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Fighting Cancer Is Hard. 15 Tips for Living With Chronic Illness
Posted: May 26, 2017
Fighting Cancer Is Hard. 15 Tips for Living With Chronic Illness image

BY KIM GILES Find the original article on KSL.  CC Scott said, “The human spirit is stronger than anything that can happen to it.” I believe this is true, so the first thing I want you to know is that you can have joy in spite of this, and you can beat discouragement most of the time. I say “most of the time" because every once in a while it is perfectly normal to have a big old pity party about your pain or illness. I do. I have been diagnosed with Sjogrens syndrome and it's not fun. Chronic illness is tough and it gets discouraging. An occasional fall apart day (or hour) or week is totally acceptable - but you can’t live there. After you give yourself the chance to mourn, which you will do, because "loss of health" is a loss, you must choose a positive, determined, healthy mindset so you can thrive in spite of the challenge. Vivian Green said, “Life isn’t about waiting for the storm to’s about learning to dance in the rain.” For many of us, the storm isn’t going anywhere, so we need to start dancing.

I asked some other people I know who are battling chronic illness to help me with this article partly because I wanted some more advice on this, too. Hopefully, their ideas will help you as much as they've helped me. Here are our suggestions for making it through chronic illness with as much joy as possible:
You must make self-care your top priority. If you don’t, you will have nothing to give anyone else. Whether it’s sleep, exercise, eating right, doing less, getting massages or taking naps - do what you need every day.
Set very realistic goals, but have some kind of project or goal you are working towards. Accomplishing even small things will increase your satisfaction and joy.
Understand that illness is not a sign of weakness or a personal failing. Do not blame yourself for being sick. Toni Bernhard, author of the book How To Be Sick, writes ”I blamed myself – as if not regaining my health was my fault, a failure of will, somehow, or a deficit of character. This is a common reaction for people to have toward their illnesses. It’s not surprising, given that our culture tends to treat chronic illness as some kind of personal failure on the part of the afflicted.” You cannot buy into this. You must know the truth and see this experience accurately.
Understand this illness is just a class in your life to teach you something. Life is a classroom and if "health problems" is your current class, there is a reason you are here. There is something that this experience can teach you that you apparently need to learn. If you see your illness as a class and focus on the character development it could bring you, it will change the way you experience it. Khalil Gibran said, “Out of great suffering has emerged the strongest of souls; the most massive characters are seared with scars.” This is truth. Suffering builds character and compassion and in the end it makes you stronger and better. If you focus everyday on how your current experience could improve your character or allow you to help other people, you will suffer less - I promise. Viktor Frankl said, “In some way, suffering ceases to be suffering at the moment it finds a meaning." This is profoundly true. Try it.
Don’t let the fact that others don’t have "chronic illnesses" get to you. "Miraculously recover or die is the extent of our cultural bandwidth for chronic illness," according to S. Kelley Harrell, and I agree. People just don’t know what to do when they can’t say “get better soon.” When there is no getting better, they don’t know what to say. Don’t be offended by this. Just let them be where they are and know they really do care. (If you want to know the right thing to say to someone suffering with chronic illness try, “I love you, sorry you have to go through this, you’re in my prayers," or, "You are so strong and it’s really inspiring!”)
Find a support system with other people who are in the same boat. It really helps to have people in your life who do get it and can offer encouragement and suggestions.
Don’t own the chronic illness and make it your identity. Avoid saying things like “it’s my lupus.” Just say, “It’s lupus.” There is a difference and it does matter. You are much more than just this challenge and it does not define you. You are much more than this experience.
Keep moving as much as you can. My friend Alex has Parkinson’s disease and he recommends walking, biking, tai chi or whatever you can do to keep moving, because exercise produces endorphins, which feel great. They also improve mood and help your immune system. I would add getting out in nature as much as you can, too. It does me a world of good.

One of my favorite quotes by Marcus Aurelius says, “You have power over your mind – not outside events. Realize this, and you will find strength.” Often in life we have no control over our situation, but we always have control over how we will experience the situation. To help me control how I experience illness I read something three times a day to keep me centered in the mindset I’ve chosen. You can download my reading here. Feel free to tweak it to make it work for you. Then read it three times a day until you internalize it. You can handle this and thrive! Kimberly Giles is the founder and president of She is also the author of the new book "Choosing Clarity: The Path to Fearlessness" and a popular life coach and speaker.  

The author Jennifer Ahlstrom

about the author
Jennifer Ahlstrom

Myeloma survivor, patient advocate, wife, mom of 6. Believer that patients can help accelerate a cure by weighing in and participating in clinical research. Founder of Myeloma Crowd by HealthTree and the HealthTree Foundation.

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