Young Adults Living
with Chronic Illness
Virtual Support Group
START DATE
Sunday
September 20, 2026
END DATE
Sunday
November 15, 2026
TIME
7:30-8:45 pm
Eastern Standard Time
DURATION
8 weeks, closed group
1 week break partway through
FORMAT
Confidential virtual sessions
Therapist-led
COST
$25 per session, pay-as-you-go
Some insurances accepted
A place to connect with people who
understand what it is like
to navigate chronic illness in young adulthood.
Being a young adult with a chronic illness can feel like you are living a very different life than the people around you. While friends may be building careers, making plans and moving through milestones, you may be balancing appointments, symptoms, medications and the uncertainty of not knowing how you will feel tomorrow.
Even people who care deeply about you may not fully understand what that experience is like.
This group was created for that reason.
Every group is a little different because the conversations are shaped by the people in the room. What stays the same is the sense of relief that often comes from talking with people who simply understand.
Shannon Schureman, LMHC
meet your group facilitator
I understand this experience personally. I was diagnosed with chronic illness as a young adult and know how isolating it can feel to navigate changing health, an uncertain future and a life that may look different than you expected.
Over the past several years, I have facilitated this seasonal support group for young adults living with chronic illness. This group grew out of a desire to create the kind of space I wish had existed when I was first learning how to navigate my own health challenges.
As the facilitator, I help guide conversations and introduce themes that often come up when living with chronic illness. My clinical background informs how I facilitate, including approaches such as Acceptance and Commitment Therapy (ACT), Motivational Interviewing and compassion-focused principles. These approaches help support reflection and meaningful conversation, but the group itself is centered around peer connection.
What To Expect
Each group session begins with a brief check-in to help everyone settle in. From there, we move into a discussion topic that reflects the experiences and interests of the group.
Common Topics of Discussion
Identity Changes and Self-Discovery
Processing how illness can shape a person’s sense of self.
◈
Navigating the Medical System
Sharing experiences with accessing care and communicating with providers.
◈
Relationships and Support Systems
Exploring the role of connection and understanding in relationships.
◈
Dating and Intimacy
Discussing how chronic illness affects romantic relationships and closeness.
◈
Ableism and Disability Experiences
Examining the impact of disability-related stigma and misunderstanding.◈
Work and Productivity
Exploring changing relationships with achievement and personal expectations.◈
Body Trust and Body Grief
Processing changes in the relationship with one’s body.
◈Coping and Self-Care
Discussing ways to support oneself while living with chronic illness.◈
Hope and Acceptance
Exploring how to hold space for uncertainty while moving forward.
No one is expected to have the right answers. The value comes from hearing different perspectives and realizing you are not the only person asking these questions.
This is not a group where people need to come prepared with solutions. Many people living with chronic illness already receive plenty of advice they did not ask for. This group focuses on listening, sharing experiences and offering support that comes from feeling understood.
This group is built around respect, curiosity and understanding. Everyone's experience with chronic illness is different. Members are encouraged to share their own experiences while recognizing that what works for one person may not work for another.
Interested in Joining?
I would love to hear from you!!
If you are interested in joining the next group, please complete the brief screening survey using the button below. It only takes a few minutes and no login or sign-up is required.
After I receive your responses, I will reach out to answer any questions and talk with you about whether the group feels like a good fit.
If filling out a form is not your thing, you are welcome to reach out instead. I am happy to schedule a brief phone call.
Group FAQs
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The group is intended for adults in their 20s and 30s. If you're just outside that range, feel free to reach out. Depending on the group, there may be some flexibility.
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Most groups include between 7 and 10 members. We cap enrollment at 12 so everyone has an opportunity to participate.
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This is one of the most common questions I hear.
There isn't a test you have to pass or a certain level of illness you have to reach before you're "allowed" to ask for support.
Some members have lived with chronic illness since childhood. Others are newly diagnosed. Some have visible disabilities while others have conditions that people can't see.
If your health has changed the way you move through the world and you're looking for people who understand, this group may be a good fit.
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The group is a support group rather than a formal therapy group. The focus is on connection, conversation and learning from one another's lived experiences. While there may be moments of reflection or opportunities to consider new ways of approaching a challenge, the group is not structured around teaching therapeutic skills or completing exercises.
As the facilitator, Shannon helps guide the conversation, introduces topics that commonly arise when living with chronic illness and creates space for everyone to participate in a way that feels comfortable. Her background as a therapist naturally informs how she facilitates the group. She draws from approaches such as Motivational Interviewing, Acceptance and Commitment Therapy (ACT) and compassion-focused principles to encourage thoughtful discussion, support self-reflection and help members explore what matters most to them. These approaches shape the overall tone of the group rather than serving as a formal treatment model.
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Yes. Confidentiality is an important part of creating a group where people feel comfortable being honest and open.
Everyone who joins the group agrees to respect the privacy of other members and keep what is shared during sessions confidential. At the same time, you are never required to share personal information that you do not feel comfortable sharing, including your phone number, email address or social media accounts.
Some members choose to stay connected outside of the group, but exchanging contact information is always optional. Any sharing of contact information should be mutually agreed upon and coordinated with the facilitator so that everyone feels comfortable and respected.
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Many people living with chronic illness are already used to receiving advice they didn't ask for. Whether it comes from loved ones, strangers or people trying to be helpful, it can sometimes feel exhausting to constantly explain yourself or hear suggestions about what you "should" try.
This group is different. The goal is not to fix one another's problems or find the perfect solution. This is a space for sharing experiences, feeling understood and connecting with people who have lived through similar challenges.
Participants are encouraged to avoid giving advice unless someone specifically asks for it. Often, the most meaningful support is simply being heard and knowing that someone else understands.
Everyone's experience with chronic illness is different. A strategy that works well for one person may not fit someone else's life, body or circumstances. All members are encouraged to approach one another with curiosity, respect and compassion.
The group is built around mutual support and shared experience. Everyone is expected to help create an environment where people of all backgrounds and identities feel welcome and respected.
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No.
You're always welcome to listen until you feel comfortable. There is never any pressure to speak or share more than you're ready to.
Many members find that, as they get to know the group, they naturally begin sharing more about their experiences. Sharing at your own pace can deepen the benefits of the group, but listening, reflecting and simply being present are meaningful ways to participate too.
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Yes. Everyone deserves to be treated with respect and welcomed as they are. This group is LGBTQ+ affirming and committed to creating an inclusive environment.
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Living with chronic illness means life doesn't always go according to plan.
If you're unable to attend because of a flare, a medical appointment or another health-related reason, that's completely understandable. We encourage members to attend as consistently as they can because the group builds trust and connection over time, but we also recognize that health is unpredictable.
You don't have to be feeling your best to participate. Some weeks you may have plenty to say. Other weeks you may prefer to listen. You're welcome to turn your camera off for a few minutes, change positions, lie down, use mobility aids or make other adjustments that help you participate comfortably. If there are accommodations that would make it easier for you to attend, please let us know. We'll do our best to support your needs.
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Absolutely. Many people join this group because chronic illness has left them feeling isolated. Some are hoping to find others who truly understand what they're going through and would love to expand their circle with people who simply get it.
While building friendships isn't the goal of the group, it often happens naturally. Many members choose to exchange contact information near the end of the eight weeks and some continue talking, meeting up or supporting one another long after the group has ended.
Whether you stay connected outside of group is entirely your choice. There is never any expectation or pressure to share your contact information or continue relationships beyond the group.