Bart

Bart had a malignant tumour removed after a Bowel Cancer Screening test. He has since had further surgery to reduce the chance of recurrence. He was invited to take part in the 100,000 Genomes Project while waiting for an appointment at the hospital. He did so because he wants to encourage others to take part in bowel cancer screening, as well as to support medical genetic research.

Bart took part in the Bowel Cancer Screening Programme and his test showed abnormal readings. A colonoscopy procedure was carried out to remove two polyps, one of which was found to be malignant. He had surgery to remove a small part of the intestine where the malignant polyp had grown to increase the chances of a successful outcome.

During a hospital appointment, Bart was approached by a health professional who invited him casually to take part in the 100,000 Genomes Project. He was happy to be involved because he wants to encourage others to take part in the Bowel Cancer Screening Programme. Another main motivation to take part in the project was to support medical research with the development of new treatments and early interventions. He hopes that this could help to safeguard the health of his children, grandchildren and society in general. Bart feels very positive and grateful for the medical care he has received.

Looking back, Bart found the information given about the project too detailed and complex. As an education professional he doesn’t think that the style or language used in the patient information pack is accessible to everyone. Nevertheless, he understands that medical research needs to comply with regulations to protect personal information and data. He says he would have signed the consent form anyway because it is genuine research that he feels deserves support.

Overall, Bart found the experience of participating in the 100,000 Genomes Project a positive one. He felt well informed and didn’t find donating of tissue samples problematic. He says that the consent process was done in a friendly, supportive and sympathetic manner. He feels that the health professional that took consent from him understood his situation, and was aware that he had just been diagnosed with cancer.

Bart urges everybody in his position to sign up and take part in the project because, as he puts it, the more people that get involved the more information, the more data, the more experimentation that can take place will lead to the breakthrough that we all so desperately need.

Bart found the part about data protection quite technical but wasn’t surprised and thought it was appropriate given the subject matter.

Age at interview 61

Gender Male

Age at diagnosis 60

Bart’s son studies biology and chemistry so he understands the importance of research. He wanted to participate to help others in future.

Age at interview 61

Gender Male

Age at diagnosis 60

Bart believes everyone should sign up to be involved in medical research to develop understanding of how our genes contribute to cancer.

Age at interview 61

Gender Male

Age at diagnosis 60

Bart wishes he understood the project a bit more technically and hopes that there will be much-needed breakthroughs in the future on cancer.

Age at interview 61

Gender Male

Age at diagnosis 60

Bart can’t remember who approached him to take part because he was more concerned about what the consultant was going to be saying to him.

Age at interview 61

Gender Male

Age at diagnosis 60

Although Bart hadn’t heard of the project, his son works in science and he knows about the importance of genetic research.

Age at interview 61

Gender Male

Age at diagnosis 60