Cheryl is sitting cross legged on the ground with a serious facial expression, looking at an array of medication bottles and syringes which are used to manage my chronic illnesses including rheumatoid arthritis, gastroparesis, cervicalgia, whiplash and more.
Editor Update 2025: This post was originally published on Cheryl’s blog, The Enthusiastic Life, and then republished here with her permission. Today, Cheryl runs the amazing resource Arthritis Life – if you live with any type of arthritis, we highly recommend checking out what she has to offer! You can find her on Instagram, YouTube, and Facebook.
People often remark that those of us with invisible illnesses “don’t look sick.” However, we deal with substantial physical and emotional challenges. To shed light on the often hidden side of living with chronic illness, I completed an “Invisible Illness Photo Shoot” with dear friend and phenomenal photographer Jessica Keener Photography.
Goals of the photo shoot
I have many good days, like the one on the left. I also have hard days, as shown on the right.
1. To illustrate that you cannot tell what someone is going through just by looking at them. I hope that these photos help people remember to “be kind, for everyone you meet is fighting a hard battle” (Ian MacLaren).
2. To help those who have similar invisible challenges not feel alone. I have benefited from seeing other brave chronic illness warriors share their trials and triumphs, and I wish to add my contribution.
3. To visually express that life with multiple chronic illnesses contains many “good days” and “bad days.” As a positive person (my entire blog is called “The Enthusiastic Life,” after all!), I typically favor sharing photos of good days. However, I also wish to show the truth of my life, and I experience many “bad days” along with the good.
The photos are available below. Please feel free to share this post or individual photos for educational reasons, but I ask that you:
Injecting one of my two weekly injected medications for rheumatoid arthritis: Orencia. Image credit: Jessica Keener Photography
The photo description at the top says it all. When you already have multiple chronic health issues, adding an acute health issue such as a car accident is really difficult. Image credit on the bottom: Jessica Keener Photography
Photos of the social and emotional aspects of chronic illness: my role as a friend, wife and mother
On good days, you will see my smiling face. I love sharing photos on my good days! However, I often don’t have the energy or interest in sharing my bad days, so they are even more hidden. What is actually happening on a bad day is shown in the photo at the bottom: usually rest, pain management, missing out on fun things in life, and isolation. Image credit: Jessica Keener Photography.
On top, my husband and I are admiring on rings on our wedding day. On the bottom, my ring is in clear focus as I inject one of my two weekly injected medications. Image credit on top: Cory Parris Photography. Image credit on bottom: Jessica Keener Photography.
This composition was directly inspired by Kathy DiVincenzo’s powerful photo, taken by Danielle Fantis, of her on a good day versus bad day after postpartum depression. Image credit: Jessica Keener Photography.
My husband plays athletically with Charlie in the style I always imagined myself playing before I got sick. On the bottom, in contrast, is me on a “bad day.” Image credit: Jessica Keener Photography.
“Some owies don’t get better” – chronic, lifelong illness is really difficult to explain to small children. In this photo, Charlie helps me put band-aids on one of my injection sites for my weekly rheumatoid arthritis medication.Image credit: Jessica Keener Photography.
It’s hard to put into words or images how difficult it was to decide whether to try to have another biological child. Image credit: Jessica Keener Photography.
In 2016, I had surgery to remove a pilonidal cyst. I experienced delayed wound healing for months afterwards. So many doctors referred to me as a “slow healer” that it became an inside joke between my husband and I. The letters are written on the same sized bandages that my husband had to change 3 times a day for 6 months. Image credit: Jessica Keener Photography.
Cheryl Crow is an occupational therapist (OT) who is passionate about helping others live their lives to the fullest despite chronic illness or disability. She has had rheumatoid arthritis and gastroparesis for 15 years and volunteers to perform patient education with the Arthritis Foundation. She works as a community college instructor in a OT Assistant program as well as in pediatrics. She shares personal stories, OT tips and life hacks for living with arthritis on her blog The Enthusiastic Life.