Introducing me...

Hello All,

I am so happy I found this place!!! I am a 45 year old mother of three, 23, 16, and 9. Three years ago, I passed out and went code blue in the right place at the right time! In the hospital. I was being monitored for possible heart attack. I never had the heart attack, which is a good thing.

After going Code Blue, I then went into A-Fib. It took three kinds of meds to get me back going again. The next day... the doctors came in and asked me if I had ever had that happen before.
My answer was fairly fast.... I'd been passing out all my life, from my early teens onward. It let up during my 30's and that was the first time I'd passed out in my 40's. I was never aware of going "Code Blue" or of "A-Fib" in myself.

I was soon, diagnosed with Sick Sinus Syndrome and told that I needed a pacemaker. And the next day I got one... April 30, 2004. I was given great care at the hospital, but had many questions. My cardiologist was great, but there was never enough time to ask all the questions I had.

Anyways, I have a Medtronic EnPluse with dual leads... I tell people I have "dualies" LOL. And btw, the Medtronic guy was great!!!!

Apparently I have a very small heart and a small cavity, my pacemaker was hard to place. One of the leads punctured a hole in the sac around my heart, and I had symptoms. I kept going to the regular doctor telling her I had asthma and she kept telling me it was my heart. I didn't see the connection, and kept insisting an inhaler! Finally when I had so much liquid around my heart that I passed out when sneezing, or trying to pick up my daughters toys.... (I couldn't bend over anymore)... and I sneezed on the job and fell over... finally I called the heart doctor and he told me to get in there. They did an ultrasound and had me go straight to surgery in the hospital. When they laid me down to drain the fluid, I went code blue again.... They drained 2 liters of fluid out from around my heart. Of course, I was in the hospital for a few days. It was during this time, that I decided that a "Friend" of mine, who was very close to being a "boyfriend" already--well, he became my boyfriend. I've fretted and fretted..over ethics and doing things right all my life. I didn't want to hurt somene by going into a rebound relationship, but I felt this was so right. Looking at my mortality straight in the face, I kind of threw out the rights and wrongs...and said, "please let's try"

This guy is now my husband, We've been married over two years now. He just had a six way by pass in October. We knew when we married that each of us had special history --his father died at 34 of his third heart attack. At that time, no one had yet come up with open heart surgery. When I met him, he had had two minor heart attacks, had two stents, high blood pressure, and had just been diagnosed with diabetes. My father died at 43, his first heart attack at 32 killed 1/2 his heart, but he had the benefit of open heart surgery and lived another 10 years. I'd been waiting my whole life to have a heart attack like dad, and die young. I have always lived my life pretty much like each day is the last... and so does my husband.

Once, I was healed up from the fluid being in that sac, I can honestly say that for the most part I've had no problems. Once in awhile, I swear I can feel it zap me, and I just figure it's doing it's job. Last night it zapped twice, very hard, so hard it made my stomach upset. I don't know if it's normal, but I figure as long as it's keeping me alive, It's okay.

My first cardiologist's office, would test me, and tell me how the pacer was doing and let me know when I used it, how often, etc. I found the information useful and also it helped me to feel better about myself because I was only using it 1-2% of the time.

My new dr. checks me via phone, and all I hear is that the pacer is doing well. I don't like this. I want to know if my usage rate is going up or not. I really don't know if I have the right to ask.

I've done lot's of research on Sick Sinus Syndrome and gotta say, I don't really understand all of it. One thing that has had me curious this whole time is about when my heart will just stop, and the pacer won't be able to help. Can I go on for years and years this way... can I get old??? I mean... if I don't have a heart attack.. or other things like that. Right now, I'm in fairly good shape, and have not developed full blown heart disease. I"ve had high blood pressure since I was in my 20's, it's inherited, and I was finally diagnosed and put on meds when I was 28 (after years of headaches, etc.). I am just now starting to show damage from that.

I'd love to hear from others, no matter what your experiences...
I love reading here, I've learned so much. I've even read some things that might help my husband (he had a golf ball sized lump on his lower sternum, that is very painful--I read something here that made me wonder if it's scar tissue that can be relieved).

Thank you so much to those who started this club, maintain it, and publize it. Thank you to the members who participate and help folks like me who come along! This is just great and would have been so helpful to find months, and months, if not a few years ago!!

Thank you--
Peggy S.
Myrtle Creek, OR


4 Comments

Wow!

by hooimom - 2007-10-07 03:10:58

Hi Peggy,

First I said wow because your kids are spaced from 23 to 9. Then I said wow because of fainting your entire life. Then a louder wow came when I got to the fluid around your heart that was missed for so long. Okay, I won't say how many times I actually said wow while reading your post!

The only bit of wisdom or advice I have to share is that you have the right to ask any question whether it is with a phone interrogation or a doctor's appointment. Ask anything and everything that you can think of to ask. Make lists and take them with you. Your doctor should be willing to answer all of them.

I am glad you found the site. It is a wonderful source of information and encouragement. Thanks for sharing your story!

Michelle

Amazing

by ela-girl - 2007-10-07 05:10:37

I am with Michelle on this...I can't remember how many times I said WOW or WHOA while reading your post! You have had to overcome a lot in your life just by what you inherited.

And I don't really have anything different to add to what Michelle said. DEFINITELY ask any question you want. It is YOUR health you are inquiring about. You have a right to know everything. And you can even ask for copies of your records and keep them in a file at home. Doctors can't deny you that access because of the HIPPA law. You and your doctor work as a team to keep you healthy, so definitely seek answers to your questions.

On a side note...I am 30 and my little sister turns 10 tomorrow. So, I think it's cool you have kids who are spaced apart!

Hope to see you around on the site!
ela-girl

Double WOW

by Carol - 2007-10-07 08:10:46

I'm a new "pacee", but ditto to everyone else's comments. I am a registered nurse and would like to comment on your statement about having the right to ask your Doc questions. Please remember that in essence our Doctors "work" for us and we certainly have the right to ask questions regarding our health. When you make your appt. let the scheduler know you have many questions-hopefully he/she will schedule a little more time. My next suggestion is WRITE those questions down...I am a nurse and work with doctors everyday, but when I'm in the office about ME I have to have a list, because I'm human and get flustered too! So ask away, no question is too foolish. It IS a big deal to us and I can tell you, now that I have a PM, I believe it will help me be a kinder more compassionate nurse with my patients who "just had a pacemaker...no big deal" Blessings, Carol

Hi Peggy

by taylorct - 2007-10-22 07:10:50

It looks like you've had an interesting life! I'm happy to hear that everything has worked out for the best. The questions you ask are a lot of the questions I find myself asking frequently. I am 19 years old and have had my pacemaker since I was 15. I had zero health problems when everything happened. You said you wanted stories, I've been told I have a pretty good one so here it is...
Easter Sunday of 2001 I was at my grandma's and got up to put the dishes away after dinner when I felt the worst pain ever, I was only 15 at this point so it didn't occur to me that it could be a heart attack. It felt like my heart was getting tighter and tighter and I couldn't catch my breath. A lot of the time when I stand up I start to black out a little because I had a slow heart rate anyway so when everything started going black I thought it would pass. It didn't. I fainted and when I woke up had my parents and grandma in quite a frenzy. The next day I was scheduled to get blood work and a heart moniter put on for a day. First I received the heart moniter and went to get blood work. While they were sticking me with needles, I passed out again. I had no chest pain this time. Three days later was I called out of school to come to the hospital immediatly. A doctor from Iowa City had come into town to talk to me. ( Iowa City has the best hospital in the state.) He then showed me the results from my heart moniter, 10 minutes after having it attached my heart had stopped beating for 21 seconds. The next day my pacemaker was implanted. A top cardiologist came down from Minnesota just to talk to me because I seemed to be some sort of miracle, he told me he had already presented my case to his classes. I'm still an undiagnosed mystery though! I am the proud holder of a record of the longest pause of a heart though.I have no idea why any of this happened to me or why my heart started back up after stopping for so long. I am extremely thankful for the mysteries of life. I wonder everyday if my heart is going to stop again. How do I know the pacemaker will keep it going? I guess we just have to have faith in things like that. It still hasn't hit me. 4 years later, how close I came to dying and I'm sure some day it's all going to hit me. It hasn't seemed to impact me much, but people have expressed to me that I am an inspiration to them. My track coach told me I have changed his life and some of the nurses at my home clinic told me the same thing. I don't think I'm much different than anyone else, I'm sure if anyone had to get a pacemaker they would do it and continue their lives like I have, but if I can make other people feel better I'm not complaining!

That was much longer than I meant for it to be, sorry! I don't get a chance to talk much about all this to other people... Thanks for letting me tell you my story!

Taylor

You know you're wired when...

You trust technology more than your heart.

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