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jjnfc

Hi all. I just found this site yesterday and have been reading as much as I can. I was told last Thursday that I need a mitral valve replaced. I had been told I had regurgitation and that we were watching it but in my mind I was thinking possibly years down the road before I'm faced with it. Guess what?
I have been comparatively healthy all my life but in June of 2004 started experiencing light headedness and weakness and discovered I had bradycardia and had a pacemaker installed. The doctors were pretty much inconclusive as to what caused my problem, possibly at one time in my life maybe an infection. I did have a small area of sarcoidosis in one lung and took steroid treatment for 6 months. That quickly disappeared and I was never aware that it was even there until I went in with my slow heart rate. My doctor says the bottom part of my heart is stiff and doesn't flex as well as the rest of my heart does. I had taken Pondimin a few years ago when it was all the rage. My doctor says that is not my problem but it is on my list of questions to ask on the next visit (16th) as to why he is so sure that it isn't. Anyway, when we meet on the 16th we are to discuss a possible surgery and I am just like a lot of the other theads that I have seen, scared, upset, mad, actually I feel like I am in the Twilight Zone. Today is my 50th birthday and I want to be giving advice to the new ones on this site when I'm still 100. I can already see that you all are going to be a lot of support and comfort. Anyone that maybe has something similar, possibly that is sarcoid related or Pondimin use I would appreciate hearing what you have to say. Thank goodness I don't have a lot of the symptoms yet, which confused me at first because I thought I should wait until then and do something about it. Now I see that the sooner you can correct the problem the better off you will be. I do have some fatigue, lots of PVC's (I think the pacemaker adds to that). I seem to feel great one minute and then be bottomed out and then feel pretty good again a little later. So far no swelling, just a fullness, out of breath type feeling when I eat, some lightheadedness. I'm still able to get out and walk a couple of miles and do yardwork, vacuuming, etc. Any comments or advice would be greatly appreciated. Thank you.
 
Welcome Jannette and Happy Birthday.
You will get all the support you need here even if we may not have all the answers you seek.
It is generally thought that having surgery before the heart is permanently damaged is the way to go. Only your doctors can make that call but be sure and push back if you feel you are not getting all the answers you want.
The biggest decision you will have to make, once surgery is decided, is the type of valve you want. Getting through surgery is a long road but one that will be lined with people wanting to help.
Best of luck on the journey.
 
Thanks so much, I feel better already. Just reading all of your posts has been very helpful and being able to discuss with people that have been in the same shoes. My first thoughts when I found out was that I wanted to talk to someone that has been through this before and here you all are.
Thanks again. I will keep in touch.:)
 
Welcome Jannette! I had my mitral valve replaced 14 years ago at the age of 32. It is a life changing surgery - the biggest change is that you appreciate life so much more.

Your arrhythmia may also be due to your mitral valve. The mitral valve is infamous for causing arrhythmia. That was my biggest problem before I had the valve replaced.

I'm glad you found us and we hope you'll be around at 100 giving advice too!:D
 
Tewdew, tewdew........tewdew, tewdew........

Tewdew, tewdew........tewdew, tewdew........

jjnfc said:
actually I feel like I am in the Twilight Zone. Today is my 50th birthday and I want to be giving advice to the new ones on this site when I'm still 100. .

Yes, it is surreal at first. Just wanted to welcome you to the group and send hugs. You will be doing just that at a hundred. Katie will be right there with you at age 55. I will sadly be gone as she is going to put me in an early grave. heehee! :D Many hugs. janet
 
gijanet said:
Yes, it is surreal at first. Just wanted to welcome you to the group and send hugs. You will be doing just that at a hundred. Katie will be right there with you at age 55. I will sadly be gone as she is going to put me in an early grave. heehee! :D Many hugs. janet
Janet,
It sounds so funny to picture Katie as a prim and proper 55 year old. I am sure she will still be kicking butt and cute as a button but I still see her face and it looks odd on a middle-aged woman.;) :D ;)
 
jjnfc said:
Hi all. I just found this site yesterday and have been reading as much as I can. I was told last Thursday that I need a mitral valve replaced. I had been told I had regurgitation and that we were watching it but in my mind I was thinking possibly years down the road before I'm faced with it. Guess what?
I have been comparatively healthy all my life but in June of 2004 started experiencing light headedness and weakness and discovered I had bradycardia and had a pacemaker installed. The doctors were pretty much inconclusive as to what caused my problem, possibly at one time in my life maybe an infection. I did have a small area of sarcoidosis in one lung and took steroid treatment for 6 months. That quickly disappeared and I was never aware that it was even there until I went in with my slow heart rate. My doctor says the bottom part of my heart is stiff and doesn't flex as well as the rest of my heart does. I had taken Pondimin a few years ago when it was all the rage. My doctor says that is not my problem but it is on my list of questions to ask on the next visit (16th) as to why he is so sure that it isn't. Anyway, when we meet on the 16th we are to discuss a possible surgery and I am just like a lot of the other theads that I have seen, scared, upset, mad, actually I feel like I am in the Twilight Zone. Today is my 50th birthday and I want to be giving advice to the new ones on this site when I'm still 100. I can already see that you all are going to be a lot of support and comfort. Anyone that maybe has something similar, possibly that is sarcoid related or Pondimin use I would appreciate hearing what you have to say. Thank goodness I don't have a lot of the symptoms yet, which confused me at first because I thought I should wait until then and do something about it. Now I see that the sooner you can correct the problem the better off you will be. I do have some fatigue, lots of PVC's (I think the pacemaker adds to that). I seem to feel great one minute and then be bottomed out and then feel pretty good again a little later. So far no swelling, just a fullness, out of breath type feeling when I eat, some lightheadedness. I'm still able to get out and walk a couple of miles and do yardwork, vacuuming, etc. Any comments or advice would be greatly appreciated. Thank you.
hi welcome you,ve come to right spot for support
 
Happy Happy Happy

Happy Happy Happy

Welcome to VR.com and I hope you have a wonderful birthday:D
 
On the good ship VR.Com!

On the good ship VR.Com!

Jannette,
Welcome to another passenger on the lifeboat, VR.Com.;)
Put your life jacket on, grab an oar, and and feel free to pitch in and help your fellow travelers!:)
 
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