Intro/Coping

Hi guys! This is a dual intro/coping post! I happened to stumble on this by sheer luck and I'm really surprised to have found it!  Anyway, my name is Megan , I'm 26 years old from NJ and had my pacemaker inserted in an emergency procedure January 25, 2017 (a Boston Scientific I think my model is Accolade)I was diagnosed with Inappropriate Sinus Tachycardia in Summer '16 after running in the 200s for several days straight. I totally flunked my stress test (walking a slow rate shot me to 210. BPM). I had to do a transtelephonic halter monitor and carry an extra cell and press whenever I had an issue for 12 days. 12 days later I got the IST diagnosis and placed on Corlanor. I did fantastic on it, except about 5 months later I started having sever episodes of bradycardia with symptoms. Doc said when my rate was low don't take the meds for a day. And then all of a sudden december hits and January and I continuously run in the 20s/30s (sometimes i'd be normal 70s too).  My local docs and hospitals couldn't help me - so I take a 2.5 hour journey out to Temple University Hospital and meet Doctor Cooper.  He schedules me for a pacemaker Feb 1 and needless to say I didn't make it to that day and got admitted January 24 and an emergency pacemaker Jan 25. Needless to say, I've had some issues - I get a pain in my left shoulder SO badly now and it seems (reading the other posts) it's normal haha. 

I guess I find the biggest issue I have now is coping with having the pacemaker in the first place. I'm 26, I love kickboxing, I love exercise - I just never understood how I could end up with a pacemaker at 26. I never saw it coming, a lot of people my age don't understand because no one has it. I suddenly felt like I aged a lot and it sounds dramatic but after ending up with an emergency procedure (2016 was a terrible year hahaha) I just have a hard time grasping "why?" I know I'm lucky to have this shot to have a better life, but I just am having a hard time even dealing with that I have this in the first place. 

 

Anyone else out there have a hard time grasping the concept ?  My family hasn't been much help with it because none of them have any heart issues and I find a lot of people saying "you're too young you don't need that." And that's pretty frustrating. Just wondering on some tips and tricks to help cope with it all! 

 

Thanks guys, lovely to meet you all!

 

Happy Pacing!


5 Comments

Young folks

by Hamsquatch - 2017-02-12 23:41:42

Hi Megan, I was 28 when I had my ICD implanted so I can relate. It definitely isn't ideal but the alternative is less so. People our age don't get it, most people don't get it and unless you've been in a life threatening situation you probably won't get it. I get generic responses similar to you "haha you're too young for that" because people....don't get it! Maybe try to educate your family, if they were with you part of your hospital visits they should have some understanding, honestly my mom freaked out about it more than I did.....I just felt "if I die I die theres nothing I can do about it". I also feel it aged me both physically and mentally, physically....well I'm basically an old man with an ICD and take a cocktail of medications and mentally like there's not enough time on this earth to beat around the bush and I try to be dead honest with people without being rude. 

As for your shoulder, still use the arm just follow to precautions, I'm just over 2 years post surgery and my should/rotator cuff feel buggered. 

And 200bpm for several days is nuts! 

23 Here!

by robinclaire93 - 2017-02-12 23:43:00

You're not the only one! I am 23, and a mother of two little boys! I never knew I had a problem until I was pregnant with my first at 18, and apparently had it my entire life! I had sinus bradycardia with 2ND degree AV block. My normal was 30's and 20's when sleeping. I put the surgery off until my doctor wouldn't let me any longer. I had a Boston scientific put in September 19th 2016. He put it kind of under my arm so I could still wear tank tops and stuff. I do know exactly how you feel about nobody really understanding. When I tell people I have one, their exact words are You're too young for that! Or just a look of total disbelief. You can message me anytime. It would be nice to have someone my age to talk with about it since we are both pretty new at this. :) 

PM

by TheLetterM - 2017-02-12 23:58:24

Thank you guys both for commenting!! I really appreciate it !

 

Hamsquatch - lucky for me i'm an EMT, my mom and grandmother are nurses who were 100% anti PM until they met the doctor then they weee 100% for it! as the doctor said "we sit around and wait for the worst thing to happen to you or we get it fixed with a pacemaker and you live a normal life." It's never being reminded of your own mortality so young - I had three experiences in one year I should've been dead and no one knows how i walked away - I just keep saying this pacemaker was meant to give me a new lease!  I hope you are doing well!

 

Robin - Inreplied to your message before I saw your comment hahaha. I'm so sorry to hear that, but it's nice already seeing people who relate! my scar is lower and over more than normal apparently but it's so small and it's healed so nicely i can't complain (especially only 3 weeks just about post-PM!!) It'll be nice talking with you about our adventures !

 

 

thank you both ❤

I'm still coping

by HazeV - 2017-02-14 20:24:40

i was implanted with a PM at the age of 12 and now I'm 23 back then I didn't understand why I had to have this "box" in my chest I just wanted to be normal and not have to explain to people why I couldn't play sports or go on roller coasters . I don't know if anyone else has to carry a magnet with them but explaining that sucked to all through school people wanted to touch my chest or my favorite "so do you have a heart then?"  haha 

over time though it became a part of me weather I wanted it to be or not and today i still  catch my self looking in the mirror moving my arm up and down watching it move inside me. I hate it so much some days cuz in my mind I'm stronger then this condition I don't look like I'm ill but I know it helps me it's That love hate relationship 

please feel free to message me I don't have anyone that has a PM around me and honestly some days o need to talk 

Hard to rationalize

by batesje1 - 2017-04-09 19:57:12

I am an avid runner and love exercising daily. My sister was 30 when she had her PM last July and I was 34 last Halloween when I had mine inserted. Unfortunately we inherited a gene that is unknown for our issues. We were both in 3rd degree heart block when he slept and 2 degree AV block during the day. We both struggle with complete exhaustion which I have been told is normal. Just to give you some hope, today we ran our first 5K today. It was not easy but I nearly cried when I saw her run across the finish line. I know it is going to take a lot of time and dedication but I am willing to do it to feel the freedom I feel when I run. There is an adjustment period but if your doctor says your ok to, you can still be the person you used to be. Word of wisdom, we both had to buy watches to relieve our anxiety so we can visually see that we are OK with our heart rates which is totally worth it and we can now start to trust our hearts again. Good luck I hope this message helps you.

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