Welcome to A Body Rebels: A Chronic Illness Podcast!
Oct. 6, 2026

Chronic Illness, Depression, and Losing Friends After Diagnosis

Chronic Illness, Depression, and Losing Friends After Diagnosis

In this episode of A Body Re-bells: A Chronic Illness Podcast, I respond to a listener living with pulmonary sarcoidosis, depression, family estrangement, and the loss of friendships after diagnosis. I talk about what friendship looks like when illness stops being temporary, why suicidal thoughts deserve immediate professional support, and what happened when one of my own friendships ended after I revealed how sick I was. I also share what twenty years with sarcoidosis taught me about accepting when some people are unable to handle serious illness.

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

Contact A Body Rebels

More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research

SPEAKER_00

The email began with a polite greeting. I read on and reached a sentence where I stopped. JJ had written about pulmonary sarcoidosis, depression, friends disappearing, family estrangement, and thoughts of ending their life. I went back and read the sentence again. Welcome to a body rebels. I'm Tate. This podcast shares my personal experiences and is not medical advice. Please speak with your own provider before making medical decisions. The voice you're hearing is AI because illness makes speaking difficult, but the writing, memories, opinions, and experiences are mine. Please note that this episode deals with thoughts of self-harm. I'm responding to what happens when chronic illness changes your life, and some of the people you expected to stay quietly leave. JJ was diagnosed with pulmonary sarcoidosis last year. They're taking methotrexate, and they wrote the medication seems to be helping. Then the email moved away from treatment and into something harder to measure. JJ lives with depression. Before sarcoidosis, they had a wide circle of friends. Those friends seemed able to tolerate the depression more than support JJ through the worst periods. People checked in, pulled away, then returned after JJ seemed normal again. JJ put normal in quotation marks. I understood why. When I'm sick, there are days when looking familiar to other people takes work. A conversation goes better if I sound steady. Someone relaxes when I say, I'm okay. The harder answer takes longer, and the person asking doesn't always know what to do with the truth. For JJ, sarcoidosis changed the equation again. Friends pulled farther away. Some ghosted them. JJ is estranged from family, so there wasn't another dependable circle waiting behind the first one. Then came the sentence about suicide. I don't want to hurry past those words simply to get back to a discussion about friendship. I wrote back to JJ and told them to get help immediately. I wanted to be clear because thoughts of suicide deserve an immediate response, especially when someone feels unsafe or fears they might act on them. In the United States and its territories, call or text 988 for the Suicide and Crisis Lifeline. The service is free, confidential, and available around the clock. In England, call NHS 111 and select the mental health option for urgent mental health support. Samaritans also answers free, day or night at 116-123. If you're in immediate danger, contact local emergency services or go to the nearest emergency department. Say the words plainly. A podcast offers company. A crisis counselor, emergency team, or mental health professional offers something different. They're there for the moment when staying safe needs more than listening to a familiar voice through headphones. I'm glad JJ wrote to me. I'm glad this show felt safe enough for a letter like theirs. I also want the next reach to go farther than my inbox. I'm always willing to hear from someone who needs a listening ear. If you want to write to me or leave a voicemail, you can contact me through the podcast website at abodyrebels.com. I'm not a medical professional and I don't have answers for somebody else's health, but I'm here to listen. I read and answer every message I receive. I have lived with sarcoidosis for 20 years. Those years have included fear, anger, exhaustion, appointments, uncertainty, and plenty of difficult days. I'm also a loner. I'm comfortable with my own company. I don't need people around me in order to feel secure, occupied, or complete. Being alone and being lonely are two different things for me. What I do need is proper medical help when my health requires it. I need physicians who know my history. I need treatment. I need testing when something changes. I need people with the training to deal with medical problems I cannot deal with myself. That is different from needing a circle of people around me all the time. So when I talk about losing friends, I'm not talking about being unable to function without them. I'm talking about what happens when someone you considered a friend learns the reality of your illness and decides, for whatever reason, to disappear. For JJ, losing friends after diagnosis hurts for a specific reason. Ghosting leaves no clean ending. Nobody sits down and says, your illness scares me, or I don't know how to help. Or I only knew how to be close to you when your needs were easier for me. The messages slow down, replies get shorter, plans disappear. Eventually, silence becomes the answer. I know something about that kind of silence. I had a friend I knew back in the 90s. We lost touch for a while, then reconnected during the early years of my illness. At the time, this friend didn't know the extent of what was happening with my health. She came to my house for a dinner party. During the evening, I mentioned offhandedly that I was dealing with an autoimmune disease. I didn't give much detail. She happened to work with a naturopath, so I asked whether he saw people with autoimmune diseases. That led to more questions about my health. I'm careful about telling people everything. There's a reason for that. Once I start listing everything wrong with me, some people begin looking at me differently. Before the conversation, they see the person they've always known. Afterward, I sometimes see the shift. Now they're looking at someone who is seriously ill. I don't enjoy living under that look. So I usually keep a lot to myself. Against my better judgment, I told this friend everything. I explained the disease and the extent of my health problems. She seemed fine with what I told her. She said she would call me the next morning and arrange an appointment with the naturopath. I later learned the naturopath was her boyfriend. The next morning, she called. She didn't call to arrange the appointment. She said, Tate, I don't think seeing Dr. X is a good idea. I think you should see another doctor. I didn't ask why. I said, okay. Thanks. Then I hung up. I never heard from her again. There was no argument, no explanation, no goodbye. I never knew for certain what happened between the dinner party and the phone call the next morning. What I heard in her message, and especially in the silence afterward, was something much simpler. Tate, I can't handle your disease. I can't cope with seeing you now that I know how sick you are. Maybe those weren't her thoughts. I have no way of knowing. But that was the message her disappearance left with me. And I accepted the friendship was over. I didn't chase her. I didn't demand an explanation. I didn't try to convince her I was still the same person she had known before she heard my medical history. I knew who I was. My diagnoses hadn't changed me overnight. Her knowledge of them had changed the way our relationship worked. That experience stayed with me because it confirmed something I had already begun noticing. Sometimes people handle the version of me who looks okay. They struggle with the full medical reality sitting underneath. Then the person left behind starts examining every conversation. Did I talk about my health too much? Did I ask for too much? Was I too depressed? Did I become exhausting? Those questions make sense after rejection. They still don't provide reliable answers. A friend's withdrawal tells me what the friend is willing or able to bring into a relationship. A friend's withdrawal doesn't measure the value of the person who got sick. Some people manage a crisis better when the crisis has a clear finish line. Surgery happens, flowers arrive, recovery begins, everyone moves forward. Sarcoidosis doesn't follow somebody else's preferred schedule. Neither does depression. Treatment separately at fatigue returns. A medication helps one part of life while adding new problems somewhere else. A bad week arrives after a better month. Friends who need a clean ending often struggle with a story still in progress. Understanding why someone pulls away doesn't erase the harm. There is a difference between a friend who is awkward around illness and a friend who repeatedly disappears when life gets hard. If someone still seems willing but lost, one clear request might help. Send me a message on Sunday. Please check in even if I don't sound cheerful. Stay on the phone with me for a few minutes. Specific requests remove some of the guessing. A willing friend gets a place to start. If the same person keeps vanishing after a clear request, the pattern speaks for itself. Illness also changed what I expect from friendship. I don't need every person in my life to understand sarcoidosis. I do value honesty. If somebody feels overwhelmed by my health, I'd rather know. I also don't spend limited energy persuading someone to stay in my life. My experience with a friend from the 90s taught me that. She disappeared. I accepted it. I moved on. For someone such as JJ, though, friendship carries another weight because depression and isolation are already part of the picture. Losing people during a mental health crisis creates a different level of risk. A sarcoidosis support group is one place to look for connection. Online groups count. In-person groups count. Shared diagnosis doesn't guarantee friendship, but there's often less explaining to do. Another person with chronic illness understands why treatment helping the disease still leaves you exhausted. Another person understands the strange mix of gratitude and anger around medication. Another person knows why, how are you? sometimes has a short answer for public use and a longer answer reserved for people who mean the question. I think of those connections as chronic illness kinship. The phrase doesn't mean everyone with sarcoidosis becomes family. I've met enough human beings to know better. The phrase means less translation before a conversation begins. Professional mental health care belongs in JJ's situation too, especially after a sentence about ending life. I'd want JJ to tell a qualified mental health professional exactly what they told me. Not I've been feeling a little low. The actual sentence. I sometimes feel like ending my life. Direct words give the other person a clearer picture of the danger. For someone experiencing suicidal thoughts, preparing a crisis plan before another severe low point also makes sense. A clinician or crisis professional could help put one together. The plan might identify who to contact, where to go, which professional to call, and what steps will make the environment safer if the risk becomes immediate. That advice is for someone facing suicidal thoughts. It isn't a description of my own mental health. I don't have depression, and I don't experience suicidal thoughts. JJ's situation is different from mine, which is exactly why professional mental health support matters here. When depression, lost friendships, family estrangement, illness, and fear arrive together, the future can start looking like one enormous problem. JJ doesn't need to solve an entire life during one terrible hour. The immediate job is staying safe. After the immediate danger passes, the next step might be treatment, a conversation with a therapist, a support group, a meal, some rest, or contacting one person who understands what is happening. In my original response to JJ, I used a line I no longer like. I told them they had survived 100% of their hardest days. I understand the intention behind the phrase. I don't want to use the phrase as reassurance here. A person who survived every earlier crisis still needs immediate help during a dangerous crisis today. Past survival doesn't remove present risk. What matters to me in JJ's letter is the act of reaching outward, JJ wrote. Old friendships aren't the complete list of relationships available for the rest of a life. New support might look different from what JJ hoped for. A therapist won't replace a missing friend. A support group won't repair family estrangement. A crisis counselor won't erase the grief of being ghosted. Each relationship serves a different purpose. What matters here is whether JJ has appropriate support for the dangerous hours and meaningful connection for the ordinary ones. I also want to say something to the friend on the receiving end of a sentence about suicide. Don't hunt for a brilliant response. Listen. Take the words seriously. Ask about immediate safety. Help the person reach trained support or emergency care. Stay nearby when doing so is safe. You don't need to solve depression. You don't need to explain why life is worth living. You don't need a speech. You need to avoid disappearing because the conversation became frightening. Sometimes friendship looks like sitting beside someone while the next call gets made. I'm Tate. Thanks for sharing this time with me. Until next time, take care of yourself. Keep breathing and remember sarcoidosis is only rare until you're the one living with it.