Isn’t Parkinson’s Degenerative? How Can Michael J. Fox Be Better?

Actor Michael J. Fox in a 1988 photo (Wikimedia Commons)

“Great news,” I thought when I read that Michael J. Fox was returning to a comic television role, 12 years after he left to focus on treating his own Parkinson’s disease and funding research to help all patients.

“But how can this be? If there’s a big breakthrough in Parkinson’s disease treatment, wouldn’t we have heard about it? And if there isn’t one, isn’t the definition of a degenerative disease that it goes downhill? How can he have climbed back up again?”

Dr. Michael Schwarzschild, a Parkinson’s expert and director of the Molecular Neurobiology Laboratory at the MassGeneral Institute for Neurodegenerative Disease, kindly fielded my questions. First the disclaimers: He is not involved in Fox’s treatment, and has received grant support from the Michael J. Fox Foundation for Parkinson’s Research. Now the answer to my first query: What could it mean that Fox told ABC he “kind of stumbled onto a new cocktail of meds” that made him better enough to work again? Dr. Schwarzschild:

I heard his quote, too, and of course it’s wonderful that he’s making a comeback. In terms of what to make of this somewhat cryptic comment, I don’t think it relates to some new treatment that others don’t know about, or something newly approved and dramatic, because there isn’t anything like that.

‘Someone can improve without breaking the laws of physics about Parkinson’s disease being an inexorably progressive disorder.’

As a clinician who treats patients with Parkinson’s, your impression is right: It’s a progressive neurodegenerative disease. On average, in typical or even not-typical Parkinson’s disease, it’s inexorable.

That being said, it’s not a constant decline even though it goes in that direction, and medication can have a huge effect. Levodopa, when it came around in the sixties and seventies, took people out of nursing homes. Usually, with someone who’s getting reasonable care, you don’t expect, late in the disease, to discover some combination of currently available medications that make a huge difference. But sometimes you do.

I’ll give you a couple of examples even with approved medications in the United States. People will often get a good response to the standard medication and as the disease progresses they’re still getting a good response but having more and more symptoms. A substantial number of people develop a complication of medications called dyskinesias – abnormal involuntary twisting or flitting movements, which were on full display in some prior public appearances of Michael J. Fox.

For people who have that sort of problem, there are some medication approaches that can bring a dramatic benefit. There’s a medication called amantadine which is probably the only standard anti-Parkinson’s medication that can improve dyskinesias rather than make them worse. For most people with Parkinson’s, amantadine is not a first-line therapy because they don’t tolerate it that well or only in low doses, but for some it’s just the right combination where they tolerate it very well and it has a good effect on both their dyskinesias and their typical symptoms of Parkinson’s disease.

Surgery for deep brain stimulation is another example, where someone may be doing very poorly and for a subset of patients, the response is very good. Someone can improve without breaking the laws of physics about Parkinson’s disease being an inexorably progressive disorder.

Another example: Sometimes someone is on a standard drug regimen, and there’s a whole assortment of adjustments to that standard regimen: they can take a medication every few hours to smooth out their responses, or they can take a medication that will make the standard medication last longer. There are currently something like 12 medications that are approved for just the motor symptoms of Parkinson’s disease, and sometimes there’s a combination that will be very helpful.

So again, being completely naive to what the basis is for his improvement, it’s not crazy given the fact that our symptomatic medications, while only partially helpful, can be helpful and sometimes dramatically so, either alone or in combination.

It can be worth it to pursue trial and error — carefully.

It’s also probably a good example that when things get complicated and advanced, it’s good to work with a clinician who has some experience with that arsenal. It can be worth it to pursue trial and error — carefully.

So is that potentially the broader lesson, I asked, to to keep trying?

It could be that this reinforces the idea that you shouldn’t give up. Even the medications we do have — although they’re not good enough and we need to strive to improve them — we still have the benefit in Parkinson’s disease of some very effective medications. And for the right people in the right combination, it really can make a difference, to work with your physician to find that right mix and balance.

And the pipeline for possible new medications?

There’s a tremendous amount of hope, and the pipeline is not bad. But there’s nothing on the verge of FDA approval despite exciting earlier stage prospects. There’s a range of novel candidate therapies under investigation, from gene therapy to antioxidants to modifications of old things in new forms that can impact the dopamine system, like caffeine.

One thing I’ll mention: An example of something that is close and a surprisingly good example of using what we have available more effectively to make a big difference: There’s a new formulation for levodopa given continuously by pump. It’s on the market in Europe and undergoing FDA review here. The preliminary reports from higher-level clinical trials look quite remarkable. These are the kinds of things that, even later in the disease, for patients who have fluctuations, can make a big difference.

  • http://twitter.com/lost2shadow Lost 2 Shadow

    Are physicians aware that parkinson’s and the medications being provided are also being blamed for a child being molested in Michigan???? I just wonder if any one cares about that.

  • Tina

    i am 43 with pd, was diag 3 yrs ago and progressing fast. wihtin that short amt of time i became disabled and am up to taking my meds every 2 hrs…sinemet and mirapax and i still have alot of down time where i can’t do anything….move, walk, etc. need assistance from hubby for normal daily routines we all take for granted.. and the side effects from taking meds are miserable. i walk w/cane or walker and have scooter. i have alot of the bad symptoms,stiffness, slowness of movement, very poor balance & coordination., but no tremors… I fall all the time…have alot of bumps and bruises…..only a matter of time before i really hurt myself. why is it a secret about michael’s new drug regimen and/or treatment. why is he not disclosing this info.? His old drug regimen was disclosed, which one was sinemet. Maybe all or some of us can try and beneft from it. Is this some kind of new treatment in clinical trials not yet approved by the FDA? I have been reading up on gene therapy and sounds very promising, I’m going to talk with my new doc. at my next appt and see if i can get into a clinical trial for gene therapy. Please help us Michael ! You look great and also look like you you feel great! I don’t want to have to be put into nursing home at 50 just bec. that is one neurologist (movement disorder specialist) told me. I have a life to live. I just want a bettert quality of life, as we all do in the PD comunity. He was concerned at the rate i was progressing and how disabling my symptoms had become.

  • http://www.facebook.com/people/Imani-Burrell/100002259534084 Imani Burrell

    …or, he’s finally learned that parasites might very well be what was causing his symptoms…
    http://www.rightdiagnosis.com/n/neurocysticercosis/intro.htm

  • mikeklem

    Is caffine good or bad to have when taking levodopa ? — I’ve been diagnosed with PD since February — I’m 69 year old — Have temors only in my left hand (at times) —

    • http://www.facebook.com/MargaritaFriedman Margarita Friedman

      Mike, Try this. It works. When the tremor starts, immediately command you arm (or leg) to STOP while you watch each muscle tighten. Stretch you arm as far as you can, bend your hand backwards and open your fingers, rotate your hand to the right and left as if waxing a car. Look at your muscles while you say aloud ARM STOP, DO NOT SHAKE” Hold as much as you can and let go, if it is still shaking, repeat. What you are doing is creating new healthy synapsis through bundles of muscle cells that have not yet been damaged. By tightening, you are making those bundles stronger and will be able to subdue the “rioters”. You are consciously using your brain to command, with the help of your sight and hearing.

  • PD patient

    Many of us with Parkinson’s have been curious to know what MJF stumbled upon. The scenario Dr. Michael Schwarzschild lays out sounds very plausible.

    In my 14+ years since diagnosis, I don’t know that I have ever seen the reality of the disease so well described. This succinct overview of the course of PD and the array of treatments is one of the best pieces I have read.

    To feel one’s condition is understood is therapeutic in itself. Thank you, Carey Goldberg and Dr. Schwarzschild!

  • Optimist

    Please, Michael, tell us what it is so that we can try it, too! You are the most trusted person in the Parkinson’t community. We count on you!!

  • Sue K

    Carey, Thanks for asking this question. I was wondering the same thing. The answers you found show the complexity of these neurological diseases but also show that there’s reason for hope. The road to true disease modification is slower than we’d all like but it pays to stay with it. Look at Tay-Sachs where the defective gene was discovered many years ago. Finally we’re on the verge of starting gene therapy human clinical trials!