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Breathing Room has lots in store for the year. If you would like to share your personal stories, news items or poetry with us, please contact: us at: info at thebreathingroom.org.

Stories, Poems and opinions of participants are their own, and not necessarily those of the Breathing Room organization.


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Breathing Room
facilitates candid and open communication between adults with Cystic Fibrosis, supports the development of a community of adults with CF and provides education and insight for families, caregivers, and medical professionals who impact our lives.

A Sense of Service Continued

Melissa

My sense of service is because of three reasons.

First, I never had anyone to connect too about my CF. I felt totally alone my whole life. I didn't realize how much my 'loneliness' had to do with my CF, and not having anyone to connect to. I would love to have the honor to help someone, even if it is only one person, not feel alone.

Second, when I was waiting for my transplant, I had no idea in the world what to expect. I was afraid to ask questions, afraid of what I would find out. The doctors were very vague about what to expect. I met a wonderful woman named Tina Williams, that told me exactly what to expect. She let me ask every question I had, down to what should I do with my hair. She was amazing and I don't think I would have been able to handle the wait without her. I owe her more than she knows.

Lastly, I do it for my donors. They went into surgery and gave me part of their body just to help me. They did not have to, and could have easily not have offered, but they did and I am still alive almost four years later. I do this to give back in the only way I know how. I want them to be proud of me, and this is one way I know they will be.

Melissa Thompson (Reta)


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