An Empowered Spirit Blog Post

Ann Romney: How Horses, Determination And Courage Can Create A Joyful Life (Book Giveaway)

By Cathy Chester on October 14, 2015

joyful

Once upon a time there was a little girl who lived a perfect life. Her hopes and dreams were like any other little girl and with each passing year her blessings grew exponentially. Her future looked perfect and bright.

Never in her wildest dreams did she imagine that one day she’d grow up and receive a diagnosis that would change her life forever.

Does this story sound like someone you know? It could be the story of countless women whose lives change abruptly, from skipping down the yellow brick road to being suddenly stopped in their tracks.

But this particular story belongs to Ann Romney. Yes, that Ann Romney. The one married to former Governor of Massachusetts Mitt Romney and the daughter of Edward Davies, former Mayor of Bloomfield Hills, Michigan and a self-made industrialist.

joyful

Photo: macmillan.com

In her heartfelt memoir “In This Together” Mrs. Romney chronicles her journey of living with Multiple Sclerosis from her diagnosis in 1998 to today.

“Mitt and I had gone home from the hospital the day I was diagnosed with a brochure about MS that answered all of our immediate questions; it felt like we’d bought a washing machine and were given a pamphlet outlining the extended warranty.”

Hearing about Ann Romney’s MS - from the shock of diagnosis through acceptance, to finding what medications and modalities worked for her - felt a lot like reliving my own story.

But let’s be honest. We all know that Mrs. Romney’s wealth and notoriety would provide her with the gold standard of healthcare that many in the MS community (and many others) can ill afford. While that may be true, we also know that MS does not discriminate. Her struggles with the disease are the same as ours.

With the support of her family, friends and medical team Mrs. Romney faces her illness head-on, with an open mind and never-ending curiosity to learn all she can.

“As I began adjusting to my new reality my physical condition got worse every single day. It felt like there was a wildfire raging through my body. I would wake up in the morning wondering what part of my body would be attacked that day. The numbness in my leg had started at a spot near my knee; it had now travelled all the way down to my toes and up my torso.”

Ann Romney is unlike me in many ways. I have one son; she has five. I am a Jew; she is Mormon. I am a liberal; she is Republican.

Yet as I read her story I saw more similarities than differences between us, and in those similarities I cultivated a sort of bond with Ann (yes, I now feel comfortable calling her by her first name!)

During a recent call-in provided by St. Martin’s Press I had an opportunity, along with other MS bloggers, to ask Mrs. Romney some questions. The first thing I learned and was thrilled about was this: All proceeds of “In This Together” will go to Brigham & Women’s Hospital Center and to neurologic research:

“I’ve been thinking about it a lot and talking to some other colleagues and honestly, what I do helps with Parkinson’s and other illnesses. He said, they’re more related, we’re finding, than what we thought. It was his idea to broaden it to MS, Alzheimer’s, ALS, Parkinson’s, and they also found that some of the drugs they were using for MS, was helping with the treatment of a previously inoperable and incurable brain tumor. So, they included brain tumors as well. So it’s going to be unique. We are going to have all of these researchers and scientists under one roof. There will be obviously the research going on, there will be diagnostic testing, there will be treatment, and doctors’ visits all under one roof. The center will open next October, right across the street from Brigham and Women’s Hospital.” ~Ann Romney, on her discussions with her neurologist Dr. Howard Weiner on the opening of the Ann Romney Center for Neurologic Diseases

Ann was diagnosed at a time where there were approved MS medications, and while there were none when I was diagnosed we were both told by neurologists to go home and wait for our next flare-up.

We both were wise to ignore their advice.

Ann began a journey of exploration to find ways to continue living the full life she was accustomed to living while attending to her wellness needs at the same time. Her lifelong love of horses proved to be one of her keys toward wellness. A childhood passion, horseback riding helped Ann cope with the emotional baggage of MS.

“Taking up riding had made a fundamental difference in my life. Instead of wishing that I would die quickly rather than being devoured piece-by-piece, as I had been thinking only a few months earlier, it helped me learn how to live with my disease.”

She also remained open to alternative paths for her wellness. She explored reflexology and cranial sacral therapy, finding therapists through recommendations. It was fascinating to read the details of these experiences, prompting me to begin my own search into them.

I recommend Ann Romney’s book to anyone living with MS, particularly to those who are newly diagnosed. She writes her truth with courage, a positive attitude and what people used to call "moxie." It’s not the Pollyanna story you'd expect from someone famous. There's no spoiled little girl here. In fact it’s quite the opposite. Ann Romney illustrates her worst fears along with her best, showcasing the struggles we all face, with all illnesses, alongside of her own. She is the perfect role model.

a Rafflecopter giveaway

DISCLOSURE: I received a free copy of “In This Together” from St. Martin’s Press. All opinions expressed are, as always, completely my own.

I am happy to provide three free copies of “In This Together” to three lucky winners. Leave a comment and follow instructions provided by Rafflecopter. Contest ends October 22. Winners will be notified by email. Good luck!

NOTE: I thank Mrs. Romney and Dr. Howard Weiner for creating a center geared toward research for not only MS but also Alzheimer's, ALS , Parkinson's and brain tumors. I hope you'll check it out:

The Ann Romney Center for Neurologic Diseases will be at Brigham and Women’s Hospital in Boston, Massachusetts (BWH) is a collaborative global pursuit to accelerate treatments, prevention, and cures for five of the world’s most complex neurologic diseases: multiple sclerosis (MS), Alzheimer’s disease, ALS (Lou Gehrig’s disease), Parkinson’s disease, and brain tumors.

 

 

 

 

 

 

Author

Cathy Chester

Comments

  1. Sounds like a fascinating book Cathy! We may come from different stations in life, but when it comes to these horrible diseases it just doesn't matter what is in your bank account.

  2. I read everything I can get my hands on about MS. You never know what you might learn. Would love another book to add to my collection. X

  3. This is a lovely review Cathy. I am looking foward to reading the book.
    Disease certainly doesn't discriminate and no matter where we are on economic scales if there isn't a cure there isn't a cure.
    Brigham and Women's is an amazing hospital. I believe they are capable of finding cures for all of these diseases.

  4. Thanks so much for sharing. I love Ann Romney and her openness. The MonSter is unaffected by money. Research and Coordination of information is needed. Thanks, Ann Romney! Mary Gerdt mononucleosis age 19, nurse age 22, rrms diagnosed age 49, disability 56, closet republican, blogger, tax victim.

  5. There is a constant message, it seems, and that is "don't believe the dire stuff" and "take charge of your own treatment, recovery, illness." I find these the most inspirational posts of all, they teach us so much. Thank you, Cathy.

  6. I love reviews where the reader is affected personally - and you've nailed this one, my friend. I look forward to reading this book someday. Whether I win a copy or not.

    I shared on FB, too. 🙂 Great read.

  7. An inspiring person (like you!) whose story of courage and being proactive will help so many people. I think this applies to life in general - learning how to push forward, make the most of what you have, and work hard to overcome all obstacles. Of course, we don't always have the power to do that, and that's why it's so important to learn from others.

  8. Lovely sharing, Cathy. Truly. We can never know too much about this disease. Like any other, it does not discriminate. I can't imagine. Blessings!

  9. Attitude impacts everything, but that said, disease is NOT due to having a bad attitude. My husband researches in this area, neurochemistry, peptides, and such, and we need more research funding for pure research. Most research that happens at med centers has gone on for years, or decades, before moving up the pipeline to trials. We need to use our knowledge and not just what can make a pharma company more bucks. Great piece, Cathy!

  10. I received my MS diagnosis in the spring of 2012. Watching an active, energetic Mrs. Romney on the news everyday encouraged me tremendously! If asked a question about MS in an interview, she was always honest and never overly positive. All of these observations made a big impact on me as I wrestled with my new normal.

  11. While I would never wish a disease on anyone, a high profile person can bring visibility that results in more funding, donations, research, etc. I applaud Mrs. Romney for speaking out. Thanks for sharing your thoughts about her book and I wish her much success.

  12. Hi Cathy,

    I'm so happy to hear the proceeds are going to research.
    Just from the snippets I read I'm interested in reading the entire book....
    I'm facing a huge fear...a divorce about to become final. It was a 4 year marriage. I was diagnosed one month after we married. My illness has definitely played a role...friends have helped with tasks but it's wearing thin....I will be moving to a trailer park from a home I have owned on my own since 2002....I'm terrified but I've always been a strong woman and I will get by somehow...
    I will be living on only my disability income and that's my biggest fear...I had a successful career and it ended just before diagnosis...I really feel that's why my husband left me. He worships money. I know I'm better off spiritually but I will be poor for the first time since early childhood....maybe someone would publish my book...?

  13. Thank you Cathy for such an inspirational post about Ann. It will be great to certainly get this book to read as its true, people living with the same medical condition share the same issues in life irrespective of grrowing up differently or having a different liking / support or belief. Many thanks once again for posting. Best Abhs

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