Ogemaw Parkinson's Support Group

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Ogemaw Parkinson's Support Group This page will provide information about the meetings, events, and speakers for the Ogemaw Parkinson's Support Group. It will be a forum for PD.

We are a group that provides support and information for parkinson's patients, caregivers, or for anyone wanting more information about parkinson's. We gather every second Tuesday of the month at 2:00-3:30 pm in the Executive Dining Room of the West Branch Hospital. It is immediately to the right as one goes into the Main Entrance.

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10/08/2026

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When Michael J. Fox took the stage at the 2026 Emmys to accept the Bob Hope Humanitarian Award, he glanced out into the audience and locked eyes with Tracy Pollan, his wife of 38 years. All four of their children sat right beside her. It was a quiet, triumphant moment 35 years in the making — one that traced all the way back to a 1991 doctor’s visit that rewrote their entire lives.

The pair married in 1988, welcomed their first son Sam a year later, and built the kind of sunny Hollywood life that looked unbreakable from the outside. Then in 1991, at just 29 years old, Michael went to a neurologist for a persistent twitching finger and an aching shoulder. He left with a Parkinson’s diagnosis.

He came home devastated and told Tracy the news. She didn’t offer hollow promises that everything would work out. She didn’t downplay the hard years ahead. She just spoke four soft, unshakable words: “In sickness and in health.” The same vow they’d said at their wedding, now suddenly weighted with a future neither had planned for.

For seven years, he kept the diagnosis hidden from the world, continuing to work in film and television while privately spiraling into alcohol to cope. He got sober in 1992, and began to face his reality head-on. Their family kept growing: twin daughters arrived in 1995, followed by a third daughter in 2001. When he finally went public in 1998, he turned his personal struggle into a global movement. The Michael J. Fox Foundation is now the world’s largest nonprofit funder of Parkinson’s research, having poured more than $3 billion into better treatments and a cure.

Thirty-five years later, he’s still leading that fight, and she’s still standing right beside him. Wedding vows are easy to say when the future looks bright. They only become real when life breaks open — and someone chooses to stay, every single day.

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10/08/2026

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Canada just gave Michael J. Fox its highest civilian honor for nearly three decades of fighting Parkinson's. Back in the U.S., where he built that fight, Washington spent most of last year with the Pentagon's Parkinson's research program at zero, and the White House now wants $5 billion cut from the National Institutes of Health.

Fox is 65 and rarely appears in public anymore. On Friday he made the trip to Rideau Hall in Ottawa, as reported by CBC and The Canadian Press, to be promoted to companion of the Order of Canada, a rank capped at 180 living people.

He's worn the white officer's pin for 16 years. Now he gets the red one.

When he was diagnosed, Fox was one of the biggest stars in Hollywood, and he hid it for years because he worried audiences would laugh at a sick man. He went public in 1998 anyway. Two years later he started a foundation that has since put more than $3 billion into Parkinson's research, more than any other nonprofit on Earth.

He kept working through tremors and balance problems. He made "Still," the 2023 documentary about his life with the disease, and last month, as People reported, the Emmys handed him the Bob Hope Humanitarian Award to a double standing ovation.

At Friday's ceremony, Governor General Louise Arbour borrowed his most famous film to say that "back to the future has always been a much better idea than forward to the past."

The U.S. has been going the other direction.

More than 110,000 American veterans are living with Parkinson's, according to the Parkinson's Foundation. The Pentagon runs one of the only federal programs dedicated purely to the disease, studying why troops exposed to herbicides and other chemicals get sick, a link the VA already recognizes.

In March 2025 a stopgap spending bill cut military medical research by 57%, as Roll Call and Stars and Stripes reported. Parkinson's got nothing.

The program came back in February with $16 million. Its funding had already been flat for a decade, and House members wrote that it was getting four to six times more applications than it could pay for.

That's the small money. The big money is the NIH, the country's main engine of medical research.

The White House's 2027 budget asks Congress to cut it by $5 billion. Fox's foundation and two other Parkinson's groups warned that would slow breakthroughs for the 1.2 million Americans living with the disease.

Last year the White House asked for a 40% NIH cut and Congress refused, so they're trying again.

Congress has pushed the decision past the midterms, and the stopgap money runs out December 11.

Fox isn't waiting on them. His foundation keeps funding the science Washington keeps shortchanging, and at 65, with the disease getting harder every year, he told People he feels privileged to spend his days "bringing everything I've got to help cure this disease."

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Address

Maysville, GA

Opening Hours

12:30pm - 2pm

Telephone

+19898362132

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