About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

Thank You, Maybe

By Lauren Kovacs

I admit this is a tough emotion for many MS folks. I am not exactly the “glass is half full,” sparkles, and glitter type. Not sure how I survived as a college cheerleader. Many were bubbly, barf. I was more of the stick in the mud with a giant white bow.

Gratefulness has been a learned trait. I force myself to see the green grass and pretty unicorns. I often see giant animals pooping on my lawn with sharp pointy things on their heads. Many of us have to really try to be thankful. Come on! MS has taken a lot and it is not a generous disease.

Alas, finding thankfulness is hard, but we must try. I would fit in well with a Grinch family, however green is not my color. See, glass half empty!

I have to “cheer” myself on just to get to the bathroom in time.  Finding things to be grateful for takes on a new identity. If I manage to tie my shoe or put elastic in my hair on the first try, I celebrate it.

Small things deserve great thanks. MS folks adapt better than most. I am a lefty, yet I have learned to apply eyeliner with my right hand. I drove my figure skating instructor nuts because I spun like a lefty and jumped like a righty. In kindergarten, I cut paper right but, wrote left. Drove my teacher crazy enough to put me in some special ed. classes. Little did I know that one day this ambidextrous trait would come in handy. That is something to be very thankful for.  I still can’t write right handed, yet every other thing I can do with my right hand.

I learn to be thankful for much smaller things. Simple stuff does matter. Think about just getting through the day. Toilet paper, straws, walkers, naps and all that meaningless stuff is, in fact, deserving of our thanks.

I am thankful my boys can enjoy gluten. Stuffing at Thanksgiving would suck. I am grateful I have enough self-control to resist it. Talk about resisting temptation.

MS reveals how tiny stuff can induce great thanks. I am very thankful for anti-bacterial wipes. I can de-germ my walker and wheelchair wheels pretty easily. Think about where they go. When I did horseback riding therapy, those wheels went over horse poop.

Even though I have had to give up my jeans, being small enough to wear fun kid-size leggings is a trade off. Yes, I have lots of sneakers too, but less of an ankle injury risk than heels. I am truly thankful for that.

It may take some thought, but we can find stuff to be grateful for. It might seem simple to some. I get weird looks for being thankful for my piggy dog, but he cleans up all the food I drop on the floor. He is now on a diet though. Poor guy. He loves food.

I am thankful for having a life jacket. Drowning in my own pool was not on my bucket list. Small things to be grateful for shows humility. It can be fun, too.  I love that I can paint my own nails, if I use glitter polish. Covers the mess well.

When going around the table talking about what you are thankful for, think. Small things show that you have character. It might make someone else see how blessings come in all sizes. I personally, am grateful for whoever invented elastics for pants. Sweet tea is a close second. Electric toothbrushes are a lifesaver, too. No swamp mouth.

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Being Grateful: Validate the Hardship and Strive for the Bronze

By Stacie Prada

I used to think being positive meant focusing only on the good things in life.  I was really good at it too. A friend would say she’d had something bad happen, and I wouldn’t miss a beat to respond with how great it is that a worse outcome didn’t result.

I did it with myself too.  It seemed like if I let myself think about the difficult things, that it was being negative. That it could lead falling into a dark place of feeling bad and never climbing out.  I once had a counselor tell me after 9/11 that thinking about what happened doesn’t make you sad. What happened makes you sad.

In that way, thinking about having multiple sclerosis doesn’t make me sad. My chronic illness and progressing MS symptoms make me sad.  Ignoring them doesn’t change the fact that I have both. We’re not limited to feeling one emotion at a time, and feeling sadness or frustration with one aspect of life doesn’t preclude feeling optimistic.  I’d argue that we need to feel one to appreciate the other.

To feel genuine gratitude, I need to know it’s not mandatory to stuff my feelings and be happy every moment. I can’t ignore the tough parts of my life and only acknowledge the things that make me grateful. I can’t just write a list of unrelated things to be thankful for and stay sane. If I’m feeling sad or resentful, I need validation that it’s understandable to have those feelings. If I skip this step, I’m minimizing my frustration or implying I don’t have a reason to feel bad. Once I sit with it, grieve for it, and assure myself I’m not weak or overreacting, I can then choose to focus on things that make me grateful. Sometimes it’s a quick shift, other times it’s a rough climb out of funk. Either way, it helps me come to a place of genuine appreciation in my life.

I think about it as winning a bronze medal. There’s an article in Scientific American, Why Bronze Medalists Are Happier Than Silver Winners, that I think we can use in our own lives to be happier.  People who compete and miss winning first place exhibit less happiness than people who don’t perform as well but still make it to the podium. Silver winners focus on the one person who did better.  Bronze winners compare their performance to all the people that tried and didn’t win anything.

When I’m grateful, I’m recognizing my efforts and satisfaction. I’m not seeking perfection.  I’m looking at how amazing things already are.  I may acknowledge what could be better, but I’m recognizing all the ways it could be worse. Some people seem to have a point of pride of noticing the error or the flaw in things. They can make you feel like you’re never good enough. Try not to judge yourself harshly and add to feeling miserable.

How we perceive our situation makes all the difference. When living with a progressively disabling chronic illness, things will stink and be sad and frustrating and feel too big to deal with at times. Sometimes the best I can do is know that how I feel right now won’t last forever.

The measure of success changes depending on my health.  If I can participate in a race and come in last, I’m grateful that given my circumstances I can do it at all. If I feel bad, I know that’s a part of the condition and grateful for the abilities I still have.  If I’m experiencing a permanent loss, I acknowledge that it’s sad to experience the loss and grateful for the time before the loss.

Strive to have a mindset of someone who’s coming in third.  Or someone who’s in last place and may or may not finish. You’re still doing it.

*Stacie Prada was diagnosed with RRMS in 2008 at the age of 38.  Her blog, “Keep Doing What You’re Doing” is a compilation of inspiration, exploration, and practical tips for living with Multiple Sclerosis while living a full, productive, and healthy life with a positive perspective. It includes musings on things that help her adapt, cope and rejoice in this adventure on earth. Please visit her at http://stacieprada.blogspot.com/ 

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Meet the Board

MSAA strives to be a leading resource for the MS community by improving lives today through vital services and support – and we could not accomplish this without the help of our volunteer board members.  MSAA’s Board of Directors is comprised of accomplished professionals from across the country who volunteer their time to further MSAA’s mission.  With our new series, Meet the Board, we hope to introduce you to our wonderful volunteer board members!

MSAA is proud to highlight two volunteer board members this month – Jennifer L. Schwartz, Esq. and Barry Singer, MD!

Jennifer L. Schwartz
Chair of the Programs and Services Board Committee

Professional Background: Jennifer L. Schwartz, Esq. of Philadelphia is the Vice President of Legal Affairs & General Counsel for Lourdes Health System (LHS) and St. Francis Medical Center (SFMC). She was initially hired by LHS as its first in-house attorney, and after just three years as the Assistant Vice President, Legal Affairs, was elevated to LHS’ chief legal officer as a direct result of her foresight, strategy initiatives and legal expertise.

Barry Singer
Executive Committee Member, Chair of the Development Committee, and member of MSAA’s Healthcare Advisory Council

Professional Background: Barry Singer, MD of St. Louis is an expert MS neurologist and has been the Director of The MS Center for Innovations in Care at Missouri Baptist Medical Center since 2008. He is an Assistant Professor of Clinical Neurology at Washington University School of Medicine since 1999 and maintains privileges at Barnes-Jewish Hospital. He has been an investigator in greater than 25 multiple sclerosis trials (Phases I to III) focused on new therapeutic options. He continues to publish peer-reviewed articles, present posters and lecture globally on multiple sclerosis.


What inspired you to join MSAA’s Board of Directors?

Schwartz: “I had been looking for a non-profit Board to join and give back to the community when, coincidentally, a current MSAA Board member contacted me and asked if I would consider joining the MSAA Board. I was blown away because just a week earlier my Dad’s twin sister had passed away from complications associated with progressive MS. She was never able to benefit from medications and relied heavily on help from others – a specialty of MSAA. One of my best friends from college also has MS. I felt that it was meant to be and that by taking on a Board position and giving it my full dedication I would be honoring my Aunt and accomplishing my ultimate goal of giving back to others through the MS community.”

Singer: “For over 15 years, I have collaborated with the MSAA on important patient educational programs nationally. My goals align with the MSAA’s deep commitment to trying to help people living with multiple sclerosis receive the resources they need to live as well as possible. For example, MSAA funds MRI scans for patients that could not afford the test which has often led to important medical decisions. Joining the Board allows me to make a positive difference on the lives of those living with MS.”

What are your goals as an MSAA Board Member?

Schwartz: “I want to contribute new ideas to the future strategic goals of MSAA. I hope to be an excellent representative for MSAA and to assist the organization in enhancing its impact across the world. It is also my goal to motivate other people and organizations to contribute to MSAA. These are my obligations to the clients served MSAA and to the amazing and dedicated staff of MSAA.”

Singer: “As a multiple sclerosis specialist on the Board, I provide a unique voice due to my insight into the desires and needs of those living with MS. I have been able to advocate for programs that will have greatest impact. In addition, I frequently provide recommendations on the MSAA’s position on rapidly changing healthcare news. As a board member, I’ve been involved with the MSAA’s national and international leadership on communication between patients and their healthcare providers. As a Board Executive Committee member and head of the Development Committee, my goal is also to develop the relationships that ultimately fund these critical resources for those living with MS.”


Editor’s Note: MSAA is extremely proud and honored to enlist the support of Ms. Schwartz, Dr. Singer, and all of our dedicated Board Members who volunteer their time, expertise, compassion, and leadership to help us achieve our mission of improving lives today for the entire MS community. We are very grateful for their service and look forward to their continued support as we strive to serve more people in more places than ever before. Thank you once again Jennifer and Barry!

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Advocacy and the MS Community

By Kyle Pinion

When one thinks about advocacy especially in this very heated political climate, there are certainly some tough connotations that have be dealt with, particularly in regards to the concept of lobbying. But in truth, the concept of advocacy does not have a political slant, and in the world of non-profits it is simply the act of representing the needs of people who do not have a voice within the halls of the US Capitol. MSAA, as a member of the broader MS Coalition, is proud to be an advocate for people with MS, and in turn an advocate for the greater disability and chronic disease community. Year in and year out, working with our partnering organizations within the MS Coalition, we sit down with members of Congress and their healthcare staffers to discuss issues of importance to the MS population. Some of these topics may include MS research funding, or enhancing the federal government’s commitment to understanding the true incidence and prevalence of MS within the United States, or matters related to easier access to durable medical equipment (DME). These are just broad examples, but they give you a sense of how wide-ranging some of these national efforts are.

But MSAA’s advocacy work doesn’t stop there. We also are actively engaged in issues at the state level. Utilizing local thought leaders, medical professionals, those living with the disease and other coalition partners, we advocate for the needs of the MS population in all fifty states where barriers and inequity may exist. For example, if an issue arises where an insurance provider may not allow for open access for all MS therapies, that is an area in which we would commonly take action. Another instance may be the availability of rehabilitative physical therapy for people with Primary-Progressive or Secondary-Progressive MS. if it impacts the MS community and can be addressed at the federal, state, or local level, MSAA is proud to take action and work with our partners to seek solutions for these issues with both elected and private entities.

In addition to our work “behind the scenes”, our organization also seeks to educate individuals living with MS and their family members about how to best advocate for themselves and the community they are a part of. Self-advocacy is one of the most powerful tools available to the MS patient, and it’s our goal to inform our clients about the strength of the individual voice when speaking on issues of importance. Your elected officials want to hear from you, and while they value my and my colleagues’ time when we visit their offices, the truth is you are their constituent and your experience as a constituent within the district they represent means even more. No matter what you’re able to do – be it an email, a phone call, or even the all-important in-person visit – that sort of self-advocacy not only benefits you, but it also allows you to represent all of the people with MS that cannot be in that room. And therein lies some really incredible power. In that way, your voice really can turn the tide.

Don’t be afraid to get started, and let us know how we can help. It’s what we’re here for.

*Kyle Pinion is the Director of Public Policy and Advocacy, as well as the Southeast Regional Director for the Multiple Sclerosis Association of America. Before coming to MSAA, Kyle was the Director of Public Policy and Advocacy for the National MS Society – Georgia Chapter where he acted as the chief lobbyist for the chapter in the Georgia State Legislature, and their staff representative with the US Congress.

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Insurance Resources

Dealing with insurance of any kind can be a stressful experience for anyone if you aren’t familiar with the language and jargon used on the forms.  Health insurance is no different – particularly when you are trying to make sure that the health insurance you have covers all of your health needs, including any regular therapies, durable medical equipment, specialist visits, and regular tests.

Navigating the world of health insurance can be daunting, but our Client Services team here at MSAA has a couple of resources that can help get you started on resolving your questions and issues:

  • Patient Advocate Foundation – The PAF provides case management for patients who are dealing with insurance, employment, or other legal issues related to their medical condition.
  • State Insurance Departments – This link will take you to a map of the United States with a link to each individual state’s insurance web page that can offer more information about the insurance laws and the insurance marketplaces available in your home state.
  • Life Happens – This non-profit provides information and resources to find life insurance, disability, and long-term care insurance policies/plans, and they can help you find a local agent to assist you with those plans.

You can also visit the main website for Medicare and Medicaid to find additional information about these two government-funded health insurance options.

This is just a short list of resources that you have at your disposal to help you work your way through your insurance questions.  For more information about your particular question or issue, please feel free to reach out to our Client Services Specialists at (800) 532-7667, ext. 154 or at MSquestions@mymsaa.org.

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Never Stop Asking Questions

By Penelope Conway

Making my way through the medical insurance nightmare has been a challenge since being diagnosed with multiple sclerosis. It wasn’t something I thought much about before MS came along. I never really got sick so health insurance and my own well-being just wasn’t a priority. Talk about a learning curve. I was thrown into things head first and then bounced around a few times before landing hard with a thud.

My life was suddenly filled with doctor appointments, medications, unpredictable symptoms and massive medical bills. I found myself in this new world of the chronically ill and I didn’t like it one bit. To be honest with you, it scared me more than anything I had ever been through.

I think the first year after I was diagnosed, I spent much of my days in a mind numbing fog. I became overwhelmed with the vast amounts of information I found online about MS and the high costs associated with it. The more questions I asked, the more questions I had.

I became more concerned with being able to afford my co-pays and medical insurance premiums than with the latest phone apps or music downloads. I found myself searching for insurance plans that made MRI’s and durable medical equipment more affordable. I researched Medicare, SSDI and early retirement. I looked for ways to afford home modifications and accessibility aids.

I discovered that no one can look out for me better than me.

When I was searching for a supplemental insurance plan that would cover all the things Medicare doesn’t, the monthly cost was too high for me to be able to afford. So, what did I do? I got online and through asking tons of questions came across a foundation that helps people with MS pay their monthly insurance premiums. That was something I would have never known about if I didn’t dig around for answers myself.

I found that asking questions is the best thing anyone can do for themselves.

When the cost of my pain medication went up, again I got online and found that my Medicare drug plan had an exception form that can be submitted to request a lower co-pay. I had my doctor help me fill it out, sent it in and the cost of that one medication went from $45 a month to $3. The insurance company won’t tell you about that option in bold print on their home page. It’s something you have to ask questions about and search for yourself to find.

Then there was the time a few years ago when my powerchair was damaged in a car accident. I was okay but my chair got banged up a bit. I discovered that my homeowners insurance covers things like that. I was able to get a new chair to replace the broken one. Who knew homeowners insurance (or renters insurance) worked that way? I sure didn’t. Another lesson learned by again asking lots and lots of questions.

I don’t think I will ever understand insurance or how they calculate the costs associated with their services, but through asking tons of questions and digging around for answers I have been able to ease much of the costs associated with MS and living with a disability.

You have to be your own advocate, do your own research and never stop asking questions! You may not be able to control the progression of your MS but that should never stop you from taking control of your own health care.

*Penelope Conway was diagnosed with Multiple Sclerosis in November 2011. She is the author and founder of Positive Living with MS (positivelivingwithms.com) where she uses humor and her own life experiences with MS to help others navigate this unpredictable journey. She believes that staying positive and holding onto hope is the key to waking up each morning with the strength to get through the day.

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Dealing with Insurance Denials

By Stacie Prada

Over the years I’ve appealed a lot of health insurance denials for different reasons.  I’ve dealt with getting denied for claims, denied for policy coverage, and denied for pre-approval for certain treatments. Each time I open the denial paperwork, I can literally feel my blood pressure go up. Now I have something to deal with on top of everything else.

I didn’t learn how to deal with these things in school. Yes, I learned to read, understand text and problem solve, but insurance paperwork is formal, in small print, and not always clear.  Getting denied creates an emotional response with financial consequences.  I see people shut down when they need to read legal paperwork, and I’m saddened when it costs them money they didn’t need to spend.  I’ve learned what to do by dealing with each denial one at a time. Thankfully so far, my experiences have been what I’d think of as the minor league level of insurance appeals where I was able to do them myself.

I’ve had to prove I’m not divorced or legally separated to continue coverage for my spouse. While we were in the process of getting divorced, I legally changed my name to my maiden name and gave them the judge’s order showing the name change.  My insurance company wanted proof I wasn’t divorced.  I was angry and completely stumped.  How do I prove I’m not divorced?  There’s not a judge’s document that shows a person is still married.  By talking to insurance representatives, they finally were able to tell me what kind of documents would satisfy them.  I had to provide them with our marriage certificate, my name change order (again), joint bank statements with the address they had for us, utility bills with both our names, and federal tax returns to show we were still filing as married. It took all of that plus a lot of effort on my part and time on theirs before they continued covering my spouse and re-processed his claims.

I had a provider that would bill the insurance provider and would receive no response EVERY time. We finally learned the routine. First, my provider would let me know the claim hadn’t been processed for a long time. I would then call the insurance company to ask about it, and the person on the phone would tell me it was in process and should be paid within the next week.  While absurd and seemingly a tactic used to avoid paying, I accepted it as part of the process with that company and my provider.

I’ve formally appealed my insurance company’s refusal to cover my disease modifying medication at a dosage of three days per week. I knew the daily dosage worked for me, but I couldn’t find seven different areas on my body to do injections each week without body tissue breaking down. I tried two other medications and lived with terrible side effects for over a year hoping they would subside without success. While appealing the insurance company’s denial, I lived without any disease modifying drug for six months.  It was stressful going without something that has been proven to slow progression of MS.  Not knowing if it would get approved or how long it would take compounded the anxiety the process caused me.  I wish it had occurred to me to look online for examples of appeal letters.  While mine was effective, it took me a while to write and was stressful worrying that it wouldn’t be successful.

I’ve had bills come through that have been denied because the provider billed the wrong insurance company. Just the most recent bill would have cost me $750 out of pocket if I hadn’t been paying attention.  It astounds me to think of all the money people are paying that they shouldn’t.  All because it looks like every step has been done and they’re told the remainder is their responsibility.

I know people who think that yelling at the company helps. Personally, I think yelling at the customer service representative is a waste of time. That person didn’t create our insurance system and isn’t the one creating policy at the company causing your frustration.  I think the people answering phones are just following orders and trying to keep their job to support themselves and their family.  Letting them know you’re frustrated is useful. Yelling and not listening increases the amount of time it takes to figure out what the issue is and what will help. It adds to my stress level and makes my life harder.  Advocating for my care doesn’t need to feel like a battle.  By being friendly, I’ve had pleasant interactions with insurance representatives that have brightened my day.

What I think helps me navigate insurance appeals:

  1. If you don’t understand the denial, call the insurance company and ask them to tell you what the reason was and what you need to do for them to approve or re-process the claim.
  2. Be pleasant to the person on the phone. If I’m upset, I’ll tell them, “I know this isn’t your fault. I’m really frustrated, so please bear with me.” I can hear the person on the phone relax, and it seems they’re more willing to help problem solve my issue.
  3. Accept that often you’ll need to provide things repeatedly. Sometimes it’ll be each time a claim is processed, others will be annually.
  4. Maintain good records of medical bills and payments. See my blog post for tracking medical bills if you want tips or a system: Creating Some Order In The Medical Billing Chaos.  If you haven’t kept good records, just call your insurance company and your medical provider to figure out what the status is and what you can do now.
  5. Open all medical bills or insurance statements when received to see what they say. It’s tempting to put bills and other mail in a pile for later, but that’s a habit that makes it easy to lose track of paper and time. Waiting will only compound some issues and leave you with less time to resolve them.  If it says it’s covered, you’ll know how much you owe. This may shape decisions you make regarding purchases.  And sometimes it’s good news!
  6. Keep copies of documents with medical insurance files so that you know what was provided in the past. It will also be ready to send again when they repeatedly deny coverage for the same issue.
  7. If feeling the tendency to shut down, take a break. A few minutes or days may be needed to be able to work on it again. Usually appeal deadlines I’ve seen are 180 days.  Know the timeline, and don’t wait until the end. Otherwise you’ll keep getting bills that can hang over you and cause anxiety.
  8. Share your experience with friends or coworkers on dealing with medical appeals. They often have experiences of their own with advice that may help you in your situation.  You may also be helping them be better prepared for dealing with their own insurance issues.
  9. For writing appeal letters, look online for examples. I searched for “prescription appeal letter,” and found many terrific examples to follow.  If you enter the specific name of the medication or device you’re trying to obtain with “appeal letter” you’ll find lots of tailored examples. If there isn’t one specific to your situation, use the others as a guide for how to convince your insurance company to approve it.
  10. Remember you don’t always have to figure out everything on your own. Look for your resources.  There are online suggestions from organizations about dealing with insurance.  Friends and family can often break down the issue to a level that’s manageable. If the stakes are really high, you may want to get professional assistance with your appeal.

Having a chronic condition that requires ongoing medical treatment is already frustrating and draining.  Learning how to navigate the insurance world and cultivating the patience needed to deal with it goes a long way. It can improve your medical care, reduce out of pocket expenses, and make life a lot easier than it might be otherwise.

*Stacie Prada was diagnosed with RRMS in 2008 at the age of 38.  Her blog, “Keep Doing What You’re Doing” is a compilation of inspiration, exploration, and practical tips for living with Multiple Sclerosis while living a full, productive, and healthy life with a positive perspective. It includes musings on things that help her adapt, cope and rejoice in this adventure on earth. Please visit her at http://stacieprada.blogspot.com/

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Make Your Web Browser More Reader-Friendly

Visual disorders affect more than half of all individuals with MS, which can make even simple tasks more difficult.  Everyday things take more effort and more time when your vision is impaired in some way, including reading or doing anything online.  In this day and age, almost everything can, or needs to be done online, making surfing the internet unavoidable.  While many websites make an effort to be visually interesting and engaging, as well as readable, it can still be a challenge to read the information on your computer screen.

Every web browser is different, but there are some tricks that you can use to make your online experience a little easier when looking for information on the internet:

  • Font Size – If the type on a web page is too small, easily zoom in to make the font larger by pressing the “Control” key (on a Windows computer) or the “Command” key (on a Mac computer) and the “+” key. To zoom back out, press the “Control” or “Command” key and the “-“ key.
  • Clickable Content – An easy way to navigate around a page to find a link you are looking for is to hit the “Tab” key on your keyboard while on a web page. This will start where you are on the page and highlight the first link within view. To move further down the page, keep hitting the “Tab” key until the link you wish to click is highlighted. If you accidentally go past the link you wanted to click, press and hold the “Shift” key then press the “Tab” key to go backwards up the page. Press the “Return” or “Enter” key to click a highlighted link.
  • Cluttered Page – Most web browsers also offer the option of a “Reader Mode” which will remove ads, leaving only larger text and associated images, making the page easily readable. Web browsers that offer this mode include: Chrome, Microsoft Edge, Mozilla Firefox, and Safari. These extensions or settings may not work on every web page, but they can make the overall online experience a little easier.

For more details on how to adapt your browser to meet your accessibility needs, visit the browser-specific links below:

What tips, tricks, and tools do you use to improve the appearance of what you are reading online?

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Stories to Inspire

By Kaitlyn Gallagher

On a lovely weekend in mid-September, the Rock ‘n’ Roll Marathon Series took over Philadelphia’s Benjamin Franklin Parkway with thousands of dedicated runners. Whether participating in the 5K, 10K, or half marathon, runners represented countless nonprofit organizations with colorful shirts, logos, and team “swag” to raise awareness for their particular cause. I was lucky enough to represent #TeamMSAA as a runner in the Rock ‘n’ Roll 5K along with a few others, including another MSAA employee, Emily!

I felt a bit out of my element running in a large scale race that Saturday morning – I’m certainly no athlete and even spent a few weeks training leading up to the race to make sure I was prepared! However, there was one runner on #TeamMSAA that was no stranger to racing for a cause. John Derry Jr., our top fundraiser for the Rock ‘n’ Roll Series in Philadelphia, has run many times in support of different organizations. This year, John discovered that he could run in support of the MS community, and knew that he had to sign up for a very personal reason.

“MS has had a great impact on my life due to my grandmother having MS. My grandmother has shaped the man I am today,” said John. “I have been taking care of her my entire life. I am currently her primary caretaker. Over the years of caretaking I have grown to learn how to take care of others and pay attention to other’s needs.”

Meeting John was an incredible experience – he is a truly selfless person who not only takes on the responsibilities of caring for his grandmother, but spends his free time training and running to help others living with MS. He has taken his passion for running and turned it into a mission to serve others, and for that MSAA is extremely thankful! John raised over 700 dollars that will go toward providing members of the MS community with free programs and services like cooling vests, mobility equipment, MRI funding, and more.

John plans to continue running in other races, and is currently applying to get his Master’s degree to become a Physician’s Assistant, another decision influenced by his years as a caretaker. We wish John the best of luck in all of his future endeavors, and thank him on behalf of the MS community for his amazing work as a caretaker and advocate!

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MSAA Publishes New Booklet About MS Progression

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We here at MSAA are pleased to announce another new publication, Understanding Progression in MS. This valuable resource is designed to help people with MS and their loved ones better understand what is happening when progression in MS occurs and provides a number of treatment options – from the newest approved disease-modifying therapy to symptom management and wellness strategies.

Understanding Progression in MS includes:

  • An overview of the background information and details of the types of MS
  • An overview of how progression in MS is thought to develop and how it is evaluated
  • Current treatment options, noting specifically how treating inflammation differs from treating progression
  • Detailed information on several prominent symptoms and symptom management
  • Strategies for healthy living with progressive MS

Check out this latest publication and view or order your copy today!

 

Funding for Understanding Progression in MS was made possible by Sanofi Genzyme.

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