Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
Support Group Meeting - Burlington Ontario
This is a friendly reminder about our upcoming in person Atypical Parkinsonism Support Group Meeting. We value your experience and insights, and we look forward to your participation. Please find...
Support Group Meeting - Burlington Ontario
This is a friendly reminder about our upcoming in person Atypical Parkinsonism Support Group Meeting. We value your experience and insights, and we look forward to your participation. Please find...
Tim Talks on YouTube
Exciting news! The inaugural session of “Tim Talks” has just been released on YouTube. This isn’t just any session - it’s a deep dive into Tim’s personal journey with PSP...
Tim Talks on YouTube
Exciting news! The inaugural session of “Tim Talks” has just been released on YouTube. This isn’t just any session - it’s a deep dive into Tim’s personal journey with PSP...
Alleviating Symptoms: The Off-Label Use of Oral...
Using atropine drops orally to manage excessive secretions, including phlegm and saliva, is an off-label but often effective practice, especially in conditions like Progressive Supranuclear Palsy (PSP). PSP is a...
Alleviating Symptoms: The Off-Label Use of Oral...
Using atropine drops orally to manage excessive secretions, including phlegm and saliva, is an off-label but often effective practice, especially in conditions like Progressive Supranuclear Palsy (PSP). PSP is a...
Out of Office
Laura is currently out of the office and will return on October 23, 2023. Support group meetings WILL continue as scheduled!For immediate concerns please email info@coleencunninghamfoundation.com
Out of Office
Laura is currently out of the office and will return on October 23, 2023. Support group meetings WILL continue as scheduled!For immediate concerns please email info@coleencunninghamfoundation.com
Tim Talks
📣 Announcement 📣Join us for our inaugural "Tim Talk" on Thursday, October 26th 7-9pm Eastern Time. We are honored to present our distinguished guest speaker, a notable PSP warrior and leader....
Tim Talks
📣 Announcement 📣Join us for our inaugural "Tim Talk" on Thursday, October 26th 7-9pm Eastern Time. We are honored to present our distinguished guest speaker, a notable PSP warrior and leader....
Holidays and Progressive Supranuclear Palsy (PS...
Holidays are traditionally a time of joy, family gatherings, and celebrations. However, for families coping with a loved one diagnosed with Progressive Supranuclear Palsy (PSP), holidays can also bring a...
Holidays and Progressive Supranuclear Palsy (PS...
Holidays are traditionally a time of joy, family gatherings, and celebrations. However, for families coping with a loved one diagnosed with Progressive Supranuclear Palsy (PSP), holidays can also bring a...
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.