Trusted Resources: Evidence & Education
Scientific literature and patient education texts
	Sickle Cell Disease and Sexuality
	source: St. Jude Children’s Research Hospital
year: N/A
summary/abstract:Several diseases can be spread when people have sex. They are called sexually transmitted diseases (STDs). These diseases are common in teenagers and young adults. Some teens today are having sex at an early age. They may even have more than one sex partner, and they are not always using protection. For these reasons, STDs are a growing problem in people under the age of 25.
Teens and young adults with sickle cell disease can make and have babies. If you choose to have sex and you do not want to have children, you must use birth control. Both males and females need to think about birth control. The only form of birth control that will prevent both pregnancy and STDs is a condom with a spermicide. A condom looks like a long balloon that is placed over a man’s penis. Spermicide is a foam, cream, or jelly, which contains chemicals that kill sperm.
read moreRelated Content
- 
                                                                    
                            
                        
                        
                                                    Sickle Cell Community-Wide Support & Empowerment Group (Nov)Sickle Cell Community-Wide Support &...
- 
                                                                    
                            
                        
                        
                                                    Introducing: The I Believe in Therapy Campaignhttps://www.youtube.com/watch?v=KsHqXvAF...
- 
                                                                    
                            
                        
                        
                                                    Parent Perspectives on Pain Management in Preschool-Age Children With Sickle Cell DiseasePain episodes occur for many preschooler...
- 
                                                                    
                            
                        
                        
                                                    The challenges of being a caregiver to my cousin with sickle cellWhen I embarked on this journey as a c...
- 
                                                                    
                            
                        
                        
                                                    Implementation of the NCAA sickle cell trait screening policy: A survey of athletic staff and student-athletesObjective: To describe the perspectives...
- 
                                                                    
                            
                        
                        
                                                    The Bad Blood: My Life With Sickle Cell AnaemiaI wake up with an active volcano for a c...
- 
                                                                    
                            
                        
                        
                                                    KNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
 
		    Google
 Google 
                 
		 
	   +myBinder
 +myBinder 
					