Juneteenth, Delayed Freedom, and the Fight for Health Equity Today

Juneteenth takes place on June 19th. It is a day to honor the emancipation of the last enslaved Black Americans in Galveston, TX in 1865, more than two years after the Emancipation Proclamation. Throughout June, HealthTree will be sharing information to help raise awareness about disparities in cancer care for Black Americans.
When we think about Juneteenth, we often think about freedom.
But the full story is more complicated than that.
Freedom did not come all at once. It did not reach everyone at the same time. Even after the Emancipation Proclamation was signed, many enslaved people in Texas did not learn they were free until two years later.
Two years.
Not because freedom did not exist, but because the information did not reach them.
That part of the story matters. Because in many ways, we are still living with the consequences of delayed information today.
When information comes too late
In healthcare, especially within Black communities, delayed information is still costing lives.
Patients are often diagnosed later.
They are given limited or unclear information about their condition.
They may not know all of their treatment options or clinical trials.
They are left to navigate complex decisions without the support they need.
Just like in 1865, the issue is not always that help or options do not exist. It is that people do not always receive the information in time to benefit from them.
And when it comes to diseases like multiple myeloma and other blood cancers, timing matters.
Education is more than information, it is power
Knowing what questions to ask.
Understanding your diagnosis.
Being aware of your options.
That is what real education looks like.
At the HealthTree Foundation, education is about making sure patients and caregivers have access to clear, accurate, and meaningful information so they can make informed decisions about their care.
Because when you know more, you can advocate for yourself differently.
And that can change outcomes.
Support changes the journey
A diagnosis can feel isolating.
But no one should have to walk through it alone.
Support means connecting with others who understand, having a space to ask questions without judgment, and learning from people who have been there before.
For many patients, support is the moment things begin to shift. It is where fear starts to turn into clarity and confusion turns into direction.
And for Black patients, culturally relevant support matters. Being seen, heard, and understood is not a luxury. It is necessary.
HealthTree helps you stay connected
Join HealthTree Connect, a social media network for people with cancer, the Black Myeloma Health Facebook Group, or follow us on Instagram to stay in touch.
Research is about representation and access
There is a long and painful history that has shaped how Black communities view medical research.
That reality cannot be ignored.
But what is also true is this: When we are not included in research, we are left out of the solutions.
Clinical trials and research advancements are how new treatments are developed. They are how care improves over time.
Participation is not about being experimented on. It is about being represented.
It is about ensuring that the treatments of tomorrow are effective for everyone, including us.
Freedom today looks different
Freedom today is not just about where you can go.
It is about what you know.
The choices available to you.
The support around you.
And whether you have access to the care you deserve.
Freedom today looks like being diagnosed early, understanding your treatment options, having support throughout your journey, and having a voice in research and innovation.
Moving from awareness to action
Juneteenth reminds us that freedom delayed is not the same as freedom realized.
So the question becomes, what does it look like to make sure information, support, and opportunity are not delayed any longer?
It starts with action.
Learn.
Ask questions.
Connect with others.
Explore your options.
And if you are able, consider how you can be part of advancing research for the future.
Because real change does not just come from awareness. It comes from what we do with it.
When you create a HealthTree account, you can participate in HealthTree research surveys. You can also track your symptoms, monitor your labs, and more!
Sign up now
This Juneteenth, we honor the past by telling the full truth.
And we honor the present by making sure that knowledge, support, and access reach our communities in real time.
Not years later.
Not too late.
Right now.
Juneteenth takes place on June 19th. It is a day to honor the emancipation of the last enslaved Black Americans in Galveston, TX in 1865, more than two years after the Emancipation Proclamation. Throughout June, HealthTree will be sharing information to help raise awareness about disparities in cancer care for Black Americans.
When we think about Juneteenth, we often think about freedom.
But the full story is more complicated than that.
Freedom did not come all at once. It did not reach everyone at the same time. Even after the Emancipation Proclamation was signed, many enslaved people in Texas did not learn they were free until two years later.
Two years.
Not because freedom did not exist, but because the information did not reach them.
That part of the story matters. Because in many ways, we are still living with the consequences of delayed information today.
When information comes too late
In healthcare, especially within Black communities, delayed information is still costing lives.
Patients are often diagnosed later.
They are given limited or unclear information about their condition.
They may not know all of their treatment options or clinical trials.
They are left to navigate complex decisions without the support they need.
Just like in 1865, the issue is not always that help or options do not exist. It is that people do not always receive the information in time to benefit from them.
And when it comes to diseases like multiple myeloma and other blood cancers, timing matters.
Education is more than information, it is power
Knowing what questions to ask.
Understanding your diagnosis.
Being aware of your options.
That is what real education looks like.
At the HealthTree Foundation, education is about making sure patients and caregivers have access to clear, accurate, and meaningful information so they can make informed decisions about their care.
Because when you know more, you can advocate for yourself differently.
And that can change outcomes.
Support changes the journey
A diagnosis can feel isolating.
But no one should have to walk through it alone.
Support means connecting with others who understand, having a space to ask questions without judgment, and learning from people who have been there before.
For many patients, support is the moment things begin to shift. It is where fear starts to turn into clarity and confusion turns into direction.
And for Black patients, culturally relevant support matters. Being seen, heard, and understood is not a luxury. It is necessary.
HealthTree helps you stay connected
Join HealthTree Connect, a social media network for people with cancer, the Black Myeloma Health Facebook Group, or follow us on Instagram to stay in touch.
Research is about representation and access
There is a long and painful history that has shaped how Black communities view medical research.
That reality cannot be ignored.
But what is also true is this: When we are not included in research, we are left out of the solutions.
Clinical trials and research advancements are how new treatments are developed. They are how care improves over time.
Participation is not about being experimented on. It is about being represented.
It is about ensuring that the treatments of tomorrow are effective for everyone, including us.
Freedom today looks different
Freedom today is not just about where you can go.
It is about what you know.
The choices available to you.
The support around you.
And whether you have access to the care you deserve.
Freedom today looks like being diagnosed early, understanding your treatment options, having support throughout your journey, and having a voice in research and innovation.
Moving from awareness to action
Juneteenth reminds us that freedom delayed is not the same as freedom realized.
So the question becomes, what does it look like to make sure information, support, and opportunity are not delayed any longer?
It starts with action.
Learn.
Ask questions.
Connect with others.
Explore your options.
And if you are able, consider how you can be part of advancing research for the future.
Because real change does not just come from awareness. It comes from what we do with it.
When you create a HealthTree account, you can participate in HealthTree research surveys. You can also track your symptoms, monitor your labs, and more!
Sign up now
This Juneteenth, we honor the past by telling the full truth.
And we honor the present by making sure that knowledge, support, and access reach our communities in real time.
Not years later.
Not too late.
Right now.

about the author
Valarie Traynham
Valarie Traynham has been a myeloma survivor since 2015. Wanting to be a source of support, provide patient education and encouragement to help others along their myeloma journey, she is a volunteer myeloma coach, myeloma support group leader and patient advocate. She enjoys being outdoors, reading, and trying new recipes.
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