Père Rizk Foundation for PSP Awareness & Support

Père Rizk Foundation for PSP Awareness & Support Père Rizk Foundation started in January 2021 to help support & spread awareness about PSP in Lebanon. Who we are! We tracked symptoms as far back as 2009.

Our Dad (Père Rizk Rizk) was officially diagnosed in late 2013 with PSP after being misdiagnosed for a couple years. He rapidly progressed after official diagnosis and peacefully passed away in the evening of January 4, 2021. We struggled to find resources and supports for this rare neurological disorder. It was very frustrating and discouraging for all of us. We decided to make it our mission to

find and provide the best care and resources for our Dad. And hereby we are starting to raise awareness for this rare disease and are passing along our knowledge and experience in hopes it will help others! Our Goal is to reach and support all those suffering and in need of support with PSP: patients, their families and caregivers. What is PSP? Progressive Supranuclear Palsy (PSP) is an uncommon brain disorder that affects movement, control of walking (gait) and balance, speech, swallowing, vision, mood and behavior, and thinking. The disorder’s long name indicates that the disease worsens (progressive) and causes weakness (palsy) by damaging certain parts of the brain above nerve cell clusters called nuclei (supranuclear).

Raising awareness 🩵
11/01/2026

Raising awareness 🩵

👁️ Visual Signs & Symptoms of Progressive Supranuclear Palsy (PSP) 👁️

Progressive Supranuclear Palsy (PSP) is a rare, degenerative brain disorder and the second most common condition associated with parkinsonism, affecting movement, balance, and vision.

While PSP can be difficult to diagnose, visual signs and symptoms often help distinguish it from related disorders such as Parkinson’s disease, multiple system atrophy, dementia with Lewy bodies, and corticobasal degeneration.

Common visual signs of PSP may include:
🔹 Difficulty moving the eyes up and down (vertical supranuclear gaze palsy)
🔹 Trouble maintaining steady eye fixation
🔹 Wide-eyed or staring appearance due to eyelid retraction
🔹 Involuntary eyelid spasms (blepharospasm)
🔹 Difficulty opening or closing the eyes on command (apraxia of eyelid movement)

These visual challenges can significantly affect daily life, balance, and safety—often contributing to falls, especially backward falls.

👓 Early recognition matters. Eye-care professionals play an important role in identifying these visual symptoms and working alongside patients and caregivers to support visual health and quality of life.

💙 Raising awareness helps improve understanding, diagnosis, and care for those living with PSP.

04/01/2026
It’s very encouraging to hear about the important work at   on PSP research. This effort will surely help to better unde...
04/01/2026

It’s very encouraging to hear about the important work at on PSP research. This effort will surely help to better understand this disease and hopefully help families in the future!

Please check the flyer below and share it with your connections🙏

Would you know any patients or families open to connect with AUB research lab and get involved?

Thank you

Never forgotten🙏 Celebrating your birthday in Heaven🌹❤️
02/04/2025

Never forgotten🙏 Celebrating your birthday in Heaven🌹❤️

20/06/2023

Progressive Supranuclear Palsy (PSP) is a complex neurological disorder that affects each individual uniquely. While the journey may differ from person to person, medical professionals often categorize the progression of PSP into four broad stages. In this blog post, we will explore these stages to provide a comprehensive understanding of the disease’s trajectory.

Stage 1: Early PSP

In the early stages of PSP, the symptoms might be quite subtle and easily mistaken for normal aging or other neurodegenerative disorders. Some early signs may include:

-Frequent unexplained falls, typically backwards
-Difficulty with balance and mobility
-Changes in personality, such as increased apathy or mood swings
-Mild issues with eye movement, specifically in controlling upward and downward gaze

During this stage, it's common for individuals to be misdiagnosed with conditions such as Parkinson's disease or even simple aging-related issues. The accurate diagnosis of PSP at this stage can be challenging due to the overlap of symptoms with other conditions.

Stage 2: Mid PSP

As the disease progresses to the mid-stage, the symptoms become more pronounced and start to interfere with daily life. These may include:

-Increased difficulty with eye movements, often leading to blurred or double vision
-Noticeable changes in gait and balance, with frequent falls becoming a major concern
-Difficulty with speech and swallowing, leading to slurred speech and potential choking hazards
-Increased apathy and emotional changes

During this stage, the typical symptoms of PSP become more evident, often leading to a more accurate diagnosis if one hasn't been made already.

Stage 3: Advanced PSP

In the advanced stages of PSP, the symptoms can become severe and significantly affect an individual's quality of life. They may include:

-Severe difficulties with eye movements, sometimes leading to a complete inability to control eye gaze
-Increased difficulty with balance and mobility, often requiring assistive devices for movement
-Severe speech and swallowing issues, often necessitating a modified diet or feeding assistance
-Cognitive issues, such as slowed thought processes and mild memory problems

At this stage, comprehensive care and assistance become crucial for maintaining the individual's comfort and dignity.

Stage 4: Late PSP

The late stage of PSP is the most severe. Individuals at this stage may be largely immobile and require full-time assistance. The symptoms can include:

-Complete loss of eye movement
-Inability to walk or stand, requiring a wheelchair for mobility
-Severe speech and swallowing issues, potentially requiring tube feeding if chosen (always consult with healthcare professionals)
-Significant cognitive impairment

In this final stage, palliative care strategies are employed to ensure the individual's comfort. The focus shifts from treating symptoms to improving the quality of life and providing support to both the individual and their loved ones.

While PSP is a challenging journey, understanding these stages can help patients and their families prepare for the road ahead. A comprehensive, stage-based approach can aid in implementing timely and appropriate care strategies, enhancing quality of life, and fostering hope and resilience along the way.

Although PSP currently has no cure, the value of education, research, community support, and comprehensive care cannot be overstated. Through advancements in medical science and a deeper understanding of PSP, we hope for a future where this condition can be effectively managed, or even cured.

No One Walks Alone!

Head over to our blog for more, www.pspawareness.com/blogs/psp-q-a

31/05/2023

Cherishing Each Day: Embracing Life with a PSP Diagnosis

Life is an extraordinary gift, and it is often during our most challenging moments that we come to truly appreciate its value. When faced with a Progressive Supranuclear Palsy (PSP) diagnosis, the importance of cherishing every day becomes even more profound. It's a reminder that time is a precious and fleeting commodity, and each moment holds immeasurable worth.

PSP, a rare neurodegenerative disease, brings with it uncertainty and a range of physical and cognitive challenges. The prognosis varies from person to person, and it is impossible to predict how long one may live with the condition. My mom was told she had 2-6 years at diagnosis but unfortunately she passed away 6 months later. As my experience with my mom exemplifies, the timeline can be unpredictable, defying medical expectations.

Knowing this, it becomes essential to embrace the present, to live fully in the here and now. It means savoring the simple joys, finding gratitude in the smallest of moments, and treasuring the connections we have with our loved ones. It means recognizing that every day is a precious opportunity to create memories, share laughter, and show love.

In the face of adversity, we discover the resilience and strength within us. It is in these moments that we find the courage to make the most of the time we have, even when faced with the challenges that PSP brings. Embracing each day is about finding meaning and purpose, whether it's through pursuing passions, spending quality time with family and friends, or engaging in activities that bring us joy.

My mom's journey taught us that life is not measured solely by the number of years lived, but by the depth of experiences and the impact we make on others. She reminded us that every day is a chance to leave a lasting legacy, to touch lives with love and compassion. Though her time was cut short, the imprint she left on our heart and the memories we shared will endure forever.

Let us be reminded by my mom's story and honor her spirit by cherishing each day, not just for ourselves but also for those who have been affected by PSP. Let us advocate for greater awareness and support, so that others may receive the care and resources they need on their own journeys.

Remember, even in the face of uncertainty, we have the power to choose how we embrace each day. Let us live with gratitude, love, and the determination to make every moment count. Together, we can make a difference, raising awareness, supporting research, and cherishing each day as the precious gift it truly is.

Laura Louizos


Hopefully we will have soon more research on PSP…
24/01/2023

Hopefully we will have soon more research on PSP…

It has been said there are four stages, but because there is so little research they are a guideline only. Many people experience some stage four symptoms at stage one or overlap stages. Some never experience certain symptoms and then others can experience ones not listed. The impact it has on each....

Two years already… like it was yesterday 😢دايم دايم بالقلب 💙💙
05/01/2023

Two years already… like it was yesterday 😢

دايم دايم بالقلب 💙💙

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