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Advice please!

So I hope that one of you out can give me some advice and cheer me up a little. Most of you know my story by now. My last surgery was four weeks ago today nothing big just another ablation. So somebody please help me understand why I still feel no good. I still continue to have no energy in a way I think the doctors got my hopes up saying in two weeks your life should be back to normal and you can do anything.
I've been getting dizzy a lot more than I was, having a lot of spasms and its...

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Hello again

Hi all, hope that you are all doing well. I posted on this site a few weeks back as i had just found out that I needed a PM, i know have my date which is July 30. I am starting to get quite nervous and I no realise that i am about to get one.

This site has been so much help to me. I think it will be very important over the next few weeks.

Well you will be seeing alot more of me in the next few weeks.

Fiona

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Latest Lamb News

Hi folks

Our little one passed away yesterday. We called her Bluey because she wore a blue jumper. The weather has been so bad cold and frosty and now it is wet with a bad wind chill factor.
The sheep actually belong to the farm next door. Each year they give birth in the paddock next to our house. It is like a birthing ward with Ewes grunting and groaning just like us ladies giving birth. As we can hear them at night I just cannot bear it when the little ones get seperated...

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New From England

Hi My name is Eileen and i am from England. I have a De-Fib/Pacemaker and have a condition called non-compaction. Episodes of VT. I have lots of eptopic beats and pulputations. I am now 29 years old. Does anyone have the same as me or similar.?

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Still in hot pursuit...of a diagnosis

Hello again everyone! I am still trying to get a diagnosis for my arm swelling and pain. I have since graduated to increased pain meds including motrin and percocet taken together. The swelling is no different. Been to a second ER by pacer guy. The ER staff read the pacer doc's notes (which include his denial of pacer involvement in my symptoms which started after it was implanted) and went on that. I was sent home again with only additional pain meds....and, by the way, a documented fever now.<...

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MOM OF SON WITH PACEMAKER

MY SON HAS HAD HIS PACEMAKER SINCE THE AGE OF 5. HE HAS TOTAL HEART BLOCK. WE WERE NEVER GIVEN AN ANSWER AS TO WHY THIS HAPPENED. THERE IS NO FAMILY HISTORY. MY SON MICHAEL HAS HAD A TOUGH TIME THROUGH THE YEARS. HIS FIRST PM WAS IMPLANTED A WEEK AFTER HIS FIFTH BIRTHDAY, A FEW WEEKS LATER MY HUSBAND AND I FOUND OURSELVES DRIVING HIM BACK TO THE HOSPITAL ONLY TO HAVE HIM SLIP INTO A COMA ON OUR WAY THERE. HE WOUND UP WITH A STAPH AURES INFECTION. HE WAS IN THE HOSPITAL FOR ALMOST 3 MONTHS AND WO...

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Free Replacement

My Grandfather was implanted a pacemaker from Shree Pacetronix, an Indian company almost 8 years back and is working fine.He wants to move to USA . I want to know if the pacemaker company's in USA also give Free Life Time Warranty replacement there on the Pacemakers implanted because the company in India does. If any one knows let me know as most of the companies do give Free Replacment in India but I think if you are living in USA or Europe they do not provide the same warranty. If they don't...

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Yet another reason I love my pacemaker

We have recently completed a trip. I love my Pacemaker. At the airport the line projection was almost an hour. However, since I have my special patdown procedure, no waiting. We went to special assist and got head of line privledges, even over all of the special first class passangers.


YEAH. See it is cool sometimes.

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ICD WebRing

Would like to hear from all of you. I am starting an ICD WebRing if anyone is interested in more exposure for heart disease.
www.jimsjems9.com/icdring.html
It's good to know I am not alone in my experiences.

JimsJems, Mayor
hometownusa@jimsjems9.com
www.jimsjems9.com/

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Bastille Day.

Hello Everyone.

Today in France, is Bastille day, our version of the 4th of July. Here is a little bit of history.

Bastille Day is the French national holiday, celebrated on 14 July each year. In France, it is called "Fête Nationale" ("National Holiday"), in official parlance, or more commonly "quatorze juillet" ("14th of July"). It commemorates the 1790 Fête de la Fédération, held on the first anniversary of the storming of the Bastille on 14 July 1789; the storming of th...

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Thankful for PM Club

Hello,

I can't t tell you how much this pm club has helped me. I am still resting quiet a bit and I am finding that I look forward to getting on and reading everyones story. My laptop has been my best friend since my heart surgery in Nov. and the the pm in June. I have not been able to get out unless I have more tests to go to or Dr. appt. I feel like I just found a lot of friends! One's that understand and their experiences have help me to know some of my feelings are normal. Thank...

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starting to feel better after 6 weeks.

I'm staring to feel better after getting my PM 6 weeks ago.When I felt like I was short of breath and had difficulty climbing stairs my cardiologist had me do a nuclear stress test. I lasted 50 seconds on the treadmill. The stress showed that there might be a "mild" blockage so the cardiologist wants me to do a catheterization. It is scheduled for the 17th of July (next tuesday). Afew days ago I played golf and felt pretty good.
I was able to take a 2 mile walk today and walked up the stair...

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radiation

Hi, I have just received news that I have breast cancer, I am totaly dependent on my pacemaker and because of the heart problems the doctor said this is not the type of cancer that spreads, but I am wondering, if the time comes if I can have radiation, they cannot put me on Tamoxifen because of the heart and on cumandin

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Pain

Hi! I'm twenty years old and am having problems with my pacer. It is a dual chamber, but not a defibrillator. I had the pacemaker implanted in January of 2006. After a lot of pain, I had it relocated to be deeper under the muscle in November of 2007. I was doing okay for a while, but now it's coming back, worse than ever. I have an awful pain on the left side of my chest above my breast where the cite is. The pain also goes right below my underarm on my left side. The pain has recently been radi...

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oops

Wrong years, I apologize. It was first implanted January of 2006 and then relocated in November of 2006 as well.

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Football

Someone mentioned playing football 3 times a week. Is that full contact tackle? My son is considering playing high school football. Has anyone else done that - any problems?

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~ *I*R*I*S*H* *P*A*C*E*R*S* ~

Hello,

Just wondering whether any Irish Pacers would be interested in getting together for a drink, meal and good chat or just general support. We have a pacer in Dalkey (Hi Rob!) who knows a good venue, but I'm sure this can be discussed futher. Please let me know if anyone is interested, there's 3 of us so far (from Dalkey, Donegal and Galway) but there must be more of you out there ........... drop me a line with any thoughts, thanks and look forward to hearing from you ......

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Will I always be thinking about my pc?

Hi, I'm 49 and got my pc on June 28th. I am not so aware of it at home but am leary about going out. When i have gone out I feel the need to put my hand over my pc as I feel it 10 times more. I feel the weight,skin tight and slight pains. Is this normal? I haven't been back for my 1st pc check yet so I feel stupid asking them these things as I'm sure they think it's all in my head. Probably right about some of it. How long before you guys started driving? I have MVP,CHF, restrictive cardiomathy...

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aware of pacing most of the time

Just wanted to know if anyone else is very aware of their pacemaker. Mine feels like it is going to jump out of my chest sometimes and I feel it most of the time. I have had an AV node ablation and the tech said I was in A-Fib all the time now.Had it implanted in August-2006. My voltage is set at 3.50. My doctor says that I am just super sensitive.

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Short of breath....

It's been almost 5 weeks since my pacemaker was implanted and I am getting short of breath. I already have CFS and was short of breath then, but, this time it's worse. If I'm up for maybe 3 or 4 minutes then I get pressure in my head and feel light-headed and short of breath until I can sit down.

It doesn't happen all of the time. Maybe 3/4 of the time.

I am wondering if it could be my nerves? I'm taking Clonazepam 0.5 mg tablet 2x daily for anxiety. I understand that this...

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You know you're wired when...

You always run anti-virus software.

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