Taking Action in Olympia: WA State Action Day Recap

Yet again, MS Activists in Washington State have demonstrated that together we are stronger than MS! More than 65 activists attended our annual State Action Day at the state capitol in Olympia, and conducted nearly 100 visits to their legislators.

This year's group of MS Activists!

We brought the stories of people living with MS to our state's elected officials, ensuring they understand the needs of people with MS. Our requests focused on two pieces of legislation, HB 2326 and HB 2445, both of which will improve access to information about our health care insurance and how decisions are made about benefits and care.

Thanks to all of our activists for joining us!

MS Activist Jonathan Sari shares this recap of our annual Washington State Action Day:

MS Activists ready to take action!

On a brisk February morning, committed MS Activists from around Washington State met in Olympia to further the cause of Washingtonians living with MS.

Our legislative agenda for the session was to improve transparency in our state's health insurance system. As happened each of my prior years, we heard from expert speakers

who laid out the problems that our proposed legislation was intended to remedy, along with the outcomes we expected to result from those remedies. We also were honored to hear a vision for the future outlined by our Governor Inslee.  

Governor Jay Inslee speaks to the group.

After the presentations, it was time to speak with our legislators. For Legislative District 46, those legislators are Senator David Frockt, Representative Gerry Pollet, and Representative Jessyn Farrell. We did not manage to secure meetings with Representative Pollet or Senator Frockt, but Representative Farrell graciously made time to meet with us.

It was my third year attending our State Action Day. This year, my two compatriots (who had made the hour-long drive from our North Seattle district to the state capitol each of my prior two years) couldn't attend -- so I conducted the visits on my own.

Jonathan Sari (right) at a legislative meeting last year

I arrived at Representative Farrell's office fifteen minutes early. These legislators are busy! While I waited I watched her wrap up a meeting with the fire fighters union and receive a message from the Speaker of the House -- a request that ended up limiting our meeting time. 

Representative Farrell remembered me from our earlier meetings and given our limited time, I kept our request to the basics: I asked for her support for our bills and explained that we hoped to streamline reporting and improve accountability for health insurance. She asked some good questions and although I didn't remember all of the specific answers, I promised to get answers that day. I also shared my personal experience of my own medication denial by my insurance company. I thanked her for her time, letting her know that I was following her email newsletter, and let her get to her meeting.

MS Activists meet with legislative staff.

I also dropped off the information packets with Representative Pollet's and Senator Frockt's offices. Before returning home, I reported in to Linnea, the Chapter's advocacy manager, to request the information to follow up so I could follow up that evening with Rep. Farrell.

I am glad to be a part of the Society's efforts to make government work better for those of us living with MS.

-Jonathan Sari

Visit our Facebook page for more photos of our State Action Day event.

Questions? Want to get involved? Let us know.

Success in Olympia: State Action Day Recap

Another successful State Action Day has come and gone, and what a day it was! MS Activists came from all corners of the state -- as far as Spokane, Granite Falls, and Vancouver -- to be a part of the event. 

Here’s a recap of what MS Activists were up to on January 27, 2015: 

• More than 40 MS activists came together in Olympia to show their support for people living with MS and conducted over 75 in-person visits with lawmakers
• At home, activists spread the word via social media and sent more than 80 messages to their legislators 

Together, we successfully raised awareness and made a powerful ask for increased funding for special needs transportation -- services that help people with disabilities get where they need to go. Access to transportation is a major issue for people living with MS. Mobility impairments and fatigue are some of the most common symptoms of MS, and as the disease progresses, many individuals are no longer able to drive.

People with MS and other mobility challenges need and deserve the opportunity to access jobs, shopping, church, and community activities, so they can live as full a life as possible. Washington’s lawmakers have the ability to improve the lives of people with MS by increasing funds for special needs transportation. 

Rep. Linda Kochmar (left) with MS Activist Cermit Rickey (center).

The special needs transportation fund breaks down barriers to transportation for people who are unable to drive because of a disability or age. It funds projects that help local communities offer efficient, coordinated transportation services, such as paratransit or non-profit transportation programs. While paratransit programs are required under federal law, local transit agencies often have a difficult time funding them. 

We can do better—and that’s where we need your help! MS activists are working together to ensure that our state provides adequate funding for accessible transportation. We asked lawmakers to support an additional $160 million in special needs transportation funding in the next transportation package. This ask resonated with many legislators who continue to express their support for this request.

Commissioner Mike Kreidler speaks to the group.

Finally, we were honored to host special guests Insurance Commissioner Mike Kreidler and Senator Joe Fain. Commissioner Kreidler spoke to the group about critical insurance issues affecting the MS community, including increasing transparency in prescription drug formularies and improving provider networks. Senator Fain energized the room with his overview of key transportation issues and the value of constituent voices in moving issues forward.

Thank you to all of our activists for raising awareness and speaking up on behalf of the MS community. If you weren't able to attend, you can still make a difference! Email your legislators today and ask them to fund accessible transportation. 

Questions? Want to get involved? Let us know.

Join MS Activists in Olympia next week!

State Action Day is just around the corner. This annual event brings together MS Activists from all over Washington to raise awareness of issues affecting the MS community among our state legislators. If you are new to advocacy, but still want to attend -- don't worry! We will provide ample information before and during the event to get you up to speed. 

Our elected officials want to hear what matters to their constituents. Together, we will bring them the stories of people living with MS and we help change laws. Still not convinced? Here's some of the reasons you should attend State Action Day:

1. To build a relationship with your legislator. If you already have one, consider it a visit to a friend. Your legislator represents YOU and wants to hear about issues relevant to your life.
2. To stand in solidarity as an MS community, to speak out on behalf of all the 12,000 people living with MS and the 72,000 people in our state affected by MS 
3. To make a statement. As our state legislators make decisions, we want them to keep the needs of people of MS in mind. We will help them understand what issues matter to our community. 
4. To make a difference. Together, four years ago, we passed a law that allows more MS specialists to practice in our state. Three years ago, we stopped people with MS from losing their health care. Two years ago, we made sure everyone with MS has access to affordable and comprehensive health care. Last year and this year, we are continuing our work to support accessible transportation options to help people with MS get where they need to go. Help us make change.
5. To build awareness. Our presence at the Capitol (in our orange scarves) brings attention to our cause! It also educates you on current issues that you can share with others who care about the MS community.

I hope you can join me and other MS activists in Olympia on Tuesday, January 27th to share important issues affecting the MS community with our legislators. 

Registration is still open! 
Sign up at www.nationalmssociety.org/WAactionday 
or by calling 1-800-344-4867, option 1.