Dem Congresswoman Says She Has ‘Parkinson’s on Steroids,’ Will Finish Her Term
A Democratic Congresswoman Battles “Parkinson’s on Steroids” and Vows to Finish Her Term
Virginia Representative Jennifer Wexton is facing a formidable opponent: progressive supranuclear palsy (PSP), a rare neurological disorder with no cure. Despite her diagnosis, Wexton is determined to serve out her current term, which concludes in January 2025, according to CBS News.
At 55 years old, Wexton has experienced a decline in her condition since September, leaving her exhausted and frustrated. In a recent tweet, she expressed her frustration with the disease and her determination to continue serving her constituents in Virginia’s 10th district.
Like I said when I announced my PSP diagnosis, this disease sucks.
It’s been a difficult journey but I’m working as hard as ever to serve #VA10.
I’m sharing my experience to raise awareness of what PSP is and why it’s so important to find a cure. https://t.co/xqx8Iog4or
— Rep. Jennifer Wexton (@RepWexton) November 18, 2023
The recent tumultuous 10-week session in the House, which included the threat of a federal shutdown and the election of a new speaker, took a toll on Wexton. The constant tension and demanding floor votes weakened her, leading to a fall that injured her neck.
Due to her condition, Wexton now struggles to speak clearly, making it difficult for her colleagues to understand her. Despite this setback, she remains cognitively sharp and eager to participate in conversations.
Recognizing the challenges Wexton faces, her chief of staff, Abby Carter, sent a letter to fellow lawmakers advising them to ask Wexton to repeat herself or provide written communication if necessary.
In an interview with The Washington Post, Wexton expressed her frustration and the unfairness of her situation. She even asked her doctor if she could still run for re-election after her diagnosis, to which he questioned why she would want to.
According to the National Institutes of Health, PSP affects body movements, walking, balance, and eye movements. The disease typically progresses rapidly, leading to severe disability within three to five years of symptom onset. Complications such as pneumonia, choking, and falls resulting in head injuries are common.
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Despite the challenges Wexton faces, she remains determined to make a difference while she is still able. She has been an advocate for gun control and healthcare reform, and has worked tirelessly to improve the lives of her constituents. Wexton’s dedication to her work has not wavered, even in the face of a debilitating illness.
While there is currently no cure for PSP, Wexton is using her platform to raise awareness about the disease and the need for research funding. She hopes that by sharing her experience, she can help others understand the impact of rare neurological disorders and the importance of finding a cure.
Wexton’s decision to continue serving her term despite her diagnosis is a testament to her strength and commitment to public service. Despite the physical and emotional toll of her illness, she refuses to let it define her or prevent her from fighting for what she believes in.
As Wexton battles “Parkinson’s on steroids,” she serves as an inspiration to others facing their own health challenges. Her determination to keep going and make a difference is a reminder that even in the face of adversity, we can still find the strength to persevere.
Jennifer Wexton’s story serves as a powerful reminder of the resilience and determination of individuals facing debilitating illnesses. Her commitment to public service and her refusal to let her diagnosis define her is an inspiration to us all. We wish her strength and continued success as she fights for her constituents and raises awareness about progressive supranuclear palsy.
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