Parkinson’s Disease

Adam Jogee Excerpts

Monday 17th November 2025 Westminster Hall

[Adam Jogee (Newcastle-under-Lyme) (Lab)]

I congratulate my hon. Friend the Member for Colne Valley (Paul Davies) on his excellent opening speech. In June this year, my father-in-law, Adrian Lawther, died after living with Parkinson’s for more than a decade. Adrian was a smart, decent and unassuming man, and very much lived the lessons of “two eyes and one mouth”. He did not miss a trick and spied everything, but only ever spoke when he needed to—a lesson he never managed to teach me, but one that I suspect quite a few of us around here would benefit from. He had an interest in the world around him and the world far overseas, and was incredibly kind and welcoming to me—which is no guarantee when marrying someone’s daughter. But for all the memories, the love, the grief and the sadness, we also saw up close the cruel impact of Parkinson’s on a person’s dignity and their quality of life, and on those around them.

[Graeme Downie]

I thank my hon. Friend for the moving way he has talked about his father-in-law. Does he agree that what he has said emphasises the need to make sure that families are also supported during Parkinson’s care?

[Adam Jogee]

I could not have put that better myself.

In Newcastle-under-Lyme, hundreds of local people live with Parkinson’s, and that number is rising. It is a life-altering disease that destroys personal autonomy; it affects someone’s ability to talk, swallow, move and write. Cruel is not the word. For those who are suffering and need treatment now, the lack of care provision and the inaccessible treatment is simply unacceptable.

I think of my friend Alderman Lizzie Shenton, a former leader of Newcastle-under-Lyme district borough council, who I saw just last week. She has been diagnosed with the early onset of Parkinson’s in her 50s. She is very healthy and still has much do to. Lizzie had to wait 10 months for a consultant appointment to make a formal diagnosis, and she has been waiting for her DaT scan for five months, without which no medication or treatment can be prescribed.

I pay tribute to the fantastic work being done by the North Staffs Parkinson’s UK branch—the chair, Lorraine, the treasurer, Councillor David Grocott and the whole committee who do wonderful things week in and week out. I thank the Dubb family from the Westlands in Newcastle-under-Lyme for their annual fundraising 5k run and a massive cookout at their home—which smelled very good—all raising money for Parkinson’s UK. My constituent Julie Hibbs has long campaigned to add Parkinson’s to the medical exemption list. The Minister knows that I support those calls—I have raised them with her and others, and I will continue to do so.

The funding and availability of care for Parkinson’s patients do not match the severity of this disease and the desperate need for proper treatment. Getting those suffering from Parkinson’s the right care at the right time is critical to ensuring that their quality of life is as high as it can be, and that the cost of providing that is used as efficiently as possible. As more and more of us get Parkinson’s, those who will suffer from it and their loved ones deserve to know that the question of getting the right treatment is not one they will ever have to worry about.

[Emma Lewell (in the Chair)]

I am terribly sorry; we are not able to take any more Back-Bench speeches. I call the Liberal Democrat spokesperson.