptoms with Parkinson's disease but have distinct characteristics and challenges. These conditions, including Multiple System Atrophy (MSA), Progressive Supranuclear...
Therapies and Treatments: Atypical Parkinsonism
Atypical Parkinsonism refers to a group of neurological disorders that share some similarities with Parkinson's disease but have distinct features and progress differently. Managing the symptoms of atypical Parkinsonism can...
Therapies and Treatments: Atypical Parkinsonism
Atypical Parkinsonism refers to a group of neurological disorders that share some similarities with Parkinson's disease but have distinct features and progress differently. Managing the symptoms of atypical Parkinsonism can...
Heartfelt Thanks to Our Amazing Volunteers!
🙏 As we express our deepest gratitude, we want to shine a spotlight on two extraordinary individuals who are the heart and soul of our community - Kate Borgert and...
Heartfelt Thanks to Our Amazing Volunteers!
🙏 As we express our deepest gratitude, we want to shine a spotlight on two extraordinary individuals who are the heart and soul of our community - Kate Borgert and...
AlphaLift Mobility Lifter: A Game-Changer for P...
Living with Progressive Supranuclear Palsy (PSP) presents numerous challenges, affecting one's mobility and independence. Among the many difficulties PSP patients face, transportation can be particularly daunting. Traditional mobility solutions like...
AlphaLift Mobility Lifter: A Game-Changer for P...
Living with Progressive Supranuclear Palsy (PSP) presents numerous challenges, affecting one's mobility and independence. Among the many difficulties PSP patients face, transportation can be particularly daunting. Traditional mobility solutions like...
End of Year Meeting with Cookie Exchange!
Dear Members, As the year draws to a close, we’re excited to invite you to our last in person support group meeting of 2023, scheduled for November 27th at Port...
End of Year Meeting with Cookie Exchange!
Dear Members, As the year draws to a close, we’re excited to invite you to our last in person support group meeting of 2023, scheduled for November 27th at Port...
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.