Atypical Parkinsonism Blog

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Atypical Parkinsonism Blog by: Laura Louizos

Dr. Gabor Kovacs of UHN’s Krembil Research PSP

Tracing the paths to disease (PSP)

Laura Louizos

The study, led by Dr. Gabor Kovacs of UHN’s Krembil Research Institute, maps the regions of the brain where pathological tau proteins arise in individuals with various sub-types of progressive supranuclear...

2 comments

Tracing the paths to disease (PSP)

Laura Louizos

The study, led by Dr. Gabor Kovacs of UHN’s Krembil Research Institute, maps the regions of the brain where pathological tau proteins arise in individuals with various sub-types of progressive supranuclear...

2 comments
Canadian Tax Help for Disabled Individuals

Canadian Tax Help for Disabled Individuals

Laura Louizos

Canadian disability tax credit! Have you applied? It can help with those extra medical expenses.Once you apply and are approved you are able to claim it each year and do...

Canadian Tax Help for Disabled Individuals

Laura Louizos

Canadian disability tax credit! Have you applied? It can help with those extra medical expenses.Once you apply and are approved you are able to claim it each year and do...

CORD presents Rare Disease Drug Strategy Webinars

CORD presents Rare Disease Drug Strategy Webinars

Laura Louizos

PMPRB: Friend or Foe of Rare Disease Drug Strategy In February 2019 the federal government committed $1billion over two years starting in 2022 to set up a Canadian Rare Disease...

CORD presents Rare Disease Drug Strategy Webinars

Laura Louizos

PMPRB: Friend or Foe of Rare Disease Drug Strategy In February 2019 the federal government committed $1billion over two years starting in 2022 to set up a Canadian Rare Disease...

RETROTOPE UPDATE RT001 Drug Trial

RETROTOPE UPDATE RT001 Drug Trial

Laura Louizos

US FDA Allows Trial to Proceed for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP).LOS ALTOS, CALIF, April 25, 2020– Retrotope announced today that it received a “Study...

RETROTOPE UPDATE RT001 Drug Trial

Laura Louizos

US FDA Allows Trial to Proceed for Retrotope’s RT001 in the Treatment of Progressive SupraNuclear Palsy (PSP).LOS ALTOS, CALIF, April 25, 2020– Retrotope announced today that it received a “Study...

Association of Stress-Related Disorders

Association of Stress-Related Disorders

Laura Louizos

Association of Stress-Related Disorders With Subsequent Neurodegenerative Diseases By: Huan Song, MD, PhD; Johanna Sieurin, MSc; Karin Wirdefeldt, MD, PhD Original Investigation | March 9, 2020 Key Points Question  Do...

Association of Stress-Related Disorders

Laura Louizos

Association of Stress-Related Disorders With Subsequent Neurodegenerative Diseases By: Huan Song, MD, PhD; Johanna Sieurin, MSc; Karin Wirdefeldt, MD, PhD Original Investigation | March 9, 2020 Key Points Question  Do...

Clinical trials RT001 for PSP-UPDATE

Clinical trials RT001 for PSP-UPDATE

Laura Louizos

RETROTOPE UPDATE! I will be meeting with the RETROTOPE team tomorrow March 5th in California and will provide an update shortly after. In the interim here is an update from Sarah...

Clinical trials RT001 for PSP-UPDATE

Laura Louizos

RETROTOPE UPDATE! I will be meeting with the RETROTOPE team tomorrow March 5th in California and will provide an update shortly after. In the interim here is an update from Sarah...

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.