The National Bone Marrow Transplant Link

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The National Bone Marrow Transplant Link Welcome to our page! nbmtLINK is dedicated to educating and supporting those that are on a

The nbmtLINK is an independent, nonprofit organization funded entirely through the generosity of individuals, corporations, and foundations. Tax-deductible contributions are welcomed and enable us to create and sustain programs and services.

11/09/2026
To register, go to https://pburkhard.wufoo.com/forms/z1ifnw2w18y6g4w/Writing Workshop with Brad BuchananSpecial thanks t...
11/07/2026

To register, go to https://pburkhard.wufoo.com/forms/z1ifnw2w18y6g4w/

Writing Workshop with Brad Buchanan

Special thanks to our sponsors: Blood Cancer United and Sanofi as well as our esteemed Link Partners who are helping to make this program possible. The are listed on our website on the home page.
This workshop will be on Zoom. Here is the link https://zoom.us/j/9579706011?pwd=TzN5MVE2MlJ4UDIrVXcvYUN3UmhuUT09.

A reminder email will be sent the day of with the link as well.(Please refer to yourself on the Zoom as you feel comfortable re: your full name vs. first name.)

WHEN: Wednesday. November 11, 2026, from 1:00pm EST to 2:00 pm EST
12-1pm CST
11am-12pm MST
10-11am PST

Writing is a self-healing activity. This workshop will provide a safe
space to express yourself. We will offer participants a prompt to
write about, time to write and share if they choose, and time to
receive only positive feedback on their writing.

This free activity, led by survivor and writer Bradley Buchanan and facilitated by licensed staff social worker, Jennifer Gillette will surely help survivors feel less isolated, and offer healing connections and comfort.
If you have any questions, please contact Jennifer Gillette, LMSW ([email protected]) or Peggy Burkhard ([email protected]) at the nbmtLINK.

To register, go to https://pburkhard.wufoo.com/forms/z1tmcx371xruuo3/Relationships After Transplant-Focus on CaregiversA...
11/06/2026

To register, go to https://pburkhard.wufoo.com/forms/z1tmcx371xruuo3/

Relationships After Transplant-Focus on Caregivers
A FREE Call In Telephone Support Program for Patients and Their Families/ Caregivers/ Loved Ones
Presented by the National Bone Marrow Transplant Link, www.nbmtlink.org

Special thanks to our generous sponsors:, Mesoblast, Blood Cancer United, Sanofi and Incyte. We also thank our Esteemed Link Partners.
Wednesday, November 18, 2026
Noon to 1 pm EST
Please note these other time zones if applicable:
(11 am CST, 10 am MST or 9 am PST)

*IMPORTANT* YOU MUST CALL IN- please write this down and save it for the day of the program
Here are the Call In Details
Toll Free Dial In: 888-596-4144
Conference ID 7762288 and then press #
Join us for this month's call-in program featuring Christina Ferraro, MSN, APRN-CNP, APP Manager of Outpatient Hematology/Oncology and Director of Survivorship for Cleveland Clinic's Blood and Marrow Transplant and Cellular Therapy Program.

Christina will explore how the caregiver role evolves after transplant, including changes in responsibilities, identity, relationships, and daily life. She will also discuss sexual health, intimacy, and navigating changing relationships with family and friends throughout survivorship.

We also welcome caregiver Brittany Mitchell, who will share her family’s personal journey and the lessons learned along the way. Jennifer Gillette, LMSW, our host, will provide practical coping strategies and professional insights to help patients and caregivers navigate life's challenges after transplant. Bring your questions. There will be plenty of time for live discussion and audience participation.

If you have any technical issues related to registering, please email [email protected] or call (248) 770-5172. The call-in information is contained in the form you use to register. Note: YOU call in TO participate. (We do not call you.) This program is recorded and transcribed and available on our website within one week after airing live. (www.nbmtlink.org)

This FREE program is intended to provide psychosocial and emotional support along with health information from national experts regarding critical topics surrounding cancer and treatments. Jennifer Gillette, our licensed staff social worker, will host this call. There will be plenty of time for live questions.

To ask a question during the Q & A portion of this program, once the operator says the lines have been opened, hit the star key on your phone and then the number 1. Please address yourself when asking a question in the best way to protect your identity if desired.

On Purpose, For Purpose: Why I AdvocateBy Amanda BrunsonWhen I think about advocacy, I don’t simply think about speaking...
11/06/2026

On Purpose, For Purpose: Why I Advocate

By Amanda Brunson

When I think about advocacy, I don’t simply think about speaking on a stage, sitting on a panel, walking the halls of Capitol Hill, or sharing my cancer story. Advocacy, to me, is deeply personal. It is what I have chosen to do with the life I fought so hard to keep.

I was first diagnosed with leukemia at 21-years-old and faced cancer again at 25. Eventually, my journey included a bone marrow transplant. Cancer changed the direction of my life in ways I could never have anticipated. It interrupted my education, affected my fertility, challenged my relationships, changed the way I saw my body and my future, and forced me to confront questions most young adults never expect to face.

There is the fight to survive cancer, but then there is another journey that begins afterward: learning how to live after everything has changed.

For young adults especially, cancer can place what feels like a delay or a pause on life. Temporary is the key word, temporarily. While our peers may be building careers, finishing school, developing relationships, gaining independence, and learning the everyday skills that naturally come with growing older, we may be learning treatment schedules, medications, medical terminology, insurance, and how to make incredibly grown-up decisions at a very young age. In some ways, cancer forces you to grow up faster than you ever should have to, while simultaneously delaying some of the ordinary experiences that help you grow into adulthood. And when treatment ends, there can be an unspoken expectation that you simply pick up where you left off. But acclimating to life again, developing some of the skills you may not have had the opportunity to develop, and finding your place among peers whose lives continued moving forward can have an impact too. I believe that part of the young adult cancer experience deserves to be talked about.

That part of survivorship is one of the reasons advocacy means so much to me.

I know what it feels like to be grateful to be alive while simultaneously trying to figure out what life looks like now. I know what it means to survive physically and still have emotional, financial, medical, and personal pieces that need healing.

I also know what it means to discover that a life changed by cancer can still be a beautiful life. Not an easy life, and certainly not an easy path to walk as you learn to acclimate to your new normal, but it can still be a beautiful life.

I wear a bracelet on my arm that says, “Dreams become reality one choice at a time.” I carry those words with me because rebuilding your life after cancer really does happen one choice at a time. You may not get to choose what happened to you, but you can choose what you do next. You can choose to keep dreaming. You can choose to keep showing up. You can choose to build something meaningful with the life in front of you.

For me, that means choosing purpose. It can be a life full of purpose.

That realization has shaped the way I advocate. I often say that I do things on purpose, for purpose, to bring purpose and ignite purpose in other people.

Those words are more than a saying to me. They are how I try to live.

My advocacy has allowed me to serve as an Adolescent Young Adult (AYA) Ambassador and Patient Peer Advisor at Moffitt, where I mentor and connect with other people affected by cancer, participate in AYA conferences and panels, support bone marrow donor awareness through NMDP, work alongside organizations such as Stupid Cancer, and advocate with Blood Cancer United. It has also taken me to Capitol Hill, where I have had the opportunity to help bring the needs and experiences of cancer patients and survivors directly to people involved in shaping policy.

But the titles and opportunities are not the most important part.

The person is.

It is the young adult sitting in a hospital room wondering whether anyone understands what they are losing while everyone else is focused on keeping them alive.

It is the survivor who rings the bell or finishes treatment and discovers that everyone expects life to simply return to normal.

It is the patient worried about fertility, mental health, finances, chronic side effects, relationships, employment, or what their body may experience years after treatment.

It is the person who needs to hear, “I understand. I have been there too.”

Those are the people I carry with me when I advocate.

Research is also deeply personal to me because I understand that I am alive today because people before me advocated, participated in research, donated bone marrow, developed treatments, funded programs, and believed patients like me deserved a future.

Medical research gave me more than survival. It gave me birthdays I might not have had. It gave me time with the people I love. It gave me the opportunity to rebuild a life.

Because others helped create a path for me, I feel a responsibility to help create a path for someone else.

My faith has also taught me that purpose does not always come from the circumstances we would have chosen. Sometimes purpose grows from the very places that once caused us pain. I would never have chosen cancer. I would never have chosen the losses that came with it. But I can choose what I do with what happened to me.

And I choose to use it. I choose to speak. I choose to show up.

I choose to tell the truth about survivorship, not to diminish the incredible gift of being alive, but because being alive should include having the resources and support necessary to truly live.

Amanda Brunson Blog Contributor
Even after treatment ends, the fight does not end for everyone. Some patients and survivors continue fighting for their lives because of the long-term and late effects of the very treatments that helped save them. Treatment can leave lasting effects on the body and mind, and unfortunately, some survivors lose their lives to complications that develop after cancer treatment is over. That reality is another reason we are asking people to listen, to support research, and to continue helping us even in survivorship.

Every stage of the cancer experience matters, from diagnosis, to active treatment, to everything that comes afterward. But survivorship deserves particular attention because it does not have a clear ending. For many of us, survivorship follows us for the rest of our lives. Our medical needs may change, our bodies may change, and new late effects can appear years later. We need continued research, resources, monitoring, education, and support so that surviving cancer does not simply mean being alive but having the opportunity to live as healthy and full a life as possible.

That is why I advocate for long-term survivorship care, mental health support, fertility preservation, research, financial protection, quality of life, and making sure AYA patients have a voice in decisions being made about their care.

Advocacy has also taught me that purpose does not have to look enormous. Sometimes advocacy happens on Capitol Hill. Sometimes it happens on a stage. And sometimes it happens quietly between two survivors when one person realizes, for the first time, that they are not alone.

All of it matters.

Today, I understand that my story is not only about what I survived. It is about what I am doing because I survived.

Cancer absolutely changed my life. A bone marrow transplant changed my life. There are parts of my story I would never have written for myself. Yet somehow, through all of it, I have been able to build a life that is meaningful, intentional, and full of purpose.

And now I want other people to know they can build one too.

That is what advocacy means to me.

I survived, but I don’t want survival to be where my story ends.

I want to use the life I have been given to make someone else’s journey a little less lonely, to push for changes that make survivorship better, and to remind people that even after life changes completely, there can still be something beautiful ahead.

I want my life to say: Do it on purpose. Do it for purpose. Bring purpose with you and ignite it in someone else.

💙 MYELOMA COMMUNITY WORKSHOP — FREE VIRTUAL EVENT!What's the Right Answer? Controversies in Myeloma📅 Monday, November 16...
11/05/2026

💙 MYELOMA COMMUNITY WORKSHOP — FREE VIRTUAL EVENT!

What's the Right Answer? Controversies in Myeloma

📅 Monday, November 16, 2026
🕕 6:00 PM Eastern | 3:00 PM Pacific
💻 Virtual & FREE!

When it comes to multiple myeloma treatment, there isn't always one clear answer.

Join the International Myeloma Foundation (IMF) for an engaging discussion as leading myeloma experts debate important treatment questions:

🔹 Should all high-risk smoldering myeloma patients receive treatment?

🔹 Is stem cell transplantation still the standard of care for all eligible patients?

🔹 Should maintenance therapy be limited to two years for most patients?

Hear both sides of these important questions from Dr. Joshua Richter and Dr. Doris Hansen, with Dr. Joseph Mikhael opening the program.

Whether you're a patient, survivor, caregiver, or healthcare professional, this workshop offers an opportunity to better understand evolving treatment approaches and make more informed decisions with your healthcare team.

✅ Register FREE:
https://www.myeloma.org/event-register/imf_v_mcw_right_answer_2026

Presented by the International Myeloma Foundation (IMF).

11/05/2026

Caregivers, this one’s for you💙

Just in time for National Family Caregivers Month, we’re releasing the Cancer Caregiver Companion, a free guide on how to take care of yourself when you’re caring for someone else.

It’s honest about the hard parts and makes room for the moments of joy. You’ll find a roadmap of what to expect at each stage, help with burnout and big emotions, realistic self-care ideas (think small!), and words of encouragement from Caregiver Mentor Angels who have been there.

You matter, too. You don’t have to do this alone.

📲 Download it free: https://imermanangels.org/document/cancer-caregiver-companion/
Share it with a caregiver who needs to hear this today.

This activity is supported by an independent educational grant from Genmab.

Address

2900 Union Lake Road Suite 213
Commerce, MI
48382

Opening Hours

Monday 8am - 5pm
Tuesday 8am - 4pm
Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm

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