Do I Have Cystic Fibrosis Quiz

In 10 minutes, get a clearer sense of breathing, digestion, growth, and family history patterns linked to cystic fibrosis. Fast 15 questions deliver a focused self-check and smart next-step guidance to discuss with a clinician.
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Questions1510 minutes
Hi! My name is Freudly, i am an AI therapist, I will give you an interpretation of the test after you complete it.
08:30
July 22, 2026
July 22, 2026
Material has been updated
200 views
15 completions
64 likes
Verified by Daniel Hall
Psychologist with 25 years of experience
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Scale Explorer

How the Scales are Structured

example score
11/15
CF-Relevant History and Testing Signals (CRHaTS)
Measures how strongly your reported family history, screening results, or past testing signals align with possible cystic fibrosis and warrant record clarification or review.
No history/testing signal
Clarify the record
Prompt follow-up indicated
0NaNNo history/testing signal1NaNClarify the record3NaNPrompt follow-up indicated
A score of 11 falls in the “Prompt follow-up indicated” range, suggesting your responses include multiple or strong CF-relevant history/testing signals that may merit review of records.
example score
13/15
Digestion, Growth, and Salt-Loss Patterns (DGaSLP)
This scale reflects self-reported digestion issues, growth or weight concerns, and episodes suggestive of salt loss that can be seen in cystic fibrosis and other conditions.
No items endorsed
Worth discussing
Prompt clinical follow-up
0NaNNo items endorsed1NaNWorth discussing3NaNPrompt clinical follow-up
A score of 13 falls in the "Prompt clinical follow-up" range, indicating you endorsed multiple digestion, growth/weight, or salt-loss patterns that may warrant timely clinical discussion but are not diagnostic on their own.
example score
3/15
Persistent Respiratory Patterns (PRP)
Measures how often and persistently you report respiratory patterns such as mucus, recurrent infections, wheeze, or breathing difficulty that can be relevant when considering cystic fibrosis-like symptoms.
No items endorsed
Worth noting
Prompt clinical follow-up
0NaNNo items endorsed1NaNWorth noting3NaNPrompt clinical follow-up
A score of 3 falls in the Prompt clinical follow-up range, indicating you endorsed multiple persistent respiratory items in this section.
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DATA-BASED USER COHORTS

Who Usually Takes This Test?

Adults with chronic symptoms
41%OF USERS
People with ongoing cough, frequent chest infections, wheezing, fatigue, or hard-to-explain digestive issues use it to gauge whether cystic fibrosis is worth asking a clinician about.
Parents of symptomatic children
35%OF USERS
Caregivers take it when a baby or child has poor weight gain, greasy stools, persistent congestion or pneumonia, salty-tasting skin, or dehydration episodes.
Family history or carrier risk
24%OF USERS
Those with relatives who have cystic fibrosis, known carrier results, or past newborn-screening questions use it to understand what signs might warrant formal testing.
BASED ON AGGREGATED, ANONYMIZED DATA FROM TENS OF THOUSANDS OF FREUDLY USERS.
Benchmarking

See How You Compare

Once you complete the test, your results are compared with real-world data from people in your country.
Below is a preview of how scores are typically distributed across each scale.
CF-Relevant History and Testing Signals (CHaTS)
Average
9.8
Normal range
7.512.1
min.
0
max.
15
Majority
This curve shows how scores are typically distributed.
Once you complete the test, your result will appear on the scale so you can see how you compare.
Digestion, Growth, and Salt-Loss Patterns (DGaSP)
Average
5.2
Normal range
3.17.4
min.
0
max.
15
Majority
This curve shows how scores are typically distributed.
Once you complete the test, your result will appear on the scale so you can see how you compare.
Persistent Respiratory Patterns (PRP)
Average
8.8
Normal range
6.111.6
min.
0
max.
15
Majority
This curve shows how scores are typically distributed.
Once you complete the test, your result will appear on the scale so you can see how you compare.
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CLEAR ANSWERS TO COMMON QUESTIONS

Frequently Asked Questions

What does this quiz measure?
It reviews common cystic fibrosis-related patterns, including ongoing breathing symptoms, digestive or growth concerns, salt-loss episodes, and relevant family or testing history. It is a self-check and cannot confirm or rule out the condition.
How should the score results be interpreted?
Score bands are informational and are not validated clinical cutoffs. Similar symptoms can occur with many other conditions, so results should not be used to self-diagnose.
What should be done if the results suggest elevated concern?
Discuss persistent or worsening symptoms with a qualified clinician. A clinician may consider sweat chloride testing and/or genetic testing based on the full clinical picture.
When is urgent medical care needed?
Seek urgent help for severe breathing difficulty, blue or gray lips, confusion, fainting, or intense abdominal pain with vomiting or swelling. These signs require immediate evaluation regardless of quiz results.
How long does it take and how should items be answered?
Completion typically takes about 10 minutes for 15 questions. Answer based on typical patterns over time unless an item specifies a different timeframe.
WHAT THE TEST MEASURES
About This Assessment

Do I Have Cystic Fibrosis Quiz - Symptoms and Signs

This 15-question cystic fibrosis self-check helps you reflect on persistent breathing symptoms, digestion or growth concerns, salt-loss episodes, and relevant family or testing history. It cannot diagnose or rule out cystic fibrosis, and its score bands are not validated clinical cutoffs. Similar signs can have many causes. Discuss ongoing concerns with a qualified clinician, who may consider sweat chloride or genetic testing. Seek urgent help for severe breathing difficulty, blue or gray lips, confusion, fainting, or intense abdominal pain with vomiting or swelling.

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