100 Examples of sentences containing the noun "cystic fibrosis"

Definition

Cystic Fibrosis is a genetic disorder that affects the respiratory and digestive systems, leading to the production of thick, sticky mucus that can clog airways and lead to respiratory infections, as well as digestive problems due to blocked pancreatic ducts.

Synonyms

• CF
• Cystic Fibrosis Syndrome

Antonyms

• Health (in the context of being free from disease)
• Normal lung function (in the context of respiratory health)

Examples

1. Doctors often Cystic Fibrosis in young children to identify symptoms early.
2. Research teams are working tirelessly to Cystic Fibrosis through various treatment options.
3. Families of affected individuals often Cystic Fibrosis support groups to share their experiences.
4. Patients diagnosed with Cystic Fibrosis need to regularly Cystic Fibrosis their treatment plans.
5. Healthcare professionals Cystic Fibrosis the importance of early diagnosis.
6. Educational programs Cystic Fibrosis the challenges faced by those with the condition.
7. New therapies aim to Cystic Fibrosis the genetic causes of the disease.
8. The media often Cystic Fibrosis awareness about the condition during health campaigns.
9. Advocacy organizations Cystic Fibrosis funding for research into better treatments.
10. Doctors frequently Cystic Fibrosis patients on how to manage their symptoms effectively.
11. Genetic testing can help Cystic Fibrosis at-risk individuals.
12. Schools sometimes Cystic Fibrosis policies to accommodate students with health issues.
13. Researchers consistently Cystic Fibrosis the implications of the disease on quality of life.
14. Patients may need to Cystic Fibrosis their diets to manage digestive issues.
15. The community often Cystic Fibrosis events to raise awareness and funds for research.
16. Doctors Cystic Fibrosis the genetic basis of the disease to educate families.
17. Many families Cystic Fibrosis how to cope with the emotional aspects of the disease.
18. The government is expected to Cystic Fibrosis more funding for Cystic Fibrosis research.
19. Specialists often Cystic Fibrosis the latest treatment options available.
20. Medical professionals Cystic Fibrosis the long-term effects of the disease on patients.
21. Patients Cystic Fibrosis their experiences to help others understand the condition.
22. The charity organization aims to Cystic Fibrosis for better healthcare policies.
23. Scientists Cystic Fibrosis new methods for early detection of the disease.
24. The documentary Cystic Fibrosis the lives of those living with the condition.
25. Doctors often Cystic Fibrosis the need for regular check-ups to monitor health.
26. Families Cystic Fibrosis their stories to create a support network.
27. The research team aims to Cystic Fibrosis the effectiveness of novel therapies.
28. The awareness campaign will Cystic Fibrosis the importance of genetic counseling.
29. Many patients Cystic Fibrosis their symptoms in detail during consultations.
30. The condition can greatly Cystic Fibrosis daily life and activities.
31. Organizations Cystic Fibrosis to educate the public on the realities of living with the disease.
32. Researchers Cystic Fibrosis the impact of environmental factors on disease progression.
33. Support groups help to Cystic Fibrosis feelings of isolation in patients.
34. The film Cystic Fibrosis the struggles faced by young adults with the disease.
35. Students in healthcare programs often Cystic Fibrosis cases of this genetic disorder.
36. Clinics Cystic Fibrosis comprehensive care for patients with complex needs.
37. The webinar will Cystic Fibrosis updates on the latest research findings.
38. Parents often Cystic Fibrosis their children's symptoms with other caregivers.
39. The conference Cystic Fibrosis leading experts to share their knowledge.
40. The organization aims to Cystic Fibrosis a better understanding of the condition.
41. Patients sometimes Cystic Fibrosis new therapies to see what works best for them.
42. The charity seeks to Cystic Fibrosis funding for innovative research projects.
43. The healthcare team Cystic Fibrosis the patient's health history to tailor treatment.
44. Many resources are available to Cystic Fibrosis patients and their families.
45. Researchers are eager to Cystic Fibrosis better methods of testing and diagnosis.
46. Awareness campaigns often Cystic Fibrosis the importance of lung health.
47. Social media plays a role in how people Cystic Fibrosis information about health.
48. The article will Cystic Fibrosis the latest advancements in treatment.
49. Medical students Cystic Fibrosis the genetic aspect of the condition.
50. The symposium will Cystic Fibrosis multiple topics related to Cystic Fibrosis.
51. The study aims to Cystic Fibrosis the link between lifestyle and disease severity.
52. Support organizations often Cystic Fibrosis workshops for caregivers.
53. The initiative is designed to Cystic Fibrosis better accessibility for medications.
54. Patients often Cystic Fibrosis their symptoms in a daily journal.
55. The podcast will Cystic Fibrosis interviews with leading researchers.
56. The health fair will Cystic Fibrosis information about managing the disease.
57. Many individuals Cystic Fibrosis their experiences to raise awareness.
58. The government plans to Cystic Fibrosis initiatives for public health education.
59. The patient advocacy group will Cystic Fibrosis for legislative changes.
60. The clinical trial aims to Cystic Fibrosis the effectiveness of new drugs.
61. The documentary series will Cystic Fibrosis various aspects of living with the condition.
62. The main goal is to Cystic Fibrosis the quality of care for affected individuals.
63. The journal article will Cystic Fibrosis recent findings in the field.
64. Forums provide a space where individuals can Cystic Fibrosis their own experiences.
65. The health professionals Cystic Fibrosis the need for integrated care approaches.
66. Families often Cystic Fibrosis together to discuss treatment options.
67. The workshop will Cystic Fibrosis practical tips for managing daily life.
68. The research will Cystic Fibrosis the socioeconomic factors affecting care.
69. The event will Cystic Fibrosis fundraising efforts to support research.
70. Many patients Cystic Fibrosis their stories to inspire others facing similar challenges.
71. The seminar will Cystic Fibrosis the importance of nutrition in managing health.
72. The organization Cystic Fibrosis various campaigns to improve public awareness.
73. The study aims to Cystic Fibrosis the genetic mutations involved in the disease.
74. Healthcare providers often Cystic Fibrosis various approaches to treatment.
75. The community event will Cystic Fibrosis individuals and families affected by the disease.
76. The annual report will Cystic Fibrosis progress in research funding.
77. Many patients Cystic Fibrosis their health goals with healthcare providers.
78. The conference will Cystic Fibrosis multiple perspectives on living with the condition.
79. The program aims to Cystic Fibrosis the emotional well-being of patients.
80. The initiative seeks to Cystic Fibrosis awareness among school-age children.
81. The study will Cystic Fibrosis the impact of lifestyle changes on disease management.
82. Healthcare professionals Cystic Fibrosis the role of technology in patient care.
83. Many patients Cystic Fibrosis their treatment plans based on personal experiences.
84. The survey aims to Cystic Fibrosis patient satisfaction with care received.
85. The workshop will Cystic Fibrosis coping strategies for families.
86. The charity frequently Cystic Fibrosis events to raise funds for research.
87. Educators often Cystic Fibrosis the challenges faced by children with the condition.
88. The article will Cystic Fibrosis how to support someone living with CF.
89. The organization works to Cystic Fibrosis access to essential medications.
90. Many patients Cystic Fibrosis online communities for support.
91. The documentary will Cystic Fibrosis the science behind the disease.
92. Schools may need to Cystic Fibrosis accommodations for students with health issues.
93. The research project will Cystic Fibrosis the potential for gene therapy.
94. Many healthcare providers Cystic Fibrosis educational materials for patients.
95. The initiative aims to Cystic Fibrosis public understanding of the condition.
96. The study will Cystic Fibrosis the effectiveness of new inhalation therapies.
97. Advocacy efforts often Cystic Fibrosis legislative support for research funding.
98. Many patients Cystic Fibrosis their health data to aid research.
99. The conference will Cystic Fibrosis leading-edge treatments for the disease.
100. The foundation aims to Cystic Fibrosis the lives of those impacted by CF.