LGBTQIA+

Going through cancer treatment is a big deal, both physically and emotionally. While you are dealing with a lot, you have the right to feel seen, heard, and treated with respect for who you are. Your identity is important. Healthcare should address the whole you, not just your diagnosis, and you have the right to feel safe in every single interaction. Young LGBTQIA+ people describe how cancer care can sometimes be based on assumptions, such as that everyone is cisgender, heterosexual, or fits into traditional gender roles and relationships. You may recognize yourself in this, or you may not. Regardless, it is important to know: it is never your responsibility to adapt to healthcare, but the other way around.

You choose how much you want to share about your gender identity, sexuality, or relationships. You should not have to explain your identity or what LGBTQIA+ means to be treated with respect. If you want to and have the energy to talk about it, do so. But it is never your responsibility to educate; the responsibility to have that knowledge lies with healthcare. At the same time, we know that many people appreciate it when healthcare staff are open, responsive, and want to understand. You have a right to that.

Sometimes conversations about the body, fertility, or the future may arise that do not truly reflect your reality. In those cases, it is completely okay to speak up. You have the right to receive information and support that feels relevant to you. It is important that you know you are not alone. There are others who have been in similar situations, and support is available both within and outside of healthcare. And if something feels wrong or does not go as it should, there are ways to take further action.

I often brought my girlfriend with me to the hospital and to medical appointments when I was ill. Most people treated us well, but on a few occasions staff asked if she was my friend or sister, and even if she was my mother… It would be so much better if staff asked who my loved one is without drawing their own conclusions.

When I was hospitalized for several weeks, I had a picture of us kissing displayed in the room. That way, the staff could see it and did not have to ask if I had a man or boyfriend.

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Ung Cancer is for young adults who are or have been affected by cancer, and for those who are close to someone who has, had, or died from cancer. Our thousands of members are between 16 and 35 years old, and membership is free.

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just found out

When everything becomes a blur after the word cancer. About the emotions, the crisis, and the questions you want to ask the doctor.

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the practical

Sickness benefits, compensation and insurance. Whether you are working, studying or unemployed.

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information

Reliable sources and source criticism, and how to find the right information on 1177, in your medical records, and in your care plan.

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your rights

What you are always entitled to in healthcare, from diagnosis to aftercare, and where to turn if something goes wrong.

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the body

About hair loss, scars and a body that feels new, and feeling whole in your own way.

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sexuality

About desire, closeness and intimacy during and after treatment, and that there is no right or wrong.

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fertility

About the possibility of having biological children, and why it is important to ask the question early.

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lgbtqia+

About the right to be seen and treated as you are. You choose what to share; providing the knowledge is the healthcare system's responsibility.

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fear of relapse

The fear that the cancer will return is one of the most common reactions. You are not alone in feeling this way.

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the cancer backlash

About life afterward, when you are expected to be "well" but nothing feels the same. Finding the new normal.

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late complications

Problems that can arise long after the treatment, and that you do not have to put up with without help.

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chronic cancer

About chronic cancer and palliative care, and living with as much quality of life as possible.

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