https://community.usms.org/swimming/f/general/12091/wolff-parkinson-white-syndromehey my name is Ariel and I&#39;m 20 years old and I&#39;m swimming more than a decade. and after all these years that I trained no one had diagnosed my WPW until now, and i wanted to asked from you guys if you think that is it the right decision to do thaten-USTelligent Community 12https://community.usms.org/thread/194810?ContentTypeID=1Sun, 15 Mar 2015 10:21:54 GMT3187ac58-ba85-4314-b79a-c45cd885e09a:00ab57ba-0dad-44ae-8f8b-ba4f29d52b1aFormer MemberIf you have experienced tachycardia, then you should definitely have the ablation. It is a catheter-based procedure with a 100% cure rate. You should be able to continue swimming without any restrictions.<div style="clear:both;"></div>https://community.usms.org/thread/194799?ContentTypeID=1Sun, 15 Mar 2015 05:38:25 GMT3187ac58-ba85-4314-b79a-c45cd885e09a:97f92831-5f81-4eae-9251-01b524b93ca1BobinatorHmmmm, I&#39;d talk to my Doctor and go with her/his advice. I have LQT which may be one of the 14 diseases in the same group as WP. I had genetic testing done and my variation did not fall into any of the current types out there. My family is currently being studied by a group of EP&#39;s and per their advice I&#39;m taking beta-blockers (great for swimming, not) Seriously, find a EP or Cardiologist you can relate with and hash it out with them. I wouldn&#39;t want a layman&#39;s opinion in topics so important to my life.<div style="clear:both;"></div>