A web-blog (formerly known as Stu's Views and MS News), now published by MS Views and News, a patient advocacy organization. The information on this blog helps to Empower those affected by Multiple Sclerosis globally, with education, information, news and community resources.
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Saturday, August 5, 2017
The Importance of Patients Having a Voice in MS Research
I recently spent time at the annual meeting of the Drug Information Association (DIA), listening to presentations and talking with industry representatives about the multiple sclerosis community’s needs.
DIA is a nonprofit association that has been around more than 50 years. Their primary interest is the development of healthcare products — drugs and devices — and supporting innovation in these areas. It has only been in the past decade that patient advocates have been included in the DIA’s annual meeting, and last year I attended as a DIA Patient Fellow.
The theme for DIA 2017 was “Driving Insights to Action.” And as its website noted, DIA “is the only global organization dedicated to bringing health care product development professionals together in a trusted, global, neutral environment to share insights and drive action in health care product development and life cycle management.”
Although DIA has made a commitment to including a patient advocate’s voice in their meetings and work, I would be less than honest if I didn’t say at times it feels like an uphill climb. Even their statement about DIA 2017 “Driving Insights to Action” includes only professionals in healthcare product development, and no mention of the people they are meant to serve.
Another example is that a unique Patient Engagement track of courses offered this year won’t be offered at DIA 2018. I’m told that instead, they will push hard to have patients’ voices infused into more of the other sessions. While I continue to be skeptical, I will give them the benefit of the doubt because I really want this new collaboration to grow and improve. We need the drug industry for our cure, and they need us as the consumers.
I had the honor of chairing a panel of patient advocates who represented the changing face of advocacy. They included Kim McCleary of FasterCures, Melissa Hogan of Project Alive, and Upal Basu Roy of LUNGevity.
Each of these amazing organizations was started by patient advocates and has grown into a powerful voice on research. We discussed how people affected by chronic disease are no longer content to sit back, and how we can help advance research in partnership with industry. By including what we patients want and need early in the product and trial design, industry can accomplish its goals faster, and we can get new drugs and products sooner.
It was with great pride that I was able to share with industry representatives the fact that we now have 4,000 iConquerMS members sharing their health data to find answers to questions about life with MS. The people who come to iConquerMS do so because they trust us to do good studies with the information shared through our portal.
When I spoke at DIA, people were impressed to hear we have so many people volunteering data with no specific objectives, such as the development of a drug. There is so much more we need to learn about MS, and through iConquerMS, we are gathering the data to do just that.