Wolf's Parkinson's White Syndrome/Heart Disease

Rapid Heart Beat/Heart/Heart Blockage Palpitations/Supraventricular Tachycardia

Wolf Parkinson's White Syndrome is a rare disease affecting mostly males. I first heard of this disease of the heart when a friend of mine's son contracted the disease. He was a freshman in college and had been complaining
 of feeling tired and "somewhat dizzy" followed by his heart beating rapidly. After coming home and going to the doctor,he was given iron for anemia, and antibiotics for a virus, his mother said. He went back to college expecting to feel like his old self soon. Instead, a few months later he collasped in the classroom. He was diagnosed with Wolf Parkinson WHite Syndrome. I thought to myself, what the heck is that? My curiosity about this disease, resulted in the writing of this article. 

I am writing this article from a layman's understanding of what is Wolf Parkinson's White Syndrome. The heart has four chambers, two at the top call atria and two at the bottom called ventricles. The sinus node is the heart's natural pacemaker. It is located in the heart's right atrium. It gives off electrical impulses to make the heart beat. In order for the heart to beat properly, the signal must travel down a specific path from the sinus node to the ventricles. As long as the impulse is trasnmitted normally, the heart pumps and beats at a regular pace. Sometimes the signal from the heart's upper chambers to the lower chambers is impaired or doesn't transmit. This is when heart block occurs. 

Wolf Parkinson's White Syndrome increases the heart rate by blocking the normal conduction system. It creates an abnormally fast electrical conduction in an accessory pathway within the heart bypassing and blocking the normal conduction system. 

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I have wpw i was diagnosed 2 weeks after birth and i am almost 18 and i am ready for the surgery to correct it do they keep you awake during the surgery or do they put you under?

Posted on 10/22/2008 at 2:10:47 PM

My son has had this disease and i think you should take it very serioously because you can have a heart attack from it . My son had to get a pace maker to make the heart function properly. God Bless

Posted on 07/22/2008 at 8:07:54 AM

I have/had WPW. i was released from the hospital yesterday after basically dieing from it. I had it my whole life and it never showed any symptoms until monday night when I was at work.. My heart was pounding through my chest i was faint and dizzy. I drove to the emergency room where they had to immediately defibrillate me. The doctor said that it is a miracle that I am even alive. I flatlined multiple times on the operation table but the ablation was finally successful and i am 100% CURED. You can have this disease your entire life and not even know it until you are knocking on heavens door. The doctors told me that I am not supposed to be alive, I am now just counting my blessings and I am happy to still be here.

Posted on 05/01/2008 at 12:05:34 AM

My father has this, and I suspect I do as well, for the last 12 years i have had rapid uncontrolled skipping, it causes pain and often I feel like I might faint. :( I have seen the doctor numerous times and have heard everything from its nothing, its you IUD and oh you do have an irregular heart beat but its no big deal your fine. I keep saying if I die from a heart attack I hope my kids sue the doctor! It is really unclear to me why i pay so much for health insurance, co-pays and time off work to have to tell my doctor what is wrong with me. In addition my father, grandfather and I all have tremors, my dad has had some luck with enderol

Posted on 02/20/2008 at 6:02:27 PM

Hi All, I was diagnosed with WPW 10 yrs ago but it looks like I have had it since I was a kid. I am now 43. I had an episode 2 days ago and it looks like I go in on Friday to have the ablation. Even if it gives me a few years of relief from this I would be happy. Thank you for posting this info as it has helped so many people Good Luck to all

Posted on 02/13/2008 at 4:02:06 PM

Thanks to all of you for posting your comments. My niece was just diagnosed. It saddens me to hear, though, that some of you have had the surgery and it came back. Tell me, is the surgery painful?

Posted on 02/13/2008 at 2:02:16 PM

i was 22 weeks pregant when they picked up on ultra sound that my son had it .my son who is now 10 year old has had a few problems but hasnt been in hospital since he was 4 weeks old.it was actually good to know that some other people do have it cause here in australia not many people have heard of it .

Posted on 02/07/2008 at 3:02:40 AM

We've been to the Doctors office so many times in 2 different statew whithin the past 2-3 years and every doctor kept telling us "i dont know what's wrong she's healthy" but she kept having these palpitations. and now we're in alaska and we went to the doctor 2 days ago and this is what she said that my sister might have. We were pretty releaved to find out that somebody thinks they know what is wrong with my little sister's heart. For right now though, she perscribed acid reflux pills just in case it's not that serious. This article is great and really explains this so you can understand instead of using the big doctor words. Thank you to whoever wrote this article.

Posted on 01/19/2008 at 10:01:30 AM

ive had this for a few years it showed up when i was young and i dont know whats going on no one ever took the time to explain it to me thanks for putting this here it helped me.

Posted on 01/12/2008 at 7:01:40 PM

I was diagnosed with wpw after many trips to the ER in June 06. I had ablasion done on July 5 07. Never have any symptoms and my ecgs all come out clear. Good luck to all of you, there is a cure.

Posted on 01/04/2008 at 2:01:48 AM

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