Atypical Parkinsonism Blog
Many New Blog Posts Each Week
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Atypical Parkinsonism Blog by: Laura Louizos
Sleep disorders with PSP
These sleep disorders can be caused by the underlying neurodegenerative process of PSP, as well as by medications used to manage PSP symptoms.
Sleep disorders with PSP
These sleep disorders can be caused by the underlying neurodegenerative process of PSP, as well as by medications used to manage PSP symptoms.
Urinary incontinence with PSP
Urinary incontinence is the involuntary loss of urine, which can range from occasional leaking to a complete loss of bladder control.
Urinary incontinence with PSP
Urinary incontinence is the involuntary loss of urine, which can range from occasional leaking to a complete loss of bladder control.
Caregiving and PSP
It's important for caregivers to recognize that caring for someone with PSP can be a long-term and challenging journey.
Caregiving and PSP
It's important for caregivers to recognize that caring for someone with PSP can be a long-term and challenging journey.
Advanced Planning with PSP
Here are some advanced planning considerations for individuals with PSP and their families.
Advanced Planning with PSP
Here are some advanced planning considerations for individuals with PSP and their families.
PSP Trials
Clinical trials are an important way to advance our understanding of the disease and develop new treatments.
PSP Trials
Clinical trials are an important way to advance our understanding of the disease and develop new treatments.
Medications for PSP Symptoms
The medications used for PSP typically target the specific symptoms of the disease.
Medications for PSP Symptoms
The medications used for PSP typically target the specific symptoms of the disease.
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.