MS Awareness Month: Creating an Inclusive and Compassionate Society

As an advocate, I speak to people in the MS community every day. We chat about our disease and what it's like living with it. One wish I often hear is for the able-bodied community to better understand what it's like to live with MS.

In honor of Multiple Sclerosis Awareness Month, I'll shed a little light on what it's like to walk in our shoes.  

MS 

I don’t know about you, but I think of my life in terms of chapters, except my chapters aren't arranged in numerical order. Instead, they're divided into two categories, before and after diagnosis.

Before my MS diagnosis, I could ride a bicycle for miles and miles. In the summer I'd play softball, basketball, or kick-the-can from morning until sundown. When my husband, a devoted tennis player, and I were dating he'd give me tennis lessons. Of course, he beat the pants off me, but we always had fun.

MS

Looking back I didn't realize what magical days those were.

It’s been a long time since I could run, ride a bike, or walk endlessly.  I miss those bygone days.

MS

2014. I always felt so free on my bike.

No matter what "type" of MS you live with life is constantly a challenge.  After losing any ability, such as walking, your days can be frustrating, maddening, and completely heartbreaking.

In time, some people can learn to live with their new normal while others can't. It's a tricky road we travel. MS

Over the years I've made a conscious effort to hold Jon Kabat-Zinn's quote close to my heart:

"There's always more right with you than wrong."

It sounds trite but it works for me to keep that beautiful sentiment in mind.

Zinn's wisdom gives me hope for better days ahead.  MS

The way I figure it, no one escapes this life without facing some sort of adversity. MS was simply the hand I was dealt.

There are better days than others but when they're tough I've learned to meditate and focus on what I still can do.

I can work. I can speak. I can walk. I can swim. I can drive. I can stand. I can talk. I can laugh. I can dress. I can write. I can think.

And I can feel grateful for all of these blessings.    

MS

I want you to know that whenever you see me you're seeing the best possible version of me. I rest when my body tells me to, which is quite often, and I can safely say that most people in the MS community do the same.

MS

Some of us choose to take medications specifically designed for our MS (called disease-modifying therapies) to hopefully put the kibosh on disease progression. Some work for us, and some don't.

We're called the "snowflake disease" because no two people have MS alike, and none of us react to medications in the same way.

We can feel okay one day (or days) and lousy the next day (or days).  It's a very fickle disease!

Symptoms of MS can include pain, bladder, bowel and cognitive dysfunction, vertigo, weakness, numbness, optic neuritis, insomnia, dizziness, spasticity, fatigue, depression, and anxiety.

And the comorbidities that often accompany our MS diagnosis, such as various autoimmune diseases, gastrointestinal diseases, vascular and cerebrovascular diseases, chronic lung disease, and vision problems.

Instead of seeing us as an extension of our disease, I hope you'll look at us for who we are. We are made of beautiful hearts, souls, and minds.

We're so much more than what meets the eye. 

MS

A bunch of MS advocates hanging out and having fun together! I love our community.

Thanks for listening and for taking positive steps toward creating a kinder, more inclusive, and compassionate world for everyone.

MS

NOTE: Click MS RESOURCES at the top of this page to learn more about MS. Thank YOU

Aging with MS and How YOU Can Manage Your Journey

When my neurologist diagnosed my MS over three decades ago my parents urged me to get a second opinion. I agreed wholeheartedly.

The second neurologist, who came highly recommended, quickly confirmed the diagnosis, then casually added:

"On average people with MS live seven years less than the general population.

I thought my head would explode...from the diagnosis, the doctor's (ahem) bedside manner, and the mic drop about MS and mortality. Jeez.

aging with MS

With limited information at my disposal in those pre-internet days, I was desperate to research credible information to validate (or invalidate) the doctor's opinions as well as the many other "truths" people felt compelled to tell me.

Knowledge and self-advocacy are power.

I made a pact in those early days to educate myself and those in the MS community with absolute truths about the disease.

We deserve nothing less. 

So here's part two of my series on AGING AND MS. (In case you missed part one please click here.)

I'm sharing another leading resource I rely on for outstanding support and services.

The Multiple Sclerosis Association of America

Since 1970 this nonprofit organization has lived up to its tagline "improving lives today."

I highly recommend perusing their website to learn more about what MSAA can do for YOU.

aging with MS

Over the years I've gotten to know the President and CEO of MSAA, Gina Murdoch. Leading with compassion and commitment to the MS community, Gina graciously agreed to answer a few questions about aging and MS.  

WAIT! STOP!

aging with MS

Don't turn away because you think, "I'm not 50 yet so this doesn't apply to me."

It certainly does. If not today then someday. Do yourself a favor and keep reading. Some of the links below might even help you RIGHT NOW.

I promise it's worth your time to keep reading.

aging with MS

Let's begin with a quote from Gina Murdoch about aging and MS:

"The MS journey has many challenges and aging with MS is certainly one of them."

Cathy: How has MSAA included the over 50 demographic?

Gina: All of MSAA's programs, core services, and initiatives are available to help those living with MS wherever they are on their MS journey. MSAA's programs and services are inclusive of those living with MS over the age of 50, and specifically include:

MSAA's Helpline:

MSAA provides a toll-free Helpline and Chat that enables individuals with MS, family members, care partners, and friends to speak directly with one of MSAA's experienced specialists. MSAA's Helpline routinely assists those seeking help on topics related to aging and MS.

MSAA's Equipment & Cooling Distribution Programs:

MSAA's Equipment & Cooling Distribution Programs offer products for individuals who need cooling equipment or devices designed to improve safety, mobility, exercise, and daily living capacity.

MSAA MRI Access Program:

The MRI Access Program assists with the payment of cranial (brain) and c-spine MRI scans for qualified individuals who have no medical insurance or cannot afford their insurance costs and require an MRI to evaluate current MS disease progression.

MSAA's Educational Resources:

MSAA's educational programs cover an array of topics featuring leading MS healthcare professionals and include issues that impact individuals living with MS over the age of 50.

Some recent highlights that specifically address aging with MS include:

* * Community Views: Aging Fears with MS (a blog post by MultipleSclerosis.net posted on MSAA's MS Conversations blog - 3/30/2022)

** Ask the Expert - MRI, and MS (4/29/2022)

Dr. Barry Hendin answers questions from the MS community and refers to the need for MRIs as MS patient ages.

** Playing the Cards I'm Dealt (3/14/2022)

Blogger Stacie Prada discusses a look back on her diagnosis and life since that pivotal point in time.

**Ask the Doctor: Questions from our readers

Dr. Hendin addresses age-related questions from the MS community.

Ongoing and future initiatives:

MSAA is currently partnering on research and educational initiatives relating to menopause and MS and is looking to address the issue of aging with MS in a future issue of The Motivator magazine.

My thanks to Gina Murdoch and MSAA for the very fine work they do for our community.

NOTE: Since I mentioned MS and longevity at the start of this post here's some information I gathered for you on the subject. I know this isn't the happiest of topics but please keep in mind that statistics can't possibly measure our unique MS situations. Be sure to check out the links below to Gavin Giovanonni's and Dr. Hendin's articles:

I hope you enjoyed this post. Please feel free to leave any comments or questions below. I truly enjoy hearing from you! 

When Beauty and the Beast Collide

The BEAST that's lived in my body for more than half of my life started to erupt over the last few years in unsettling and disruptive ways.  The odd thing is that, for the first time in my MS life, I'm experiencing the denial phase that typically begins after a diagnosis.

It's been a wake-up call to come face-to-face with the harsh reality of MS, possible progression, and aging.

Life never follows a straight line.

When I first learned I had MS I hadn't a clue what was in store for me, the unexpected detours and undeniable disappointments that could lie ahead.

When you're young, and there's no internet to provide millions of reasons to worry about your future, you think you're invincible despite a medical condition.

What probably saved me from any mental hiccups was my fertile imagination, and the ability to jump into a daydream whenever I needed an escape.

Real-life problems were something that happened to others. I felt safe and healthy inside my self-created cocoon.

Ah, youth. 

I was fortunate to have two loves I could lean on for support.

One was an obsession with black and white films. Their Hollywood happy endings and bigger-than-life actors provided me with a haven. They'd transport me to places I never wanted to leave.

James Stewart, Cary Grant, and Katharine Hepburn in "The Philadelphia Story"

The second love was immersing myself in nature, spending hours and hours in the natural world of animals and plants.

Growing up in a home surrounded by woods I fell in love with the nighttime sound of crickets, watching the change of seasons, and the perfection of wildlife outside my door.

Nature taught me crucial lessons that still serve me well:

Classic films and the natural world are like old reliable friends who always have your back.

I wish I could bottle them as a panacea for the world's problems.

"If there's a single lesson that life teaches us, it's that wishing doesn't make it so."  ~Lev Grossman, The Magician

Life with MS

As I look back at my younger self, a wide-eyed twenty-something living with a disease, I realize how much I've changed.

Time has taught me the value of setting boundaries, ending toxic relationships, accepting truths, traveling through grief and pain, and struggling with the loneliness that comes with chronic illness.

It's a gut punch being unable to keep up with the rest of the world.

As a teenager, I felt a kinship with Henry David Thoreau after reading "Walden" about simple living in natural surroundings. He wrote his "life in the woods" while living in a cabin he built near Walden Pond in Massachusetts.

I'd kiss Thoreau on the cheek if I could thank him for all he's meant to me.

"Although truth can be found in literature, it can also be found in nature." ~ Henry David Thoreau

Living with MS has never been easy but as I passed my sixtieth birthday, and felt overwhelming personal and physical changes, I saw life through a clearer lens.

Like a butterfly emerging from a cocoon,  my metamorphosis was eye-opening and deeply challenging.

"Life is a succession of lessons which must be lived to be understood." ~Helen Keller

Life with MS

The BEAST of MS can be painful, unpredictable, and disturbing.

As hard as it is I still believe there's a silver lining to any situation if you look for it. What was mine?

The silver lining was realizing it was about time to start preparing for the inevitability of life's ups and downs. I decided to begin by:

Devoting myself to the list below is something that's within my control.

Now that's a silver lining!

(NOTE: I have no affiliation of any kind with the links below. I provide them for your enjoyment and hope you'll take the time to explore them for yourself) :

Inner Timer app
Cory Muscara 
Mindfulness.com app
Tapping
The Tapping Solution app
Chair yoga
Cornell Lab Bird Cam - Talk about a calming experience! Watch LIVE cams from around the world for "a virtual window into the natural world of birds." (We watch these on YouTube)

Here's when BEAUTY and the BEAST collide!

With so much going on in our lives my wonderful husband instinctively knew how to lift my spirits. After 34 years of marriage, we can read each other's hearts.

He took me on a trip to the New York Botanical Gardens and their gorgeous (a/k/a BEAUTYorchid show!

It was absolutely ah-may-zing. A completely magical day.

The BEAUTY was in the flowers, and the love, that I felt that day. I will never forget how special it made me feel.

Find something big, small, or anything in between that puts a smile on your face. Whatever it is it's what's right for YOU.

You. Deserve. Something. Special. Today. And. Always.

MS is only a part of who we are. Sprinkle the rest of your life with love and laughter.   

We are in this together. 

Now on with the show! Sit back and drink in these beauties that I posted just for you.


Life with MS

The Lessons We Learned From MS, COVID, and Each Other

Welcome back to An Empowered Spirit! I'm so happy you're here.

After taking a break from blogging for nine months I'm back and it feels wonderful being here with you.

The past two years have been so crazy that we all needed a break of one sort or another, don't you think? Sometimes it feels like we're living in a Robin Cook novel.

cat with big green eyes hiding under a blanket

Wake me when it's over!

One of the lessons we learned from the pandemic is how crucial it is to have a safe place to be nurtured and cared for when the world feels cold and out of control.

After I was diagnosed with MS many years ago, I searched for the best ways to cope with my new reality. It took a while, but I started finding answers to what I needed. When I created An Empowered Spirit, I wanted to share these insights with you on what helped me feel less lonely and afraid. The most important first step was finding the right...

Community.

There's magic and power in finding the right community, where people feel safe to tell their stories and share their feelings. The right community can offer unconditional support and comfort, and when you find that it feels damn good.

multiple sclerosis community

The power of community is the comfort and unconditional support you find with others

This year marks the tenth anniversary of An Empowered Spirit! A lot has changed in the MS landscape since 2011. What hasn't changed is my continued commitment to being a reliable source for you for all things MS!

To celebrate our anniversary we've updated An Empowered Spirit thanks to a generous grant from the HealtheVoices Impact Fund. I'm deeply grateful to HealtheVoices and Janssen for their continued support and generosity.

Multiple Sclerosis Blog Anniversary 2021

When I received the grant it was the nudge I needed. I'd been feeling burnt out from blogging, lost, and wondering what I should do next. HealtheVoices unknowingly pushed me into the "stop overthinking everything and just do it" mode.

So I'm getting off my tush to move in new and different directions for the next ten (+) years.

Like Michael Fox recently said about his journey with Parkinson's, it gets tiring to constantly make lemonade out of lemons. I quite agree. At this point in my life, I see a lot of things about life and MS differently, so I'll be focusing on topics with a fresh perspective. What will they be?

Wait and see!
MS
I'm busy planning new content to serve your needs, in creative. inspiring, and informative ways.

In return, I'd appreciate constructive suggestions or thoughts on what you're interested in hearing about. You can leave a comment below or reach out via the contact page.

What's new on An Empowered Spirit:

The new design of the blog reflects my love of every type of flower. They are beautiful and thrive despite adversity, just like the MS community.

Sixteen peony bushes are part of nature and this blog

My father planted sixteen peony bushes along our driveway. Here they are for your viewing pleasure.

“Like wildflowers, you must allow yourself to grow in all the places people thought you never would.” – E.V. 

Cathy Chester - MS Advocate - New Blog Header

CLICK on the HOME, ABOUT, MS RESOURCES, PRESS, and CONTACT buttons located at the top of the page to find exactly what you need.

"Out of suffering have emerged the strongest souls; the most massive characters are seared with scars." ~ Khalil Gibran

Disability and multiple sclerosis accessibility tool

NEW! An accessibility tool is located on the top left corner of every page to make pages more usable for you.

My mission continues to be to empower, inspire, and educate the multiple sclerosis and disability community, and their loved ones.

Now onto a special SURPRISE to start the celebration! Here's my first interview to christen the new blog. Drumroll, please...

After being interviewed twice by MS advocate, actor, voiceover artist, writer, and rapper Damian Washington I turned the tables on him. I chose Damian because he's smart, savvy, and very funny.

As Damian says, if you have to live with an incurable disease you may as well hang out with the cool kids.  He's definitely a cool kid.

Damian soared to the top of the advocacy game at warp speed and recently won TWO awards from WEGO Health: Hilarious Patient Leader and Best in Show: YouTube. Let me know what you think about our conversation.

 

With a party hat on and a grateful heart, thank you for helping us begin the next chapter of An Empowered Spirit in the best way possible: together. I've been enriched and inspired by your company and hope to see you return again and again.

END NOTE: Thanks again to HealtheVoices for your leadership program that supports the work of online health advocates. Your dedication and commitment to us are deeply appreciated.

 

Two Exciting Pieces of News for the MS Community

Being an advocate for the multiple sclerosis community means sharing information to help you stay aware of trending topics and credible information that can help you make informed decisions about your health. By sharing this information I hope to simplify and empower you on your MS journey.

multiple sclerosis awareness

Two organizations recently reached out to me about their new initiatives that I thought you'd like to know about.

 

NATIONAL MULTIPLE SCLEROSIS SOCIETY (nmss.org)

No one plans on being met with a life-changing diagnosis like MS – but whether you’re newly diagnosed or not, we can all use a little extra support. Our friends at the National MS Society put together a wonderful new resource called “Now What? Resources to Keep You Moving Forward with MS” and you can download it for free today.

multiple sclerosis awareness

From wellness to community to understanding symptoms, this guide is great for those with MS and those supporting loved ones with MS. As the NMSS website explains:

"Whether you were recently diagnosed or are processing a shift in your disease progression, you came to the right place. With you in mind, we created Now What? Resources to Keep You Moving Forward with MS. It's your introduction to the top resources and information from the National MS Society – news you can use to keep moving forward.

There's even more to discover on our website. This guide, however, offers the latest and most relevant information about MS.

Check it out by clicking HERE !

 

HEALTHLINE (healthline.com)

multiple sclerosis awareness

Photo: Courtesy of Healthline

There's a new CBD landing page and content hub we've built at Healthline. As cannabidiol (CBD) becomes a highly discussed product touting benefits across the board, especially for those suffering from chronic illnesses, we wanted to create an extensive resource for our audience to learn about what research has proven and what we still need more information on about CBD benefits. Specifically, research on how CBD can help autoimmune disease with articles covering topics such as how human studies have found that a combination of CBD and THC is effective in treating pain related to multiple sclerosis and arthritis.

CBD is helping to change lives, so we wanted to answer all our readers' questions. We hope you'll find the landing page a useful resource. Click HERE to find out more!

♦♦♦♦♦♦♦♦♦♦♦♦

Please let me know if you have any questions or comments. I always enjoy hearing from you. Have a lovely day!

NOTE: This post does not endorse or recommend any school of thought or product. This is for informational purposes only.

 

I Went Down a Rabbit Hole Trying to Figure Out Why My MS Drugs Cost So Much

I was recently introduced to Brian Howard, features editor of Philadelphia magazine, through a mutual friend. She said I must read his in-depth article about the exorbitant prices of MS drugs and how bureaucracy stands in the way of fair pricing. It delves into the same questions we ask: why are MS medications prohibitively priced, how are they negotiated, and how can we afford them?

I asked for Mr. Howard's permission to share his piece on An Empowered Spirit. I urge you to read on to learn about this important subject. I hope it will empower you to make informed decisions about the medications you use to manage your MS. 

 

Sky-high prices. Confusing co-pays. Maddening bureaucracy. Why is our pharmaceutical system such an impenetrable mess. 

By Brian Howard

Photo Credit: Ian Shiver

 

I was at the end of the long table in the conference room when I realized the drugs had become a problem.

As I tried to focus on the presentation — some suit droning on about tax benefits and pricing tiers — I zoned out, and my face became flushed. Burning-hot rage pulsed across my skin, crackled down to my fingertips, then shot back. I wasn’t sure I could make it out of the room without doing something I’d regret.

I’d always known that it could come to this — that the compounds I’d been injecting all these years could have consequences. Back then, even though I knew vaguely how much it all “cost,” someone else was always picking up the tab. And because I liked how the drugs made me feel — safe — I didn’t ask too many questions. You can’t put a price tag on security.

But suddenly, there was a price tag. And a big one. Specifically: 20 percent co-insurance after deductible.

This was going to get expensive.

I’m on drugs for multiple sclerosis and have been since 2004. MS meds are what are called maintenance drugs, meaning you take them daily or weekly from the moment of diagnosis till death or untenable side effects do you part. They’re also some of the most jaw-droppingly expensive drugs on the market. Today, in 2019, the four different name-brand medications I’ve been prescribed at different points in my treatment list for between $75,816 and $98,899. Per year. Prices are indeed high. And they’re going up fast.

Like everyone else, I’d been hearing the drumbeat: The cost of prescription drugs was out of control. But because the insurance plans I’ve been on had decent-enough prescription drug coverage — my meds had generally cost me a co-pay in the $100-to-$150-per-month range — I’d been shielded from the issue. And a few years back, I discovered that if you ask, some drug manufacturers will actually pay your co-pays for you. So I was getting drugs that listed for a decent annual salary for the cost of my modest-by-comparison health-insurance premiums. I didn’t know who was paying how much of those prices — honestly, they seemed too absurd to be real. All I knew was that it wasn’t me.

But as I sat in the conference room for my company’s annual benefits presentation last 

December, I got a cold dose of reality — and became another of the millions of Americans incensed by the skyrocketing prices pharmaceutical companies charge for their products and the byzantine, competition-squelching health-care system that allows those prices to escalate unchecked.

This year, Philly Mag’s parent company, Metro Corp, offered its employees, as it has each of the six years I’ve worked here, two plans through United Healthcare. What’s different this year is that due to the ballooning price of coverage, both Metro Corp plans came with prescription drug benefits that treat medications in the two highest tiers of its “formulary” (that’s insurer-speak for the list of drugs that are covered) on a co-insurance model, meaning I would have to pay “full price” for my medications until I hit my family deductible of $4,000 per year, and then 20 percent of the price afterward until I hit my individual out-of-pocket maximum of $6,650 per year. When all the math was done, it amounted to around $3,180 in additional, unexpected health-care costs over what I paid last year. It’s effectively a $3,180 pay cut — never good, and especially troubling heading into a year when you’re expecting your second daughter. My wife’s work provides good coverage for her but charges through the nose to add family.

I had to do some emergency rebudgeting. I’d need to find out what this drug was going to cost, fast. And, masochist that I am, I wanted to find out why it costs what it does.

What I learned: The pricing methods of drug companies in this country — largely unregulated by an innovation-obsessed, lobbyist-beset government and buttressed by taxpayer-funded research — are a big mystery. Thanks to secret negotiations, the prices that pharmaceutical companies list are different from the prices for your insurance company, which are different from the prices for your pharmacy. America’s health-care system is the most expensive and pointlessly complicated in the world — “a classic example of market failure,” according to Wendell Potter, the Philly-based former Cigna exec turned whistle-blower who’s now the muckraking publisher of Tarbell, an investigative journalism site focused on the health-care industrial complex.

As a result, it seems entirely possible that no two people in the country pay the same price for the same drug. And thanks to the bureaucracy that’s sprung up around health care like a boomtown, getting answers to even the most basic questions is increasingly difficult. Ultimately, what I’ve learned is that you might be able to find out how much a drug will cost you, but unless legislators take action, you’ll never know why.

To continue reading the article in full click this link for Philadelphia Magazine. 

 

Healthline Announces its List of Best MS Blogs of 2018

I'm thrilled that Healthline named An Empowered Spirit one of the best MS blogs of 2018. This is the seventh time my blog received this distinction and I'm as honored today as I was the first time.

Healthline

Thanks to Healthline for not only recognizing my work but also the work of other MS bloggers and organizations. They are helping us amplify our voices to reach a wider audience. I am deeply grateful.

Healthline

The world of MS has changed drastically since my 1986 diagnosis. It's hard to keep up with announcements about FDA-approved medications for MS and also those being tested with the hope of approval. There are also clinical trials, ongoing research, and important conferences, webinars, and podcasts to stay aware of. With so much information readers need to know who they can rely on to learn what they need to know.

We are fortunate to have so many MS organizations and bloggers who are dedicated to furnishing readers with the kind of information that will educate and enlighten them. No one needs to "go it alone" anymore.

I'm lucky to call many of these MS bloggers my friends - some I even spent time with at conferences or on panel discussions - and I'd like to introduce a few who share the honor of being named to Healthline's list. They are all exceptional people and I urge you to check their blogs. I guarantee you'll be glad you did.

While you're at it I hope you'll tool around An Empowered Spirit. Please come back often to read what's new in the world of MS. I promise to do my best to help you manage your journey in a more informed and (of course) empowered manner. Let me know what you think!

Here are some of my friends. Congratulations to all of them!

You can check out the entire list of Healthline's "Best Multiple Sclerosis Blogs of 2018" by clicking here

Join an MS Study from the Comfort of Home and Receive $50 for Your Time

Disclaimer: The following is sponsored content from DxTerity.

MS

 

Are you interested in helping advance research for MS but don’t know where to start? You’re not alone. Taking part in a research study for MS can seem overwhelming, but it doesn’t have to be.

A new at-home study called EMPOWER (Evaluating Multiple Sclerosis Patients ShOWing A GEnomic Signature of Therapy Response) is seeking volunteers with MS nationwide to better understand how MS affects the body. The goal of the study is to develop a blood test to help monitor disease activity and treatment response for people diagnosed with MS. The study is being conducted by DxTerity, a genomics company developing tests to better manage autoimmune diseases.

MS

Do I Qualify?

If you’re 18 years of age or older and have been diagnosed with MS (any type), you qualify.

Why Should I Take Part?

EMPOWER is an at-home study that can be completed in your free time. All you need to do is sign up online and a study kit will be mailed to your home.

What’s Next?

Follow the instructions in the fingerstick blood collection kit to collect a few drops of your blood (much like at-home glucose monitoring). Mail your sample to the research lab using the prepaid envelope.

When you’re done, log in to the secure study portal and complete a short survey online. You will be compensated $50 for your complete study participation, which you can keep or tell DxTerity to donate to an MS charity of your choice. That’s it!

MS

Ready to make a difference in MS research? I know I am. Click here to get started.

NOTE: All questions about DxTerity's EMPOWER study and the test should be directed to DxTerity. Click here for contact information.

How My First Video "What I Wish I Knew" Will Inspire You

A few months ago my husband, son and I were asked to be part of a video series on living, and supporting those living, with MS. The theme of the initiative was:

I have MS. I have a team. I have a future. 

Here's the trailer:

https://www.youtube.com/watch?v=lfY209PUr-c

I was thrilled about this important endeavor and the three of us jumped at the chance to be part of it.

I relished the notion of using my voice on camera, something completely different than expressing my thoughts through the written word.

I sat down and wrote my script, polishing it until I felt my message was both interesting and informative. I watched my favorite TED talks for pointers on how to look on camera. I purchased a new outfit that would be comfortable and chic. And I held my breath the morning of the shoot as the makeup artist applied her palette of colors to my face.

I was told my segment should focus on the idea of "What I Wish I Knew."

What did I wish the younger ME knew after being diagnosed? What didn't I know then that I know now? What lessons did I learn along the way? What pearly words of wisdom could I pass on to help others manage their journey better than I did?

I hope you'll find time to sit back, listen to my story and tell me what you think. Go easy on me! This is my first time alone on camera....

My next blog post will be another video called "It Takes a Team" with my husband, son and me. We didn't write a script. We simply sat on a couch and spoke directly from our hearts.

You can view other videos in the MS TEAMWORKS series on the Catamount Medical Education website. Subjects include: The Roadmap to Motherhood, Integrative Medicine, I'm Getting Worse - What Does That Mean, I Wish My Healthcare Professional Knew, How I Manage My MS, and many more.

My thanks to the people at the Consortium of Multiple Sclerosis Centers, Catamount Medical Education and support from EMD Serono for this wonderful experience.

How Words Like "Cure" Can Exploit A Community

The misleading headline Meet the Cambridge Scientist on Verge of Curing Multiple Sclerosis caused some hysteria in the MS community this week. I was sent several private messages, texts and emails from people who love and care about my welfare. Their thoughtfulness touched my heart.

The story was about a Cambridge scientist who sees a solution to the disease using nanotechnology which has garnered some interest from two large pharmaceutical companies and the hope that investors will help fund the “ambitious” target date of 2020 to begin clinical trials. (If you are interested click here to see their pre-clinical trial results.)

How words like cure can exploit the MS community

"Cure" for MS is just click bait

A cure for multiple sclerosis from this therapy is not around the corner, if at all, yet the media decided to exploit the MS community with their headlines. This caused quite a stir for hopeful patients crossing their fingers.

Shame on the media for putting aside journalistic integrity in favor of higher viewership.

In the era of fake news and alternative facts we must be careful with our words. They matter. Headlines and books written at the expense of other’s misfortune are cruel and offensive.

It makes me crazy to read some of the empty promises lining the sponsored ads of my Facebook newsfeed. I’ve cured myself! I’m symptom free! You can beat this!  

Nope.

To get a therapy approved researchers must test them in laboratories. The most promising ones move onto clinical trials to learn more about treatment, risks and effectiveness. There are then three phases to clinical trials and in Phase 4, after the therapy is approved and made available to the public, the therapy continues to be tracked for safety, risks, benefits and optimal use. The amount of time it takes to complete a clinical trial varies. It can take from 10 - 15 years to complete the first three phases even before the therapy is licensed.

Alternative medicine and MS

Over the years I’ve been told to try bee venom, remove amalgam fillings in my mouth, use magnet therapy, go on a low-fat (and high-fat) diet, have my spine manipulated, use a large amount of supplements including minerals and coral calcium and drink aloe juice to ease the symptoms or cure myself from MS. I’ve done none of these.

Some CAM (complementary and alternative medicine) are regulated by the FDA but many are not.

Be wary. Do your research. Ask questions. Reach out to others. Talk to your doctor.

I reached out to fellow advocates who I now call friends to discuss this latest claim. I knew what I thought but wanted to hear their opinions. They didn’t disappoint.

This blog post is one girl’s opinion about the state of cures, scams and journalistic pride and integrity. If you agree or disagree I’d love to hear your constructive opinions. After all, it takes a village.

Here’s to your good health.

Skip to content