Lymphedema Advocate – Process to Progress Dominique Rogers | Juzo USA
March 2021

Lymphedema Advocate – Process to Progress Dominique Rogers

Tom Musone, Director of Marketing

Career fire fighter, EMT and fitness enthusiast is our newest Juzo Champion

In honor of Lymphedema Awareness Month, we’re excited to introduce the newest member of the extended Juzo family, Dominique Rogers. After quietly living for lymphedema for more than a decade, he decided to share his story to help advocate for others. His story and motto, “Process to progress” is as inspiring as his fitness regime. Keep reading to get to know him a little better and welcome him in the comments below!

Tell us a little about yourself.
I’m 32 years old and from Hartford, CT. I have four brothers, one sister and 12 nieces and nephews. I’ve enjoy running on the track, photography and videography. In the summer, I play flag football.

When were you diagnosed with lymphedema?
I was diagnosed with lymphedema in 2005, when I was 15. I was outside playing basketball and rolled my ankle. It started to swell. When I got home, my mom told me to elevate it and put ice on it. The next day, my whole leg was swollen. After a week in the hospital, I was diagnosed with lymphedema.

What are some misconceptions others have about lymphedema?
Many people think that lymphedema is a form of cancer.

Why is it important to raise awareness of this condition?
It’s important to raise awareness for lymphedema because many people don’t know they have the disease. People that do have the disease feel alone, sometimes, because others don’t understand what they are going through.

How are you able to live such an active lifestyle?
I’m able to live an active lifestyle due to my consistency in what works for me in maintaining my lymphedema. I wear my compression garment every day and go to therapy. Also, I get up early and workout. every day. I eat as healthy as I can by staying away from salty foods.

Who is your inspiration?
My mother Charlotte Rogers. She is the strongest women I know, full of joy and willing to help others, whenever they need it. She’s very giving and supportive of me and my siblings. My mom and I grew a deeper bond when she was diagnosed with breast cancer and later lymphedema. We had each other’s backs, maintaining the disease together. My mother and father are the reason on who I am today and why I will continue to motivate people, with or without the disease, to keep pushing forward.

Why did you get involved in the lymphedema advocacy community?
I got involved because I felt like it was time. I’ve been cruising along quietly with this disease for over a decade. I’ve been through a lot in my life and came out on the other side. I’ve gone from being in the hospital two times a year, due to an infection in my leg, to where I am now – a career fireman and an EMT. It was a Process to Progress, and I want to help others who are like me. If my story can help someone get through the day and realize they’re not alone and they can do anything they put their minds to…I would be happy with that.

What words of inspiration or motivation do you have for others with lymphedema?
Everything takes time. Everything is a process.

Learn more about Dominique and following his inspirational lifestyle at his new website: process2progress.com. Follow him on Instagram @theprocess2progress.


Be to follow us on Instagram, @JuzoCompression and Facebook to learn more about how Juzo supports the lymphedema community. Meet other Juzo Champions and find out more about lymphedema at Juzousa.com.

Sheila commented on Jul 14, 2023
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I have had lymphedema in my left leg for 46 years happened the exact same way. I was playing basketball rolled my ankle and my leg progressively swelled up. Diagnosed with primary lymphedema. I would very much like to become an advocate for people with our condition especially when it comes to getting help with the cost of therapy and compression garments. Please respond.

Amika commented on Apr 22, 2023
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Thank you for sharing your motto of "Process to Progress". Very encouraging to me.

Gloria Brown commented on Mar 25, 2023
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I have stage 2 lymphadema and have gone to the clinic. I am trying to embrace the disease but I still fill ashame showing my legs in dresses. I believe mine came from a hysterectomy surgery and a nerve was hit.

Judy Peters commented on Mar 22, 2023
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Thanks for sharing!

Davine G. Bundridge commented on Mar 20, 2023
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I have been diagnosed with lymphedema and it has been some type of journey, for which I first noticed something like a blister...so, I was back and forth at the Wound Clinic for sometime...

Roberta Robinson commented on Mar 12, 2023
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I had breast cancer and 10 years later i was diagnosed with lymphedema in my left arm. I do an hour massage therapy by machine and then exercises. Ive had it about 2 1/2 years now. I also wear a compression sleeve and glove. Thanks for tell ur story. Take care

Nichole commented on Mar 10, 2023
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Thank you for sharing your story and transparency. Lymphedema is not talked about enough. I will share your story with a family member who was diagnosed as well.

Beverly Dinofer commented on Mar 10, 2023
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As a MLD therapist your story is inspiring and I hope many people will see and feel good about themselves. Thanks for sharing.

Gennelle commented on Mar 04, 2023
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Thank you for sharing your story.

Tracey commented on Mar 02, 2023
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Thank you for sharing your story being a male also that was very inspiration I just diagnosed with it and needed to hear from others that deal with condition

Shonda Creswell commented on Jun 17, 2022
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Thank you for your comment. It will help me motivate myself a little more.

 
 

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