The short answer
There is a real fertility problem, but not the simple one the headlines imply.
Canada is having fewer children than it did even a decade ago. The total fertility rate, which estimates the average number of children a woman would have over her lifetime if current birth patterns continued, fell from 1.58 in 2014 to a record low of 1.25 in 2024. That is a decline of approximately 21% in ten years and places Canada well below the population replacement level of approximately 2.1 children per woman. Canadians are also having children later. The average age at childbirth rose from 26.7 in 1976 to 31.8 in 2024.1 Looking toward 2050, Statistics Canada's current projection scenarios keep fertility below replacement, ranging from 1.09 to 1.55 children per woman, with a medium assumption of 1.32.2
A population's birth rate reflects when people start families, how many children they want, whether they can afford or support them, partnership patterns, access to care, pregnancy loss, and biological capacity.3 Clinical infertility has a different definition: failure to achieve pregnancy after 12 months of regular unprotected intercourse, with earlier evaluation appropriate in several circumstances.4, 7
The most defensible conclusion is more nuanced. People are trying later, when age-related reproductive decline matters more. Common conditions such as PCOS and endometriosis remain underdiagnosed. Metabolic health and some environmental exposures can affect reproduction. Male factors contribute in a substantial share of cases and are too often assessed late. At the same time, evidence is not strong enough to label every low birth rate, hormone change, or chemical exposure as proof of a biological fertility collapse.
We have strong evidence for reproductive aging, the fertility effects of specific medical conditions, and the harm of tobacco and exogenous testosterone. We have concerning population signals for sperm counts and environmental exposures, but uncertainty about cause, individual risk, and the degree to which they explain Canada's birth-rate decline.
Age affects both partners
The biology of delay is real, but it is not symmetrical.
Female age remains the single most important predictor of fecundity. The number of available oocytes falls over time, and age-related changes increase the proportion of eggs with chromosomal errors. This lowers the monthly chance of conception and increases miscarriage risk. The decline is gradual, not a cliff on a birthday, and varies between people. Still, postponing an attempt can narrow both the biological window and the range of treatment options.7, 8
Men also have a biological clock, although there is no menopause-like endpoint and no universally accepted age cutoff. With advancing paternal age, semen volume, motility, and morphology can decline, while sperm DNA fragmentation and new germline mutations tend to rise. Some studies associate older paternal age with lower assisted reproduction success and certain pregnancy or offspring outcomes.9, 10
Risk communication matters. Most children of older fathers are healthy, and the absolute risk of any one rare outcome remains low. Paternal age should be part of counseling and shared planning, not a source of blame or a claim that sperm becomes suddenly unsafe at 40.
Beyond ovarian aging
PCOS, endometriosis, and metabolic health can compound the effect of time.
Polycystic ovary syndrome
PCOS affects an estimated 10% to 13% of reproductive-aged women worldwide, and the WHO estimates that up to 70% may be unaware they have it. It is a hormonal and metabolic condition commonly associated with irregular or absent ovulation, higher androgen levels, and insulin resistance. Despite the name, ovarian cysts are not required for diagnosis.15
PCOS is a leading cause of anovulatory infertility, but it is also one of the more treatable causes. Lifestyle support, management of metabolic risks, and ovulation-induction treatment can be effective. More diagnoses do not necessarily prove that the underlying disease has suddenly become more common. Better recognition and broader diagnostic frameworks also change measured prevalence.
Endometriosis
Endometriosis is a chronic inflammatory disease in which tissue similar to the uterine lining is found outside the uterus. It affects roughly one in ten women and gender-diverse people, yet Canadian diagnosis can take at least five years. It may impair fertility through inflammation, adhesions, altered pelvic anatomy, tubal effects, or ovarian involvement.16
Not everyone with endometriosis is infertile, and symptom severity does not reliably predict fertility impact. Persistent pelvic pain, painful periods, pain with sex, bowel or bladder symptoms that track with the cycle, or a relevant family history justify earlier assessment. Waiting for 12 months of trying is not required when disease is suspected.
Metabolic health and body size
Measured Canadian data show that 68% of adults aged 18 to 79 had a BMI in the overweight or obesity range in 2022 to 2024, compared with 60% in 2016 to 2019.17 Higher BMI is associated, on average, with more ovulatory dysfunction, pregnancy complications, and lower response or success in some fertility treatments. Adipose tissue participates in hormone signaling and inflammation, and insulin resistance can amplify PCOS.18
Association is not destiny. People in larger bodies conceive naturally and through treatment. A target weight should not become an endless barrier to assessment, especially when age is also reducing fertility. Preconception care should be respectful and focus on blood pressure, glycemic health, nutrition, movement, sleep, medications, pregnancy safety, and the person's priorities. Weight-loss interventions before IVF have not consistently improved live-birth rates, so delay requires an individualized risk-benefit discussion.18
Other female factors also matter, including tubal damage after infection, fibroids or uterine abnormalities, diminished ovarian reserve, thyroid or prolactin disorders, prior ovarian surgery, and gonadotoxic cancer treatment. A good assessment follows the history rather than assuming every person needs the same panel.
Male fertility is half of the first assessment
Sperm health, sexual function, and testosterone require careful interpretation.
A widely discussed meta-analysis estimated a substantial decline in average sperm concentration and total sperm count among unselected men from 1973 to 2018.13 This is a concerning population signal. It is not proof that every man's fertility has halved, that one exposure caused the trend, or that sperm count alone determines pregnancy. A newer study of confirmed fertile men in the United States did not find a clinically meaningful decline over its study period.14 Differences in populations, collection methods, geography, and study design remain important.
A semen analysis is usually the highest-value first test for a male partner. Results should be interpreted as a pattern, and an abnormal result is often repeated because semen parameters vary. Sperm DNA fragmentation testing can be useful in selected situations, but professional guidelines do not recommend it as routine initial testing. The result does not identify one cause or guarantee that a particular treatment will improve live birth.10
Testosterone can improve a blood level while suppressing sperm production.
External testosterone and anabolic steroids suppress the brain signals, LH and FSH, that support sperm production. Severe oligospermia or azoospermia can result. Testosterone monotherapy should not be prescribed to someone who wants current or future fertility. Anyone already taking it should speak with the prescriber or a reproductive urologist rather than stopping abruptly.11, 12
It is also too simplistic to state that testosterone falls by exactly 1% each year and therefore sperm count falls with it. Hormone trajectories vary with sleep, body composition, chronic illness, medications, and other factors. Low libido, erectile or ejaculatory difficulty can lengthen time to conception and deserve clinical attention, but a serum testosterone value is not a substitute for semen analysis.
Male evaluation should happen at the same time as female evaluation. Sequential care can lose months, reinforce stigma, and miss an immediately actionable factor.
Concern without catastrophizing
Environmental exposures matter. “Detoxing” is not the answer.
Research links some pesticides, solvents, heavy metals, air pollutants, phthalates, bisphenols, and persistent organic pollutants with reproductive or developmental outcomes. Plausible mechanisms include endocrine disruption, oxidative stress, altered cell signaling, and epigenetic change. The evidence is strongest for some occupational or high-dose exposures. For everyday mixtures at typical levels, measuring an individual's exact fertility effect is difficult.10, 19
Animal and experimental studies raise legitimate questions about epigenetic effects across generations. They do not justify telling an individual that ordinary exposure has permanently “rewritten” their sperm or eggs, or that a commercial cleanse can reverse it. “Body burden” describes accumulated chemical exposure; it is not a clinical diagnosis.
Do not heat food in plastic. Use glass or stainless steel when practical.
Wash produce and follow local advice about fish, lead, water, or air hazards.
Choose fragrance-free personal and household products when feasible.
Use protective equipment and occupational health support around solvents, pesticides, metals, radiation, or high heat.
These are reasonable exposure-reduction steps, not a promise of improved fertility. Individual action has limits. Product regulation, safer workplaces, pollution control, and better biomonitoring are public-health responsibilities.
The highest-value window
Why preconception planning matters
Preconception care is not a luxury wellness phase. It is the time to find risks that are easier to address before pregnancy, identify when trying without assessment may waste valuable time, and make pregnancy safer if conception occurs quickly.
A visit about three months before trying is practical when possible. It allows time to begin folic acid, review medications and vaccines, improve chronic disease control, address substance use, and evaluate symptoms.5, 6 It also spans much of the sperm-development cycle. Three months is a planning window, not a rule to delay conception or fertility referral.
Age, irregular cycles, pelvic symptoms, testicular history, sexual dysfunction, or prior treatment may justify earlier investigation.
Medication, supplement, infection, immunity, occupational, and substance-use review can identify changes best made before pregnancy.
Blood pressure, diabetes, thyroid disease, anemia, mental health, nutrition, and other conditions can be optimized in context.
Earlier information creates time for natural attempts, treatment, referral, fertility preservation discussion, or a revised family-building plan.
Planning cannot guarantee pregnancy, stop ovarian aging, measure “egg quality,” or cleanse reproductive cells. Its value is better decisions, safer preparation, and earlier access to appropriate care.
A targeted, two-partner approach
What a practical preconception plan can include
- 1Clarify goals and timing.
Discuss desired family size, when you hope to start, age-related considerations, contraception, and any reason your timeline may need to change.
- 2Review both reproductive histories.
Include cycles and ovulation, pelvic symptoms, prior pregnancies or losses, infections, surgery, cancer treatment, testicular injury, erections and ejaculation, and family history.
- 3Review every medication and supplement.
Do not stop prescribed treatment independently. Flag testosterone or anabolic steroids, medications unsafe in pregnancy, and supplements with uncertain dose or purity.
- 4Optimize health without perfectionism.
Address smoking and vaping, cannabis, alcohol, sleep, movement, nutrition, dental care, chronic conditions, mental health, vaccination, and relevant occupational exposure.
- 5Start folic acid.
For most people who could become pregnant, Health Canada recommends a daily multivitamin containing 0.4 mg of folic acid, ideally beginning at least three months before pregnancy. Higher doses should be clinician-directed.6
- 6Order tests that answer a clinical question.
This may include targeted general health or hormonal tests, pelvic imaging, tubal assessment, or semen analysis. It should not automatically mean a large fertility panel.
- 7Set a clear review point.
Know when to return, what symptoms trigger earlier care, how results will be interpreted, and when a fertility, gynecology, or reproductive urology referral is appropriate.
AMH and other ovarian reserve tests do not reliably predict short-term natural conception in people without infertility. Routine sperm DNA fragmentation testing, broad hormone panels, and unvalidated “toxicity” testing can create cost and anxiety without changing care. Testing should be selected because a result can inform a decision.7, 10
Do not wait by default
When to seek a fertility evaluation
Seek care earlier at any age for absent or very irregular periods, suspected endometriosis or tubal disease, known uterine or ovarian disease, recurrent pregnancy loss, prior chemotherapy or pelvic radiation, a history that could affect the testes, known abnormal semen results, sexual dysfunction, or another condition known to affect fertility.7, 10
Evaluation should begin with both partners when applicable. It should assess ovulation, reproductive anatomy or tubal patency when indicated, and semen. The purpose is not to run every available test. It is to locate the highest-value next decision.
Future projections and response
Low birth rates are likely to persist. Biological infertility is harder to forecast.
Statistics Canada's current scenarios all keep fertility below replacement through 2050.2 International modelling also projects that most countries will remain below replacement by mid-century.22 These projections matter for schools, labour markets, healthcare, migration, and aging populations.
They still cannot tell us how many Canadians will meet a medical infertility definition in 2035 or 2050. That would require current, repeated data on time to pregnancy, pregnancy loss, reproductive diagnoses, male factors, treatment access, and who is trying to conceive. Treating a demographic projection as a biological forecast overstates the evidence.
A credible response therefore works at two levels:
- For individuals: earlier fertility education, inclusive preconception care, timely diagnosis of PCOS and endometriosis, parallel male assessment, STI prevention and treatment, tobacco cessation, evidence-based exposure reduction, and prompt referral when age or history warrants it.
- For health systems: better national surveillance, shorter diagnostic delays, fertility preservation counseling before gonadotoxic treatment, affordable and geographically equitable care, and reproductive health research that includes men.
- For society: childcare, housing, income security, parental leave, flexible work, and environmental and occupational protections. Biology and social conditions are not competing explanations. They interact.
The bottom line
Preconception planning turns uncertainty into an earlier, more informed decision.
Canada's record-low birth rate deserves attention, but alarm is not a clinical strategy. The useful response is to respect reproductive aging, investigate symptoms sooner, include male fertility from the start, reduce well-supported risks, and avoid overpromising what a test or “detox” can reveal. Good planning protects time without pretending biology is fully controllable.
Sources and review notes
Evidence used in this article
This review prioritizes Statistics Canada, Canadian public-health guidance, the World Health Organization, and professional society guidelines. Evidence was reviewed August 23, 2026. Clinical recommendations change, and individual care depends on history and jurisdiction.
- Statistics Canada: Fertility and baby names, 2024
- Statistics Canada: Population projections, fertility assumptions, 2025 to 2075
- Statistics Canada: Fertility intentions and childlessness, 2024
- WHO: Infertility fact sheet
- Public Health Agency of Canada: Preconception care
- Health Canada: Folic acid before and during pregnancy
- ASRM: Fertility evaluation of infertile women
- ASRM: Optimizing natural fertility
- ASRM: Advancing paternal and maternal age
- AUA and ASRM: Male infertility guideline, evaluation
- AUA and ASRM: Male infertility guideline, treatment
- Endocrine Society: Testosterone therapy guideline
- Levine and colleagues: Temporal trends in sperm count
- Boulet and colleagues: Sperm counts in confirmed fertile US men
- WHO: Polycystic ovary syndrome fact sheet
- SOGC: Endometriosis
- Statistics Canada: Measured overweight and obesity, 2022 to 2024
- ASRM: Obesity and reproduction
- ACOG: Reducing prenatal exposure to toxic environmental agents
- WHO: First global guideline on infertility
- Public Health Agency of Canada: Infertility guidance and Canadian prevalence estimates
- The Lancet: Global fertility scenarios to 2100
A focused next step
Bring the clinical question into a coordinated plan.
Asali Health provides referral-based virtual fertility optimization consultations for women and men in Ontario and British Columbia.
