Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
Life Threatening Complications Associated with PSP
I’m truly sorry to hear that you’re seeking this information. It’s important to approach this topic with care and sensitivity but also honesty. Please reach out if you need support!...
Life Threatening Complications Associated with PSP
I’m truly sorry to hear that you’re seeking this information. It’s important to approach this topic with care and sensitivity but also honesty. Please reach out if you need support!...
PSP AWARENESS SHOP T-SHIRT GIVEAWAY!
🎉 PSP AWARENESS SHOP T-SHIRT GIVEAWAY! 🎉Attention all T-shirt lovers and advocates! We’ve got exciting news for you!👕 How to Enter:1. Like the Facebook post and photos. 2. Head to the...
PSP AWARENESS SHOP T-SHIRT GIVEAWAY!
🎉 PSP AWARENESS SHOP T-SHIRT GIVEAWAY! 🎉Attention all T-shirt lovers and advocates! We’ve got exciting news for you!👕 How to Enter:1. Like the Facebook post and photos. 2. Head to the...
Tough Conversations with a PSP Diagnosis
Progressive Supranuclear Palsy (PSP) is a rare and progressive brain disorder, often characterized by difficulty in walking, balance problems, and an inability to control eye movements. As with any progressive...
Tough Conversations with a PSP Diagnosis
Progressive Supranuclear Palsy (PSP) is a rare and progressive brain disorder, often characterized by difficulty in walking, balance problems, and an inability to control eye movements. As with any progressive...
The Power of Support Groups for Caregivers of P...
Progressive supranuclear palsy (PSP) is a rare neurological disorder that remains, unfortunately, lesser known in the medical community. While professionals continue to unravel its intricacies, caregivers are often left to...
The Power of Support Groups for Caregivers of P...
Progressive supranuclear palsy (PSP) is a rare neurological disorder that remains, unfortunately, lesser known in the medical community. While professionals continue to unravel its intricacies, caregivers are often left to...
🌟 Reminder: Support Group Meeting Tonight! 🌟
Hey everyone,Don't forget about our Zoom Support Group meeting from 7-9pm ET this evening! Just a click away, you can join us right from the comfort of your home.🔗 Message...
🌟 Reminder: Support Group Meeting Tonight! 🌟
Hey everyone,Don't forget about our Zoom Support Group meeting from 7-9pm ET this evening! Just a click away, you can join us right from the comfort of your home.🔗 Message...
Patience and Empathy: Understanding PSP and Its...
Living with or caring for someone with Progressive Supranuclear Palsy (PSP) is a journey that can be both emotionally and physically demanding. PSP, a neurodegenerative disease, not only affects movement...
Patience and Empathy: Understanding PSP and Its...
Living with or caring for someone with Progressive Supranuclear Palsy (PSP) is a journey that can be both emotionally and physically demanding. PSP, a neurodegenerative disease, not only affects movement...
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.