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Cystic fibrosis patients dating other cystic fibrosis patients

It is simply a decision that the individual may have made even prior to being with you.If it is a deal-breaker, then you will be able to move on to find someone who has not identified this concept as such and ultimately will accept everything about you. No need to blurt out information related to your diagnosis.

Telling people you have CF is a personal choice, and you actually do not have to disclose it to every person you meet.It will impact factors such as honesty, openness, ability to welcome supportive assistance, participation in healthy boundaries and assertive communication, as well as engaging in vulnerability and trust.Tips on how to talk to your new partner about CF: Practice what to say.You can follow-up with something like, “I don’t see this as something that defines me, and if I need help, please leave it to me to ask.” Know when to give your partner space.Even if you deliver a perfect speech about your condition, it is still possible to experience that ‘awkward moment’ following your disclosure.Each person’s decision as to when and how to include their partner is quite individualized.There is no specific timeline or rule on including your partner into your medical regimen; however I must emphasize the benefit (to you, as well as the relationship) of welcoming that person into your support system.If things were going well up until the time you told them, keep in mind that they rejected your health condition, not you.At the end of the day, it means that they were not the one.If this happens, you can respond with, “I can tell by your expression that this is a lot to digest and I completely understand, and I’ll give you time and space to do that.” You can give physical space, but maintain contact.Consider the etiquette of giving at least 24 hours, then reaching out for a response.

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  1. Shortly before my medical training, there were a lot of “CF camps” out there where children with CF could get together, bond, share their experiences with each other, learn about their disease, etc. They were great for the young patients' morale. But there was a big downside, and it's the reason why CF.

  2. Although cystic fibrosis is a rare disease, in some schools there may be more than one person with CF present. Germs are a major concern for. When there is more than one person with CF in your school, it is essential that they be kept a minimum of 6 feet 2 meters apart from each other. Germs can spread as far as 6 feet.

  3. Posted by Summer Katz, M. A. NCC, LMHC Patient Advocate. Dating and intimacy can be both desired as well as confusing, or even become quite complicated to navigate; certainly when trying to determine how or when to handle discussing cystic fibrosis with your new partner. Telling people you have CF is a personal.

  4. Apr 1, 2015. Cystic fibrosis patients shouldn't be near each other because they can share infections that could cripple their already fragile lungs. Dr. Michael Anstead at the University of Kentucky, Katie's pulmonologist since she was a little girl, had lectured her many times that face-to-face meetings with other CF.

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