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Multiple Sclerosis Society of Canada - Calgary Chapter

Nicole 
ZummachAugust 8, 2005
By Nicole Zummach

CALGARY, AB // Whether it's counselling, education, recreation programs, or advocacy, the Multiple Sclerosis Society of Canada - Calgary Chapter has been answering the call for almost fifty years. Since it was established in 1959, the Calgary chapter has grown to become the largest MS Society chapter in Canada, offering all types of support and services to people affected by multiple sclerosis. Staff and volunteers at the organization are certainly doing something right because they have been a Donner Award finalist for the past six years. They won the overall award for excellence in 2000 and received the Award for Services for People with Disabilities three times, including last year in 2004. CharityVillage spoke with executive director Mark Wolff about the chapter's role within the community, its strategic approach to program assessment, and the challenges and benefits of being part of a large, national organization.

CharityVillage: The MS Society is a very well known organization in Canada. What do you think makes your chapter stand apart?

Mark Wolff: It's a number of things. We have a strategic plan; we employ a strategic management process when we set up how we do things here. We have business and operating plans, work plans for all the staff, and everything is tied back to the strategic plan so everyone knows what they are supposed to be doing, where they fit in. And all of that is linked back to our mission, so everyone is focused on achieving the two parts of our mission: to be a leader in finding a cure for MS; and to enable those affected by MS to enhance their quality of life.

The strategic plan has been here as long as I've been here and predates me. It's just the way we do things. I think that a lot has to do with the fact that I spent 18 years in the oil and gas industry before I came here. I run the organization in a very business-like fashion. This has enabled us to be very successful from a fundraising point of view and on the services side what has really helped is that we're a big believer in program logic models, outcome measures, and indicators. That's made a huge difference as well. It's easy for people to say the work they are doing is making a difference, but if you've got a program logic model, outcome measures, and the indicators that tell you whether you are making any progress, you can prove that you are making a difference. Some people will say that what they do can't be measured. I don't believe that.

CV: How does being part of a large, recognizable organization assist you at the local level?

MW: We are the largest chapter within the MS Society, and as such, over the years we've developed some processes and tools that enable us to be self-sufficient. So we've never really had to depend on our national organization for much. Though lately they've been developing some technology-based items that we are starting to use. We have our own proprietary national database where we keep track of all our contacts. We've got a common accounting platform across the country. And we have, and always have had, graphics standards and things like that. So all of those have helped us maintain a consistent image and keep us in tune with what the national office is doing. At the same time, I think there are also challenges when you are part of a big, national organization. No matter where you go, communication is always an issue. That's no different with us.

CV: Describe some of the innovations or unique approaches that you use in the delivery of services.

MW: Well, as I mentioned, we have program logic models for everything we do in client services, and those are all based on input from our clients. We found when we were putting together the logic models for our recreation program that we had some ideas of what that program was trying to achieve. We went out and talked to the participants in the program, as well as the instructors that were leading it, and found out that their goals were entirely different than ours. They were coming for different reasons. So we changed the logic model to reflect what their wishes were.

CV: How might other organizations go about establishing logic models for their own programs?

MG: We receive funding from the United Way of Calgary and Area, so we use the United Way of America model for logic models. There are different ways of putting them together, but because we are a United Way funded agency we use their model, though they are all pretty much the same. You've got a brief narrative that explains what your program is all about and why you are doing it. Then you have inputs, some activities, some outputs, and short, medium, and long-term outcomes. In our case, the long-term outcome is always our mission. You have indicators that tell you whether or not you are making progress. Then you need some tools to gather data on those indicators. We belong to the Canadian Outcomes Institute and we use their program to input all of the data and get the reports we need.

It's a lot of work to set it up but it's an investment. Once it's in place, the value is self-evident. But if you don't buy into the concept, if you are going to fight it, then it will be really easy to say 'I don't have time to do this'. For us, it validates the things that we are doing and tells us that the things we are doing are consistent with our mission and are helping people affected by MS, that we are spending our resources wisely. It's also helping us to secure more funding. Certainly, more and more funders are demanding that you have logic models and outcome measures. I think that if you have those kinds of things in place it gives you a credibility that some other organization may not have.

CV: What do you think needs to change in terms of how people with disabilities are perceived and treated in Canada?

MW: I guess it really depends on the kind of disability that you are dealing with. MS, for many people, is a very visible disability. So people who are in a power wheelchair tend to be treated differently than someone with an invisible disability. I think that perhaps the greatest challenge is just to increase the awareness of all kinds of disabilities, the challenges people face, and some of the issues around these invisible disabilities.

CV: You've been a finalist for six of the seven years that the Donner Award has been around. What did you learn about your organization from the evaluations that the Donner Canadian Foundation provides?

MW: I find the evaluations to be very valuable. The thing I like about the Donner Awards is that they are trying to take what has traditionally been a very qualitative area and put some metrics out there so you can actually quantify how you are doing. I'm very much a numbers person, so when I get those reports I can see how we are doing against everyone else that applied and where we stand relative to them, where we are weak, and where we need to put some focus to get even better. We've been a finalist the past six years, as you mentioned, and we've won four awards. So obviously we are doing something right, but I also believe in continuous improvement; you can always do something better.

CV: What impact has winning multiple Donner Awards had on your organization?

MW: We consider the Donner Canadian Foundation Awards to be very prestigious, so we are very proud of the fact that we've received it four times. It helps with morale, recruiting staff, and retaining staff. Our peers see us as a leader, a visionary, and this just reinforces that.

For more information about the MS Society - Calgary Chapter, visit: www.mscalgary.org.

To learn more about the Donner Awards, visit: www.fraserinstitute.ca/donner/index.asp.

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