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An Interview with Lonnie Ali

LA:  Support groups can be extremely important, not only for connecting on a social level, but also for supporting the whole caregiver process, and the notion of taking care of that patient.  If someone has already been through an experience, they can connect with other caregivers, telling them what they can do to meet those challenges so that they are able to manage better.  I would never diminish the importance of a caregiver support group in the community because it’s an essential component of caregiving.  Not every community has a Parkinson’s caregiver support group, but where they exist, they are valuable and it’s a meaningful resource that people should take advantage of.

GB:  Why do you think family involvement is so very important in the well-being of someone living with Parkinson’s disease?

LA:  It’s important for the family to be educated with regards to Parkinson’s disease because they need to understand what that patient is going through and what the caregiver is going through. It’s important to involve family members and also to realize that the caregiver is going to need relief as well. They need people to come in and give them time so that they can be away, so that they can do things that they want to do.  It’s great when you have family that is nearby who can offer that kind of assistance and support to you.

GB:  What role do you see spirituality playing in being a caregiver for your loved one?

LA:  You never know why you are given a certain cross to bear. Sometimes you feel like you’re in this fight alone, but I think that if you have a strong spiritual base, that there’s always going to be a higher being there to support you and that you can always turn to. It’s been a very important thing in my life, and in my husband’s life, and I don’t want to be preachy, but it is just a part of our life; and I think that it is almost a foundation in the lives of many caregivers. You have to realize that we’re all here for a reason, even in your role as a caregiver.  It’s keeping that positive attitude and not letting it get you down, because you never know, you may be the example for someone else; and what you’re doing may not just help yourself, but thousands of others. My husband felt that way, and I’m sure Michael J. Fox felt that way in his fight for Parkinson’s research; and because of their celebrity, they’ve been able to garner a lot of money for research, not only from Congress, but from private, individual, philanthropic donations. So, you never know why you have something, and my husband’s attitude has been, “I work with the cards dealt me, but I don’t let it define who I am, and I don’t let it stop me from doing what I want to do and what I need to do.”

GB:  The work that you, your husband and your family as well as Michael J. Fox and his family are doing has helped to make the discussion so public. And as I talk to caregivers and people living with Parkinson’s disease, it all means so much to them.  I think it is extremely morale-boosting for caregivers.

LA:  Exactly, it is a morale booster, because I know that people look to Mohammed and I, and to Michael J. Fox to give them the right information and to give them the right resources.  It’s just a wonderful opportunity for me, as a caregiver, to share with others who are doing the same thing that I am doing.

GB:  If you were able to give just one piece of advice to family caregivers, what would that advice be?

LA:  Make sure you find the best Parkinson’s specialist that you can get for your Parkinson’s patient. Make sure you get the right pharmaceutical treatment as well. Make sure you’re aware of what’s out there and are able to utilize that information when you go in to see that Parkinson’s specialist.  Ask those kinds of questions about what’s new and what you can do to improve the quality of life for your loved one.