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Kadeem M

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@kadeemm

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    Kadeem M replied to the topic "Does Educating Others About Your Disease Feel Like a Blessing or a Curse?" in the forum Adults​ ​With​ ​Cystic Fibrosis 3 years, 5 months ago

    Personally I feel that if I have to educate someone about Cystic Fibrosis, I have to give them a crash course. And where there are grey areas, they would ask questions in which results in me going deeper into a lecture syle of teaching. Personally, I find it a blessing in a sense where I am able to educate someone about a topic I know so well…[Read more]

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    Kadeem M replied to the topic Building trust in a healthcare setting in the forum Adults​ ​With​ ​Cystic Fibrosis 3 years, 6 months ago

    This is very well thought out and written.

    I found throughout my paediatric care (age 0-18), it was a lot easier to develop a sense of trust with my healthcare team regarding my overall health. Main factor being that since i was a minor, for majority of the years my parents would be making my medical decisions, and they never ever disagreed with…[Read more]

    • Profile picture of Bailey Vincent
      Bailey Vincent replied 3 years, 6 months ago

      I have heard a lot of people say this about adult health care versus pediatric. I think, sometimes, we feel less important as adults. Like physicians are less invested in our lives and the quality of them?

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    Kadeem M started the topic Post-Transplant. in the forum Adults​ ​With​ ​Cystic Fibrosis 3 years, 6 months ago

    My name is Kadeem, 23 years old and about to hit my 3 year post-transplant anniversary. It was just three years ago I had fallen ill do another contracted infection in which caused me serious chest pain, chest tightness, long strung-out coughing fits that would leave my heart racing and me gasping for air afterwards. I couldn’t speak a sentence w…[Read more]

    • Profile picture of Jenny Livingston
      Jenny Livingston replied 3 years, 6 months ago

      @kadeemm thank you for your vulnerability and willingness to share this post. Although our stories are very different, I can relate to some of the things you describe here. I, too, have lost so many friends to CF while I continue to do well. I’ve had the opportunity to try and benefit from new drugs, while so many people I know are unable to. It…[Read more]

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    Kadeem M became a registered member 3 years, 6 months ago

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    Kadeem M changed their profile picture 3 years, 6 months ago

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This site is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

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