the IBC network foundation

EDUCATION  +  RESEARCH  +  SUPPORT

No Lump… Still Cancer

Over $1.9 million donated to inflammatory breast cancer research by The IBC Network Foundation.

We also attend research meetings, serve on grant committee’s, advocate, educate and run online support groups, just to list a few ways we spend our time. 

However, we are intensely focused on funding high quality research, because we feel research matters.

What is IBC?

Inflammatory Breast Cancer (IBC) is a rare and very aggressive disease in which cancer cells block lymph vessels in the skin of the breast.

This type of breast cancer is called “inflammatory” because the breast often looks swollen and red, or “inflamed”.

OUR MISSION:

  • To fund research regarding Inflammatory Breast Cancer.
  • To provide an avenue to network proactive education to the general population as well as the medical community regarding Inflammatory Breast Cancer.

 

It is important to know how your donation is utilized. The IBC Network Foundation existence is to fund research to eradicate this disease. We are a 501c3.

REGISTRATION IS NOW OPEN!

Symptoms, Facts & Statistics

Inflammatory breast cancer defined, read the symptoms IBC may include and discover the facts and stats about IBC you need to know.

Treatment Centers

Just like IBC presents differently and has different diagnosis needs, the standard of care is different from general forms of breast cancer. Due to the rarity of the disease, IBC diagnosis and treatment is not commonly taught in medical or nursing schools.

Shop the IBC Network Store and make a difference!


Every purchase supports inflammatory breast cancer research, advocacy, and education. Your shopping helps fuel hope, fund progress, and move us closer to a future where IBC is a disease of the past. Thank you for supporting the mission!

IBC LEARNING ACADEMY

The IBC Learning Academy is a rigorous course with the objective of training devoted Inflammatory Breast Cancer advocates. Trained advocates will be empowered to promote the unique needs of IBC patients by improving access to specialty care, increasing education around clinical trials, and participating in lobbying. 

TALK IBC PODCAST

The Talk IBC Podcast is where we will discuss things related to inflammatory breast cancer, from patient’s personal stories to the latest in research. A new episode will be released every two weeks as Terry Arnold interviews new guests. 

Walking on Quicksand Magazine

Walking on Quicksand is an online magazine that shows that life persists post-diagnosis. This is a place to showcase the fullness of ourselves, beyond the label of a person who lived with or during the time they lived with cancer. We are now accepting article submissions.

The mission of the IBC Network Foundation is dedicated specifically to fund medical research for inflammatory breast cancer.

The following graphic reflects why our mission is so needed.
This shows breast cancer grants over the last 20 years. *

breast cancer grants

ARTICLES

The New Normal

People have mentioned I have been awfully quiet lately. I suppose that’s because sometimes I just don’t know what to say. I got those amazing clear scans - cancer free! - and then the chorus of comments began: “Aren’t you excited, you’re done!” “You beat it!” “You...

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I’ll keep this short

When I first see you or meet you for the first time, please don't tell me that your beloved mom/sister/aunt/best friend died of cancer. Folks, when you are fighting the disease, this gets old. "You take chemotherapy for breast cancer? My sister in law did. She died...

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Announcing the Inflammatory Breast Cancer Ribbon!

Drum roll please......I know you're all wishing to know about the IBC #ribbon. A little background: The Inflammatory Breast Cancer community has long wished for a ribbon that was unique for this subset of breast cancer.  Requests from women and men with IBC, mirroring...

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A few ways we have helped…

“Education from the IBC Network Foundation, I think was truly part of me becoming, finally, NED through treatment.”

– Eva

“When I was first diagnosed, they told me that they would never call me cured, but that it would just be called NED. Somehow within the past couple of years, it’s changed. They told me that after 7 years, they would consider me cured. Times are changing, things are changing. There is hope.”

Chrisanne

“…having the knowledge and evidence based materials at my fingertips has really been beneficial in the steering of my treatment. My oncologist, my team, has been fantastic at following that evidence base, but actually knowing what I should be expecting and knowing how to advocate for myself has been the most important piece of my treatment plan and The IBC Network Foundation has really given me two legs to stand on when it comes to being in charge of my own treatment plan”

– Kristin

“…I’m very appreciative of The IBC Network and Terry Arnold, and this whole community. We are truly better together. It’s amazing to have a network of people to lean on.”

– Julie

“The IBC Network Foundation made a huge difference for me. They helped me find the right treatment after the initial hospital did not want to do radiation and surgery since I was stage 4 already. I had surgery and radiation, finished in July 2019, and have been NED since.”

– Jill

“I would not have been diagnosed as quickly as I was if I hadn’t had the information and resources that The IBC Network provides us on their website and their app.”

– Erin

“I’ve gotten a lot of support and questions answered from The IBC Network Foundation. If it wasn’t for them, I probably wouldn’t have been connected to MD Anderson, I would not have been able to take part in the clinical trial that I was able to take part in. So I’m very thankful. We are both doing amazing.”

– Kelly

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