My Brother, Anand

As the video pans out, pain sears through my body as I watch him “walk.” Feeling somewhat queasy, I cannot take my eyes off from this young man living in Kolhapur, India as he carefully crosses the colorful and well-kept room with his thin CMT legs and horribly twisted feet. Each cautiously placed step reveals the soles of his feet, which are perfectly perpendicular to the opposing ankle. I’ve seen bad cases of supination, but it looked like his feet just decided to fold to the inside, forcing the tips of his tibia and fibula to bear his weight.

His hands are also terribly affected by CMT. A close-up reveals clawed fingers, stubbornly bent, refusing to move. Managing a few callisthenic-like arm movements, it becomes apparent that CMT has also ravaged his hands, leaving them weak and atrophied.

 

His email, video attached, found itself in my inbox.

Jan 30, 2013

Dear sir/madam

As you know I have CMT & I am from India. There is no awareness about CMT compared to your country. So please give me information on what type of care should I take. What type of exercise should I do? What type of shoes should I  wear?
Please help me. I am forwarding my video clip.

Anand Pramod Patki

 

I immediately emailed him. From that day, 4 years ago, Anand has become a close friend….my brother.

His story goes something like this: Anand started showing signs of CMT at 6 years old. His toes started to claw and the muscles in his lower legs were weakening.

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Anand – Age 6

 

By the age of 10, he was unable to stand upright in one position for more than 2-3 seconds without losing his balance.

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Anand – Age 10

He was 15 years old at his sister’s engagement party, but he could no longer walk long distances as his feet started to curve inward.

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Anand – Age 15

 

Despite the challenges of living in India with a physical disability, Anand finished high school and even received the 2nd highest grade on his high school board exams. A writing aid was offered, but Anand refused, insisting on independently write the answers to a grueling 3-hour long exam.

Officially diagnosed with CMT at age 20, his neurologist outright told him: “There is no treatment and you will become weaker and weaker.” With limited resources, information or support, Anand found the strength to mentally accept the diagnosis, and to retain a positive outlook on life.  He had a supportive family, parents, intelligence and deep inner fortitude.

When he reached out to the CMTA, he had been working as a computer operator at the Postal Department in India. There is no Americans with Disabilities Act (ADA) in India. To keep his job, and to make up for his slower than average data entry work, he had to work continuously for more than 8 hours at a time, without the luxury of a single break. Even the bathroom was off limits. Even if he had had the time, handicapped bathrooms are few and far between in India.

Yet, Anand emphasized, “I am enjoying my job. At this stage, I cannot walk without support on hard surfaces. I face a lot of problems performing my day- to- day tasks, like buttoning my shirts, wearing my shoes, counting cash, handling vouchers, inserting paper in the printer, etc.  I’ve also had a chronic ankle injury for the past five years. But, I am happy in my life. I have no complaints with my God.”

I communicate frequently through email and Skype with my Indian friend. Each correspondence brings us closer. I marvel at his optimism, boyish grin and resolve to live the best life possible despite all the obstacles he faces every single day.

But what could I do? Except for Anand and his family, I know no one in India. His town of Kolhapur is a mere 8,500 miles away from where I live in California.

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Yet, as we wrote back and forth, the possibility of foot surgery was discussed. Even if we did stumble upon an orthopedic doctor, would he be able to correct Ananda’s feet?

After months and months of searching, I turned to Dr. Glenn Pfeffer, who put me in contact with Dr. Rana, a well-known orthopedic surgeon who practices in New Dehli and was willing to take on this complex procedure.

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Dr. Rana

 

With the precious support of my colleagues on the CMTA’s Board of Directors, Anand was given the opportunity to have a potentially life-changing surgery.

2 years after meeting Anand, surgery was scheduled for April 18, 2015. Dr. Rana would perform a triple arthrodesis (fusing the three joints in the hindfoot) with Achilles tendon lengthening on each foot, one week apart. To get to New Delhi, Anand took his first-ever plane ride with his Baba (father), after which he enthusiastically wrote: “I was feeling like a free bird who flies in the sky!”

The surgeries went well, but there have been some complications due to low bone density, pressure sores, and screws not wanting to stay in place. Anand has waited patiently while healing and has had to undergo several smaller procedures to remove those uncollaborative pieces of metal.

With the help of thick plastic leg boots, today, Anand is able to walk on the soles of his feet.

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Watch this:

 

 

When he went back to work, his colleagues were thrilled to see him and stood, applauding his return. In 2-3 months, the braces will be exchanged for lighter, more user-friendly AFOs. The day that he is able to put on a pair of shoes, will be the day that we celebrate and consider the surgery to have been 100% successful.

Skype has been a wonderful tool. Virtually I have visited Anand in India and he has spent time with us in California. Yet, virtual reality will never be on par with being able to physically hug my brother, sit next to him, enjoy a meal, laugh, cry, talk. My dream is to visit him in Kolhapur. And I will and look forward to the day we can walk, arm in arm, down the street with my brother.

 

Anand’s Words of Wisdom

As you can see, I am getting weaker and weaker physically, but becoming stronger and stronger mentally. I cannot tell you that you will be victorious over your CMT, but you can manage the degeneration process of CMT by following these steps:

  • Always think positively.  To train your mind to think always positively is essential.  I believe in God and I also believe there are positive waves in nature.  So, you can change your life with positive thinking.
  • Remain hopeful. Don’t feel sad in your life. Our scientists and researchers are doing a lot of experiments on CMT. I know in next five years, we will get very close to making a world without CMT.
  • Don’t think of yourself as disabled. You are ‘specially- abled ‘. I know we cannot do much about our physical capacity, but you have a normal brain. Use it with your full capacity. Be honest and work hard in your job or field and try to become specially- abled .
  • Thank God. Don’t curse your God because God has gifted you with a super brain. Use it as your sixth sense. God has gifted you with normal eyes. Use them to see beautiful and good things in your life. Be satisfied and happy with what you have. Do not feel  badly about what you don’t have.
  • The most important thing is to maintain your physical capacity and try to improve it with proper exercise. For me, Yoga is the best option to improve my muscle flexibility.

Isn’t he somethng?

 

My Name is Not Grace

Dedicated to all my friends who have a love/hate relationship with shoes.

“I love those shoes….OMG – they are sooooo cute!” enthusiastically commented an unknown, young, attractive, athletically built woman.  I looked around, certain that she was addressing someone behind me or outside my range of vision.  Mouth hanging open, I stood stunned, realizing she was referring to my shoes, my size 12 purple and aqua blue Solomon running shoes. Managing to spit out a “Thanks!” her casual compliment rendered me speechless for all of about 5 minutes (which seemed like an eternity…..to me).

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Above: The Complimented Shoes 

 

The last time someone actually told me they liked my shoes was back in September of 1967. I was 5 and my mom had just bought me a pair of black, shiny patent leather shoes. The compliments I received! Overjoyed with my new shoes I ran, jumped, danced and then, never fail, I slipped on our hardwood floors, landing head first into the electric radiator, at the base of the wall. As blood gushed from the gash on my forehead, a cloth was applied to the wound where it stayed until we reached the ER. The stitches left a small scar above my left eyebrow, a foreboding symbol of future foot-related misery.

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Above: Me, Age 5, Patent Leather Shoes

Nevertheless, I had not yet received the memo about imminent foot woes, so when my mom had to order new and very expensive shoes and winter boots from a shop in Montreal because my instep was so high, I thought that I was really something special.  Although I hadn’t a clue as to what a high instep actually was, I didn’t care. I felt like a princess who needed the best of what money could buy, and from abroad, to boot (a 2-hour drive from my hometown of Burlington, VT).  “I could get used to a life of royalty-Queen Elizabeth,” I imagined, my illusions of grandeur already a problem at such a young age. The thrill of ordering our butler around, “Andrew, Caviar, please! “or “I’ll wear the dazzling rubies this evening, Alfred! Snap, snap…I haven’t got all day!”

As I grew taller, my feet inevitably grew longer. By 8th grade, I was at least 5’7’ and my feet already demanded a size 10 shoe. Long-limbed and gawky, I looked like a baby flamingo and walked like a newborn giraffe learning to take its first steps. Between the giraffe and the flamingo, I must have looked a lot like a fliraffe.

 

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Above: Baby Flamingo

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Above: Baby Giraffe

 

 

 

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Above: Fliraffe (a giraffe with baby flamingo feet)

 

If my parents had named me Grace, I would have been a laughing stock! It was bad enough with older brothers who had their own nicknames for me: clumsy, klutz, horse, big foot, clod, butterfingers, spazz, etc. I was always bumping into something and spent a  lot of time on the ground, either cleaning up something I had spilled or nursing wounded knees.

If you have CMT, you may be able to relate to my story and have a few of your own. Does this sound familiar? I fall over air, get caught up in my own feet, trip up stairs, run into furniture and constantly drop things. Here are just a few concrete examples which come to mind: I dropped my cell in public toilets, twice, got my bike tire caught in the rails of a tram, and just simply fell over onto my side in the middle of a busy plaza, tripped on nothing and everything, sprained ankles, broken toes and sported many, many bruises. And this is just the tip of the iceberg, as the list is way too long and the catastrophes, too many to count.

Many of my friends in high school and college wore high heeled shoes for events. Not me. At 5’9’’ I was already taller than the majority of other students, especially the guys. Secondly, a size 10 high heeled shoe was impossible to find and third, I would have broken my neck.  And have you ever found a sample size 6 or 7 shoe at the store, and when they brought out the size 10 or 11, it looked nothing at all like the size 7 you had already fallen in love with?

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Above: The shoes I wanted (floor model,size 7)

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Above: The shoes they brought out (size 12)

When I lived in France, the saleswoman wore a look of shock and disgust when I gave her my shoe size. As if being forced to wait on the Hunchback of Notre Dame, she nervously whimpered, “Madame, s’il vous plaît, look in zee secshun for zee man,” and she pointed in the direction of the men’s shoe department. How humiliating.

By adding padded and ultra cushy orthotics, my shoe size increased by 1 or 2 sizes!! On my body, an 11 or 12 shoe is not feminine. It just isn’t. I walk more like Herman Munster than a tall woman with long legs and big feet.

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Above: My body and feet

So when my new best friend complimented me on my “cute” shoes, I decided to take the compliment and wear it with pride. And, honestly, I am just grateful to be able to walk. Some are not so lucky. So, I say screw femininity.  The older I get, the less I care about what people think, especially if it is negative. Now give me positive commentary, and that my friends, is a different ball of wax.

Crotches and Belt Buckles: Cocktail Party Blues

The pizza had just arrived.  Before I could take my first bite, the subject of my husband’s company cocktail party surfaces. “Thanks, but no thanks. I don’t want to go,” I say with steadfast determination.  “I’ve already made sure that chairs will be available,” he counters, attempting to make the event seem easy, cozy, attractive even. Then, as he points at me with the tip of his piping hot slice of pepperoni pizza, he gets all serious and a little pouty.  “Look, I  run the company. It would mean a lot to me if you came.  My staff and colleagues are looking forward to meeting you. ”  On the inside, I roll my eyes, feeling a little irritated that some of the melted cheese from the pizza was still stuck to his face. If I’m not there, who will make sure he wipes off his chin, which was now dripping with grease and mozzarella?

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Resigned, and feeling slightly manipulated, I agree to join in on the merriment.

Gilles’ mom once told me that sometimes you just have to do things you don’t want to do, like get a root canal,  euthanize your pet lizard or unplug the toilet.  And, going to this cocktail party was right up there in the category of things to avoid.

At cocktail parties, everyone usually stands around with a drink in hand, eating hors-d’oeuvres and chatting. I’m all good with the chatting and eating part. I also enjoy meeting new people. It’s the standing around that is the most difficult. When it hurts to stand for more than 5 minutes because of nerve pain in your feet, it is hard to feel relaxed at these events.

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After no more than 5 minutes after our grand entrance,  my anxiety rises and I desperately scan the room for a chair or something to lean on. Rocking back and forth, relieving pressure first on the right foot, then on the left,  the right, the left, I wondering if the other guests are noticing my discomfort.  So as to not look too silly, I  even start bopping my head and swinging my hips to the beat of the music, as if I were lightly dancing and really into the melody. (This probably made me stand out that much more, but at the time, it seemed reasonable.)

10 minutes is my max tolerance before  I excuse myself from whatever superficial conversation I am engaged in and plop down right into the arms of my new best friend- the chair. Thank God – the pressure is off of my aching soles. I wave to Gilles, just to show him where I’ve landed. Colleagues in tow, Gilles slowly makes his way toward me and over the noise, the music, the laughter, I overhear, “…… foot problems……can’t stand too long…..pain.”  One of his cohorts, wearing a glittery cocktail dress and 10-inch heels chimes in, trying to relate to my situation, “Oh, my feet are killing me too! Ouch! I just have to slip these off….what women wouldn’t do to look their best! Staring down at my bulky size 10 (mens) hiking shoes, I could not take it anymore. “OMG, can we leave now?” I pleaded to deaf ears. “I just can’t relate to these people and they obviously can’t relate to me.” But, my protests were drowned by the noises of background laughter, glasses clinking and live, blasting music.

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Loving the comfort of my chair, people politely stop by to say hi, but no one really wants to sit with me. Why? Because it is a COCKTAIL PARTY and people STAND at cocktail parties. As a seated attendee, engaging in casual or meaningful conversation with a standing guest just translates into craning of the neck in an upward position for an extended amount of time. The result? A trip to the chiropractor’s the following day. So, to bypass unnecessary appointments and self -afflicted neck pain, I set my gaze forward, looking straight in front of me. From this vantage point, the scenery is mostly just crotches and belt buckles.  That’s exactly what I wrote – crotches and belt buckles!! Yep. Can you say, awkward? What’s worse, if the room is crowded, intimacy is quickly forgotten with up-close views of back pockets and butts. Feeling pretty helpless, I just end up praying that no one passes gas too close to my face. Escape would be difficult.

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I usually get a few stragglers who spend some time talking about how mean Gilles is as a boss (just kidding), but mostly I pretend to be really busy on my phone, answering urgent messages, texting and making note of some vital, earth-shattering information.

I’m usually overjoyed when it is time to leave. Another holiday party over. Check! In all honesty, I think I would have rather unplugged the toilet.

There is no moral to this story, but here are a few thoughts:

  1. If you want to see crotches and belt buckles up close and personal, attend a cocktail party. Make sure to sit for the entire duration of the party so you’ll be able to relate to my experiences.
  2.  Feign sickness and just don’t go to standing only events. Stay home, watch a movie and cuddle with your cat or dog. It’s much more relaxing and the therapeutic value is undeniable.

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