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One of the hardest things I’ve ever been told is that I would be living with avascular necrosis the rest of my life. Worst, that I’d be in a wheel chair. It’s been 19 years since my AVN diagnosis and if I could go back to that day, this is is what I would tell myself.

One of the hardest things I was ever told was I would be living with avascular necrosis the rest of my life. Worst, told you will be in a wheel chair at the age of 21. Living with avascular necrosis or any chronic pain comes with challenges particularly with exercise and dieting.

I was a senior in college going out with friends one night when suddenly, something gave in my leg.

I was lying in the middle of a busy road and couldn’t walk.

A friend pulled me off the road. While someone called 911, he called my parents. He was shaking the whole time, and held me until the ambulance came. I think he was more scared than I was.

My parents arrived the same time the ambulance did and I was rushed to the hospital where they determined my femur broke. I’d been having a strange pain in my leg for weeks and had an x-ray done at urgent care days before the accident but nothing showed.

parasailing

Months earlier I was parasailing in Spain.

I was told the fracture was severe and required surgery. They didn’t do surgery until the next morning though.

I’ll never understand why surgery was didn’t happen until 8+ hours later. Every minute of blood loss to bone is critical. Ultimately this mistake is what lead to my AVN diagnosis .

Looking back, I know without a doubt my hormone problems manifested in this fracture.

The femur is the largest bone in the body and hardest to break. This should have been a red flag to doctors that something was wrong with my body.

selfie-gym

When I woke from surgery, I woke up to my worst nightmare.

I had a huge scar of staples from my hip that extended to my knee. I immediately thought what man is going to want me now? I’m botched. I’m not a woman. For days, I didn’t talk. It was just too horrifying to be real life.

When they made me move, I wanted to die. The pain was unbearable.

I was on crutches 3 months. Couldn’t drive, couldn’t shower, couldn’t walk to class. Did I mention it was my senior year of college in Wisconsin in the middle of winter? Thankfully I had amazing roommates, friends and parents who helped. Without their help, I wouldn’t have graduated that year.

scar

My scar today.

Once I was released from crutches, I had to learn how to walk again.I lost all muscle in my right leg and was extremely weak.

The orthopedic never suggested physical therapy.

I will never understand that given the severity of my injury. But I was a fitness instructor and worked out frequently before the accident so I started going to the gym and gradually regained strength.

A year later, the pins removed.

It was the greatest relief. Those pins hurt with every step I took. I swore they were near a nerve because that pain was intense and never went away until they were removed. Six months after the pins were removed, I couldn’t abduct my right leg. It was locked.

I was 22 when I was diagnosed with avascular necrosis.

avascular necrosis

The prognosis wasn’t good. My right femur head had died from lack of blood supply and would only continue to deteriorate. I was referred to Mayo Clinic. When I got there, I was optimistic they would do something, but left with the most horrific thing a doctor has ever told me.

I was told by two doctors in not so sensitive terms, I needed a hip replacement in 6 months and needed to prepare myself for a life in a wheel chair. What’s worse, I was told NOT TO BE ACTIVE.

The doctors insisted I stay off my feet to protect what little bone I had left.

I was devastated.

For 10 years, I did what they said. I did nothing. I sat around, placed limits on what I could or could not do, passed experiences and missed living the best years of my life. They’re doctors. They know everything. Or at least that’s what I thought.

Until one day, I had enough and started walking.

Walking

If there were ever a moment in my life I could point to as my turning point, it was the day I started walking. I no longer told myself I couldn’t anymore. From that moment on, I told myself “I can.”

I can lose weight. I can be active. I can live life. It was the best healing I ever did for my body.

My AVN pain literally disappeared as the weight did. Today I’m in 90% less pain than I ever was overweight. My high level of activity also keeps the joint mobile which equates to less pain.

Today I wish I could go back to those doctors, shake my fists at them and tell them how wrong they were, how ashamed they should be for giving so little hope to someone.

1238806_10202155834760678_1923270940_n

A positive approach is more advantageous to a patient than a negative one.

Over the years, I’ve interviewed several doctors for my hip surgery knowing it was something I would be faced with eventually. Every doctor I’ve seen has been amazed how I’ve gone 18 years without surgery, stating scientifically it’s impossible. My response?

“It’s not impossible, it’s because I’m active.”

I knew I found the right doctor when I found one who agreed with me. He said he wished every patient understood the value of activity to pain management. Unfortunately, not every patient has my outlook because not every patient is willing to fight for their health the way I did. Many people accept what the unhopeful doctor says.

You never wake up one day expecting your life to be turned upside down by illness.

swimming

It just happens. And you do the best you can to deal with it in the best way you can, which may not always be what a doctor tells you. I’m not saying doctors are wrong, but I am saying you can do anything you set your mind to. If I had to go back, I would tell myself to…

Have faith. Never to lose hope. It will be hard, but your mind will take you where you want to go and your body will follow.

I have several tips for dealing with avascular necrosis and the type of workouts that helped me. As for diet, I focused on losing weight by watching my calories, portion sizes and eating more nutrient dense foods. There is no cure for AVN, but certainly losing weight made the pain more tolerable.

In September 2016, I had a hip replacement effectively removing my AVN. You can read about my hip replacement in these posts:

Too Young For A Hip Replacement

What To Expect Recovering From A Hip Replacement

Disclaimer – the advice in this post is general advice. It’s not intended to treat or diagnose. As a health care professional, I cannot give individual medical advice unless you are a patient of mine. This is for legal reasons and to protect your health. I am NOT an orthopedic doctor. DO NOT send me your x-rays or medical information. Please consult with your orthopedic.

If you are a woman over 35 with 20 to 50 or more pounds to lose and ready to lose weight and feel great, watch this free weight loss training to get started.

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Megan

Megan is a nutritionist who coaches women 35+ lose weight sustainably. She is the author of the Low Calorie Cookbook, fitness instructor, host of the Dish On Ditching Diets Podcast and creator of Skinny Fitalicious where you get lighter, higher protein recipes. Follow Megan on Facebook, Pinterest, YouTube and Instagram for the latest updates.

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70 Comments

  1. Courtney Bentley says:

    What an incredible story! Let me tell you, I am a total believer of listening to YOURself! I totally had doctors telling me I could NEVER get pregnant, my body was completely out of balance when really I knew all I needed was to eat more carbs. The minute I ate more complex carbs my hormones leveled to normal and I get my period every month around the same time, I am completely normal its funny because these doctors had me on all kinds of medicine and didn’t believe that nutrition was the big factor! Thanks for sharing your story!!

    1. Megan says:

      Wow! That is incredible you were able to do that. I am a firm believer that science is not the end all be all. Thanks for sharing!

  2. Blair says:

    Cheers to you, my friend. You are a tough lady!

    1. Megan says:

      Thanks Blair!

  3. Casey the College Celiac says:

    Thank you so much for sharing your story! As someone living with two chronic illnesses (fibromyalgia, an autoimmune condition that causes widespread pain and celiac disease, another autoimmune condition in which ingesting gluten causes intestinal inflammation), I know that being active while you’re in pain is definitely not easy. I fully believe that being active has helped lower my pain from fibro, though and learning to love healthy eating and homemade meals has made adjusting to a gluten free diet much easier. When we lose so much control over our bodies thanks to chronic diseases, it’s so important we do what we can to fight back!

    1. Megan says:

      I am gluten intolerant and also have Hashimoto’s so I can understand where you’re coming from. I love that you haven’t succumbed to it. I was hoping when I wrote this to let others know that they are so much more than a disease or chronic illness.

  4. Jody - Fit at 58 says:

    SUCH INSPIRATION!!!!!! Thank you for sharing!!!

    1. Megan says:

      Thank you friend <3

  5. Erin @ Erin's Inside Job says:

    AH I LOVE THIS. I can imagine the cynicism you prob have towards the medical community and I’m glad you took some responsibility for your own health and challenged the limits they put on you. Look how awesome you are now!

    1. Megan says:

      Oh yeah, especially after the hell I went through and to some extent still going through with my hormone problems.

  6. Tarah says:

    You are amazing! I love your outlook and your determination! It’s beautiful! Kudos to you for saying “No, I’m in charge.”

    1. Megan says:

      Thank you Tarah! I only wish I would had the courage to do is sooner.

  7. Emily says:

    Wow, Megan, I had no idea that you suffered from chronic illness, and this story of overcoming is so amazing. It’s so true that only you really knows what can work with your body, and I’m so glad that you started with the gift of walking. It’s such a gift to live, even with pain; thank you for reminding me of that. <3 You are such an encouragement to many who struggle.

    1. Megan says:

      Thank you sweet Emily. You are amazing as well lady!

      1. Waleska says:

        A person with this kind of problem can have kids?

        1. Megan says:

          As far as I know they can, but you should ask your doctor.

  8. Ellen @ My Uncommon Everyday says:

    GO YOU. Seriously, every day you decide that you win and your chronic condition doesn’t is something to celebrate. This follows a similar trajectory to my story, though mine happened much younger and wasn’t as extreme as the surgery. I was a teenager when I was told that my severe chronic pain was a result of extremely hypermobile joints caused by EDS, and that most EDS patients end up in wheelchairs and on opioids. And I said nope. As long as I make it a point to stay active, the pain I’m in is somewhat manageable, so I’ve grown to love all things fitness. Totally changed my life… and hopefully it gives me a future in which I can still be mostly-normal and engaged with the world.

    1. Megan says:

      Wow, you have your own incredible story Ellen! Thank you for sharing. I think it helps others to know they are no alone and how fitness can heal beyond what we think. Best of luck to you!

  9. Morgan @ Morgan Manages Mommyhood says:

    You have such an amazing story and you are such a fighter!Go you girl. Never let someone else telly ou what you can or can’t do.

    1. Megan says:

      Thank you Morgan! Sometimes I feel like fighter should be my middle name. Haha

  10. Susie @ Suzlyfe says:

    You know that I am a fan, advocate, and proponent of living life on your own terms. Put yourself in the driver’s seat of your own life! I’m definitely glad that you decided to fight for your right to lead a fulfilling and amazing life!

    1. Megan says:

      I know you of all people get this. Hope things are going better for you this week friend.