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CELPIP Practice Reading: Reading for Viewpoints ID: #63259 Hard My Father's Heart and a New Mortgage

Read the following blog post from a website.

My father died of a heart problem at fifty-two, and last spring my cardiologist suggested a genetic test to see whether I carry the same risk. I still have not booked it. My partner and I are buying a house, the bank wants life insurance on the mortgage, and I keep wondering whether a positive result would follow me into every application. So I have kept a close eye on Parliament’s review of whether life insurers should ever be allowed to see predictive genetic results.

Anselma Rivard, whose law practice serves rare-disease clinics, argues that people like me are the reason for a firm ban. “Patients already skip tests their doctors recommend because they fear an insurance company will read their DNA like a warning label,” she told the review. In her view, a large pool of customers can absorb a few high-risk results without questioning everyone’s genes. Barnabas Thorsen, an actuary for a mutual insurer, argues the other side. He says hiding a known risk simply moves its cost onto other policyholders, and he points out that insurers already price family history, which in my case is no secret. He could live with required counselling and a waiting period before any result is shared, but not with a ban.

Ngozi Chukwu, head of a national ethics panel, argues for a narrower path. She says insurers could ask only about gene types that doctors already use to choose treatment, while results from home ancestry kits would stay out of every file. Any longer list, she adds, would need a review by outside ethics experts and an expiry date, so that Parliament must look at the rule again. Fabian Durocher, a genetic counsellor, notes a quieter problem: some of his patients now ask to pay for tests privately so the results never reach their medical chart. He wants the rules printed in plain words on every consent form, so people know the stakes before they give a sample.

I started this reading hoping for Rivard’s ban, and part of me still does. But Thorsen’s point stings, because my father’s history is already on every form I fill out. Chukwu’s short list feels like the honest middle, as long as the expiry date is real. For now, I have decided to stop waiting for Parliament. I booked the test for next month, and I will deal with the insurer once I know what my heart is doing.

Using the drop-down menu (▾), choose the best option according to the information given on the website.

This blog post is mainly about 1.
.

Who most clearly doubts that a ban would be fair to other customers? 2.
.

Fabian Durocher’s concern would most likely be supported by 3.
.

What outcome does Ngozi Chukwu’s condition call for? 4.
.

The blogger mentions buying a house mainly to 5.
.

The following is a comment by a visitor to the website page. Complete the comment by choosing the best option to fill in each blank.

My mother carries a gene linked to breast cancer, and she has kept that result inside the family for ten years. Anselma Rivard believes that 6.
. How I wish that were true for families like mine. The actuary names 7.
as terms he could live with, and I copied that line into my notes. Ngozi Chukwu would let insurers ask only about 8.
, and I can see the sense in drawing the line there. My brother works in a pharmacy, and he says customers ask him about genetic testing almost every single week now. Fabian Durocher wants the rules printed in 9.
, and I hope the review listens to him. I am sorry the blogger lost a father at 10.
, and I hope next month’s appointment brings good news.

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