For better treatment and research for women with Parkinson's Disease

RAISING OUR VOICES

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There are more than 10 million people worldwide diagnosed with Parkinson's Disease. How many are women? What is the average age women are diagnosed? How do women react differently to medication than men? There are no clear answers. We need answers.

And so we started the Women's Parkinson's Project to raise our voices for better treatment and research for women with Parkinson’s disease.

The Women's Parkinson's Project

Women's Parkinsons' Project Women's Parkinsons' Project

Our First Webinar! 8th March 2022

We are excited to announce our first Webinar ever! Titled "Women with PD – Unmet Needs of Women Living with Parkinson’s Disease: The Gaps & Controversies" the Women’s Parkinson’s Project, will be presenting a robust discussion, sponsored by the World Parkinson Coalition!

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Sree Sripathy Sree Sripathy

From Four-Eyes to Eight

I've never been called four eyes. Maybe because I started wearing glasses only in high school. And even then, I barely wore them, constantly forgetting them, losing pair after pair in college. It would have been preparation for my current incarnation as an eight eyed being. Hindu goddesses are often depicted as having multiple arms and sometimes heads. I've always wanted to be a goddess. I may not have the multiple heads, but I do have the multiple eyes. Eight of them.

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Shanthipriya Siva Shanthipriya Siva

Depression and Balancing Life

A person might experience depression at any time during the journey with Parkinson's Disease, even before diagnosis. Depression in PD is due to chemical imbalances in the brain. I have had Young Onset Parkinson’s Disease since 2011. Maybe my symptoms of depression were not diagnosed earlier.

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Rebecca Miller Rebecca Miller

Three Days Before DBS

I like my brain. We’ve had a fairly good relationship over the years. It has generally served me well and has become more reliable with some teaching and training over the years. There are certain parts that are especially nice, the parts that put words together in interesting combinations, the parts that can convey feelings and images to others, the parts that entertain and find humor in many small and dark things, the parts that attempt to enter into someone else’s experience and project into another person’s world.

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Kat Hill Kat Hill

A Long Way to Go

I worked as a nurse, a nurse midwife-nurse practitioner and a clinical director in my first act. In that first act were the years that I had trained for and dreamed about serving women with reproductive health needs and helping to guide women through labor and delivery of their newborn babies and to help through many phases in their lives. Then I was diagnosed with Young Onset Parkinson’sDisease. I left my clinical work and now am an author, advocate and artist.

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Women's Parkinsons' Project Women's Parkinsons' Project

Building from Small Acorns

Women’s empowerment and women’s voices in healthcare have exploded on social media recently. When we started the Women’s Parkinson’s Project, we knew we wanted to address a need, a gap, we saw. That gap was a place to share the voices of women, through stories, about their day-to-day struggles and their journey with Parkinson’s Disease and other neurological conditions. We wanted to go slow. Give our project time to build up. We all had jobs, families, commitments, and of course our main partner to take care, the disease itself.

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Sree Sripathy Sree Sripathy

The Fastest Envelope Stuffer in the West

"Your disease is progressing," my doctor told me last June. I stared at her. I didn't understand. I was a slow progresser. Slow on the slow scale, the last snail in the race. I envisioned slow being where I was for the next twenty years. I knew that didn’t make sense. I knew I was partly in denial. But I held on to that belief. It got me through. I felt that I was given that magical fairy dust that would freeze the disease in time within my body.

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Richelle Flanagan Richelle Flanagan

A New Baby and a Diagnosis of Young Onset PD

So, there I was 3 months pregnant with a much wanted second child, having a hot chocolate on the side of a snowy mountain in the French Alps when my hand would not stop shaking. When my husband came off the slopes with my 10-year-old son, I remember saying to him ‘as long as it’s not Parkinson’s.’

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My Hands
Kat Hill Kat Hill

My Hands

We use our hands to function well in the world; to put on our clothes, to feed ourselves, to care for those we love. I have used my hands to help mamas bring their babes into this world. I was a honored to work as a midwife “catching” babies for over 15 years. A collection of old weathered hands hung on my office wall. Hands fascinate me; what stories might hands hold? What special touch were they a part of? Hands of the aged, what wisdom might they hold?

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Women's Parkinsons' Project Women's Parkinsons' Project

Birth of a Project

We do ourselves an injustice by just suffering through it. Life, that’s the it. Women, that’s the we. We are so busy juggling families, work, caring for elder parents and advocating for others that we forget to advocate for ourselves. And if we do not advocate for ourselves, who will?

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Our Team

  • Richelle Flanagan

    CO-FOUNDER

  • Kat Hill

    CO-FOUNDER

  • Sree Sripathy

    CO-FOUNDER