In lieu of the HealthTree 2.0 Launch Event announced yesterday morning, we wanted to share with you some of the exciting improvements that you will begin to see within our HealthTree Foundation for Chronic Lymphocytic Leukemia.
Our Foundation has grown significantly within the last three years, with many developed programs improving and even more successful programs being developed.
The HealthTree 2.0 Model will consist of 3 core pillars into which all of our programs can be organized.
We believe that by encouraging our community to interact with our programs through these three pillars, patients and caregivers alike will remain empowered, educated individuals who make important connections with their CLL community and participate in key research that leads to a CLL cure.
Today, we will highlight the first pillar of the HealthTree 2.0 Model: Personalized, Lifetime Support and Education.
Several of our programs at HealthTree are geared towards personalized, lifetime support and education. We believe that by empowering CLL patients and their loved ones to learn all that they can about the disease, find specialists who stay on top of the latest and greatest, and become active partners in their care will both live longer and live a higher quality of life.
In fact, we have seen that through the many patients and caregivers that we have helped along the way.
When these empowered members of our community feel supported and have a trusted team to which they can ask their questions, there’s no limit to how involved and active they can be in their own care.
Blood cancer patient Jean Becker shares,
“My first observation when engaging with HealthTree, was that it is patient-centered/focused, so I could access and understand information.
The breadth and depth of resources as well as timeliness (current), is so helpful and supportive. No matter what my questions are, from testing to treatments, to side effects, I can always find answers, information, or a direction.
And if they aren't there, I can ask, and get answers.
The community is so supportive. The range of experts and access to them, and their knowledge through the courses, or regular webinars, chapters, etc. has been crucial to my journey, as I feel prepared to advocate for myself and others with good information and data.”
Our podcast program, in which we interview CLL specialists about their open clinical trials and other hot topics in CLL, was the very first program within our foundation.
Jenny, HealthTree's Founder and CEO, as a patient herself, was having a hard time finding a clinical trial that she qualified for in her area. She decided to take things into her own hands and start interviewing doctors to make it easier for her and others like her to understand clinical trials and know how to sign up for one.
New podcast episodes continue to be released, with many patients claiming this as their favorite educational program.
Part of providing personalized lifetime education includes publishing up-to-date, easy-to-understand information about the latest and greatest in CLL. On our news site, you can read articles about newly approved CLL medications, results of clinical trials, CLL patient stories, and much more.
“The HealthTree Foundation programs have helped keep me up to date on the ever-changing landscape of treatments,” says blood cancer patient Angela Perez, “I can always count on HealthTree to have the latest news on the newest treatments and clinical trials available.”
Our HealthTree webinar program launched in October 2021. The program began in the midst of a global pandemic when many immunocompromised patients and their families had to remain at home.
Different groups were created and called Chapters, in which people could search for webinars based on their interests, the current status of their disease, or their demographic. In CLL, we started broadly with an Adult CLL chapter and a CLL Caregiver chapter. In the future, we plan to open new chapters like various CLL treatment-specific chapters.
We are dedicated to providing personalized education through these webinars and inviting top experts to educate the community on the most crucial CLL topics.
Perhaps our most popular program, HealthTree University has drastically changed the way that the CLL community can educate themselves about complex CLL topics.
The HealthTree University team interviews CLL specialists at conferences and other events to get their expert opinions on questions that matter to CLL patients. The original curriculum was developed by Cindy Chmielewski, a former teacher and blood cancer patient (and also Twitter queen @myelomateacher).
HealthTree Patient Experience Team
In addition to education, we strive to provide support to each of our community members.
Our Patient Experience team, led by Ana Sahagun, consists of a patient navigation and medical navigation team.
The Patient Navigation team can help you find CLL resources, answer questions about our website, and troubleshoot any issues you may have.
Our Medical Navigation team can help you answer questions that you have about CLL (although they cannot give medical advice), aid you in understanding what your personalized lab values mean, and provide insight on general CLL medication questions that you may have.
You can contact them by emailing support@healthtree.org, or calling/texting +1 800 709 1113.
The rest of our website includes many resources such as:
You can explore our website or contact our team if you are looking for specific resources.
At HealthTree, we believe no one should have to face CLL alone.
We encourage you to utilize the programs within Pillar One to educate yourself, your loved ones, and find personalized, lifetime support as you go along your CLL journey. The next step is to become a part of the CLL cure by participating in HealthTree Cure Hub's CLL research.
You can learn about the new and improved HealthTree model, our goals, and how you can be involved in our upcoming HealthTree 2.0 event. Invite your friends & family and join us on October 23, 2023, to hear how you can get your best care and contribute to accelerating a CLL cure.
In lieu of the HealthTree 2.0 Launch Event announced yesterday morning, we wanted to share with you some of the exciting improvements that you will begin to see within our HealthTree Foundation for Chronic Lymphocytic Leukemia.
Our Foundation has grown significantly within the last three years, with many developed programs improving and even more successful programs being developed.
The HealthTree 2.0 Model will consist of 3 core pillars into which all of our programs can be organized.
We believe that by encouraging our community to interact with our programs through these three pillars, patients and caregivers alike will remain empowered, educated individuals who make important connections with their CLL community and participate in key research that leads to a CLL cure.
Today, we will highlight the first pillar of the HealthTree 2.0 Model: Personalized, Lifetime Support and Education.
Several of our programs at HealthTree are geared towards personalized, lifetime support and education. We believe that by empowering CLL patients and their loved ones to learn all that they can about the disease, find specialists who stay on top of the latest and greatest, and become active partners in their care will both live longer and live a higher quality of life.
In fact, we have seen that through the many patients and caregivers that we have helped along the way.
When these empowered members of our community feel supported and have a trusted team to which they can ask their questions, there’s no limit to how involved and active they can be in their own care.
Blood cancer patient Jean Becker shares,
“My first observation when engaging with HealthTree, was that it is patient-centered/focused, so I could access and understand information.
The breadth and depth of resources as well as timeliness (current), is so helpful and supportive. No matter what my questions are, from testing to treatments, to side effects, I can always find answers, information, or a direction.
And if they aren't there, I can ask, and get answers.
The community is so supportive. The range of experts and access to them, and their knowledge through the courses, or regular webinars, chapters, etc. has been crucial to my journey, as I feel prepared to advocate for myself and others with good information and data.”
Our podcast program, in which we interview CLL specialists about their open clinical trials and other hot topics in CLL, was the very first program within our foundation.
Jenny, HealthTree's Founder and CEO, as a patient herself, was having a hard time finding a clinical trial that she qualified for in her area. She decided to take things into her own hands and start interviewing doctors to make it easier for her and others like her to understand clinical trials and know how to sign up for one.
New podcast episodes continue to be released, with many patients claiming this as their favorite educational program.
Part of providing personalized lifetime education includes publishing up-to-date, easy-to-understand information about the latest and greatest in CLL. On our news site, you can read articles about newly approved CLL medications, results of clinical trials, CLL patient stories, and much more.
“The HealthTree Foundation programs have helped keep me up to date on the ever-changing landscape of treatments,” says blood cancer patient Angela Perez, “I can always count on HealthTree to have the latest news on the newest treatments and clinical trials available.”
Our HealthTree webinar program launched in October 2021. The program began in the midst of a global pandemic when many immunocompromised patients and their families had to remain at home.
Different groups were created and called Chapters, in which people could search for webinars based on their interests, the current status of their disease, or their demographic. In CLL, we started broadly with an Adult CLL chapter and a CLL Caregiver chapter. In the future, we plan to open new chapters like various CLL treatment-specific chapters.
We are dedicated to providing personalized education through these webinars and inviting top experts to educate the community on the most crucial CLL topics.
Perhaps our most popular program, HealthTree University has drastically changed the way that the CLL community can educate themselves about complex CLL topics.
The HealthTree University team interviews CLL specialists at conferences and other events to get their expert opinions on questions that matter to CLL patients. The original curriculum was developed by Cindy Chmielewski, a former teacher and blood cancer patient (and also Twitter queen @myelomateacher).
HealthTree Patient Experience Team
In addition to education, we strive to provide support to each of our community members.
Our Patient Experience team, led by Ana Sahagun, consists of a patient navigation and medical navigation team.
The Patient Navigation team can help you find CLL resources, answer questions about our website, and troubleshoot any issues you may have.
Our Medical Navigation team can help you answer questions that you have about CLL (although they cannot give medical advice), aid you in understanding what your personalized lab values mean, and provide insight on general CLL medication questions that you may have.
You can contact them by emailing support@healthtree.org, or calling/texting +1 800 709 1113.
The rest of our website includes many resources such as:
You can explore our website or contact our team if you are looking for specific resources.
At HealthTree, we believe no one should have to face CLL alone.
We encourage you to utilize the programs within Pillar One to educate yourself, your loved ones, and find personalized, lifetime support as you go along your CLL journey. The next step is to become a part of the CLL cure by participating in HealthTree Cure Hub's CLL research.
You can learn about the new and improved HealthTree model, our goals, and how you can be involved in our upcoming HealthTree 2.0 event. Invite your friends & family and join us on October 23, 2023, to hear how you can get your best care and contribute to accelerating a CLL cure.
about the author
Audrey Burton-Bethke
Audrey is an editor for the HealthTree Foundation. She originally joined the HealthTree Foundation in 2020 as the Myeloma Community Program Director. While not knowing much about myeloma initially, she worked hard to educate herself, empathize, and learn from others' experiences. She loves this job. Audrey is passionate about serving others, loves learning, and enjoys iced chais from Dutch Bros. She also loves spending time with her supportive husband and energetic three-year-old.
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