1st diagnosed in 1960

Hi, In 1960 I was told by my family Dr that I should see a Cardio Dr cause my HR was very low, 40-45. That is when I was told I had a COMPLETE heart block (completely missing the electrical connection between the upper and lower chambers) and because of my previous style of life, it was conjenitial. Nothing was suggested to do at that time. Now jump up to 1979, when after moving to CA it was again suggested that I see a Cardio Dr. He took a very strong interest in my condition. At that time he said their was only about 20 of us in the US (seems like much more with this forum) that are surviving with this condition, and we were helping them write the info in the medical journal. In 2002 he called me and said that 1 of 'us' had been playing tennis, stopped, and during the hearts 30 sec recovery period, he passed out. EMT'S placed an external Pacer, implanted in hospital. Said that after stress test during 30 sec recovery, all of our EKG's looked the same, like a seismograph reading. All concerned Dr's then thought this was normal, cause we were all the same. Normal, but possibly not in our favor.
When I was asleep, my HR dropped to 26-27bpm, normalday 35-40, BP was allways on the very low side. He suggested a Pacer. The battery lasted, 2002-2009, when a replacement Dr implanted an ICD. Also during this period of time I would go in and out of A-fib frequently, so far med's can't correct this. I don't have any symtons with Afib, they read it of my ICD.
I don't know (my Dr either) if I would still be alive today without the Pacer's, but I am. I am 73 yr's old, and even without the heart block, in the 60's, who would have thought I would have lived this long??


3 Comments

Amazing.

by Duke999 - 2014-03-27 06:03:34

That you are.

I wish you continue doing well.

Duke

CCHB

by Tracey_E - 2014-03-27 10:03:19

Very cool story, thanks for sharing! We have a few members who have had pm's for CCHB for 30+ years but I don't think any of them are older than 60-ish. I got my first one in 1994, am on #4 now and feeling great.

I think there are a LOT more of us than they used to suspect. If we don't have symptoms- and because our bodies are used to compensating and getting by in block, many of us do not have symptoms for years- the only way to diagnose is if we happen to be in block when on a ekg. My pediatrician noticed my hr was very slow (44, always, no matter what) when I was 5, that was in 1971. They just watched me until I went downhill in my early 20's. Now, they pick it up on the prenatal ultrasound so moms know their babies have it well before birth. I don't think there are more cases, I think there are just more diagnosed.

Welcome, so glad you found us!

Still pacing after all these years

by pacerpostergal - 2014-03-29 07:03:01

How-do-you-do, all PM Clubers! I guess I'm the newbie here, however no newbie at all to the wild, at times whacky, and wonderful world of pacers. Proud and very blessed to be "60ish", after living with CHB and pacer dependency since 1971, when I got my first PM implanted at age 18. Back then, pacers were the size of a cigarette pack! Their bells and whistles were few, but I remember one model I had lasted for 13 years.

Flash forward 43 years-4 years since my last generator change. I lost count years ago on how many PMs I've had (so far!), and the maze of leads that remain within my chest today. I've birthed and raised 3 wonderful daughters, and have my first granddaughter on the way!

43 years ago while I lay in a hospital bed in Boston, groggy on pain med just after just getting my first PM, my former b/f knelt by my side and said goodbye after making sure I was OK. I never saw him again until he found me on the internet in 2011 - he was living in WA state and me in CA. We are together again and he just received HIS first PM this past September! We are lucky to have the same wonderful EP specialist looking after us!

Forever grateful to God and science,

Karly

You know you're wired when...

You can hear your heartbeat in your cell phone.

Member Quotes

I have an ICD which is both a pacer/defib. I have no problems with mine and it has saved my life.