Hi all Does anybody on the forum suffer from Wolff parkinson white and POTS? If so, has anybody had ablation surgery for the WPW? Did this affect your POTS at all and if so how? What medications have you found useful/not useful? So many questions I know! I am feeling so overwhelmed at the moment. Since my last post of being admitted into ICU for shortness of breath, the doctors discovered arrhythmia due to what they now believe is Wolff Parkinson white. It seems the medication I was on for my POTS was making the WPW worse. Is it possible for WPW to be missed on ECG and only picked up now after numerous ECGs, holters etc? I have been put on new medication for the WPW. The doctor has given me verapamil but the problem with this is that it leads to further hypotension and with my POTS...I need not say more...I really feel horrible. From being fairly in control of my POTS to now not even being able to get up without support, diarrhea two to three times a day and just complete exhaustion... Has anybody else ever had these two together and if so please give some info!