Gary's Journal

My life changed dramatically 6 years ago yesterday: open heart surgery for septal myectomy, mitral valve repair & PFO closure (hole in the heart). Without that surgery I wouldn’t be here today. So grateful to my amazing surgeon & his team! God is good!

Before my weight loss (right) and now (early 2018). Feeling SO much better!

Good evening friends! It's been a while so I thought I'd give a quick update.

My surgery was on August 21, 2015 - some 2½ years ago. Since my last post almost a year ago I've battled - and overcome - some unforeseen medical challenges that seemingly came out of nowhere.

In 2016 I was diagnosed with Stage 3 Chronic Kidney Disease and it continually worsened. In August 2017 I was diagnosed with Stage F3 Liver Fibrosis (NASH). So in October my PCP put me a very specialized diet in order to reverse the liver disease (it's reversible at Stage 3; Stage 4 is Cirrhosis, which is irreversible).

The kidney issues stemmed from repeated heart caths with dye, which damaged my kidneys (my cardiologist has forbidden me from having anymore tests with dyes - a word of caution!). The liver issue was exacerbated by excess weight & a sedentary lifestyle due to my cardiac issues. My PCP also diagnosed me with metabolic syndrome. All in all, last year everything came together in one perfect storm and hit me like a ton of bricks.

So, in October my wife and I accepted the challenge and radically changed my diet under strict doctor supervision. I am happy to report that since early November I have lost an additional 32 lbs (over 50 since surgery). My kidney disease has been reversed and is now normal. My Type 2 Diabetes has been reversed and my A1c is in normal range. I have stopped taking 1 of 2 meds for diabetes. All of the inflammation has gone and my legs and arms look like they did when I was in high school 40 years ago. And, most important, my liver enzymes are better and continue to improve, thus successfully reversing the liver fibrosis. My cholesterol levels have also finally come into normal/acceptable ranges.

My EF is 55-60 (from my last echo in January). My cardiac function is excellent, with only mild leakage, which is in an acceptable range. I can't tell you how much better I feel!

The only issue I'm now facing is ... rib dysfunction and thoracic spinal pain, most likely caused by the rib spreader used during OHS. I started physical therapy today for that, hoping to strengthen the tendons and ligaments in my back damaged by the rib spreader. It seems the weight loss caused the damage to be "revealed" (less fat to cover it up!) and thus cause pain no one has been able to diagnose (until now). This, too, shall pass!

This group has been an incredibly positive experience for me and I am eternally grateful I found it. I am indebted to Adam and his team for all they do on our behalf. I most likely won't be posting anymore, so that others more currently facing their heart valve challenges can share their stories in this space.

But I welcome contact from anyone here who rallied around me during my recovery! Feel free to stay in touch via my personal website - www.garystripling.com.

Love and prayers to you all,
Gary

It's been a while since I last posted. The journey isn't over but it sure has gotten easier. Hopefully this will encourage those of you just starting your journey, or those in the middle of it.

It started with a heart murmur that sounded raspy 7 years ago. That's when I saw a cardiologist for the first time who told me I had Left Ventricular Outflow Tract Obstruction with Systolic Anterior Motion. The nursing students crowded the echocardiogram room because I'm supposedly a textbook rarity. But I survived.

Three years later, in my front yard trimming bushes, I collapsed with complete heart block. Grade 3 they called it. The EMT gave me 3 doses of Atropine to keep me alive on the way to the hospital. That night I was put on an external pacemaker & I received my permanent pacemaker the next afternoon. But I survived.

Three months later an MRI revealed moderate mitral valve regurgitation & hypertrophic cardiomyopathy. My meds were increased. But I survived.

Six months later, after trying to convince myself I would not ever have heart surgery, my cardiologist said the regurgitation was now severe and it was time. But I survived.

In early August 2015 my wife & I met with the cardiovascular surgeon who explained everything & said without the surgery I'd be dead in 2-5 years. We set the date and cried on the 3-hour drive home. But we survived.

On August 21, 2015 my family & I walked into Florida Hospital Orlando at 5am. By 7pm that evening I had endured over 6 hours of open heart surgery, 2 of those clinically dead on the heart/lung machine. They repaired my mitral valve, closed the PFO, & resected a large portion of my septum, including my AV Node, which left me 100% pacemaker dependent (ventricular). But I survived.

Three days later I was back in surgery to repair my pacemaker's atrial lead that had come loose during the heart surgery. But I survived.

Three months later the lead came loose again & the tip was barely touching a nerve running through my chest & stomach. I had weird abdominal pacing. My belly bounced with every heartbeat so the EP turned off the atrial lead. But I survived.

A month later I started cardiac rehab but I could hardly breathe and my heart rate was sporadically racing. I was in AFlutter. I stopped rehab. But I survived.

In early December I had cardioversion that put me in sinus rhythm for 3 weeks so I could get through Christmas and I survived.

On New Years Eve 2015 I was back in the hospital to have the atrial lead replaced once again and during pre-op they discovered I was in AFib. So I had atrial ablation plus the lead replacement surgery. I watched the fireworks from my hospital room that night. But I survived.

In February 2016 I resumed cardiac rehab & had completed all 36 sessions by late April.

I survived the heart surgeries which led to debilitating pump head, horrible depression, caused me to develop Stage 3 Chronic Kidney Disease, significant Vestibular Dysfunction, and now I battle mild pulmonary restriction. At 58 years old.

My story is not unique. But like you all I survived. We survived. And life has meaning and purpose which we seek to fulfill. Don't ever let anyone diminish what you've gone through - or are going through now.

Because you - and I - survived what most people will never experience & cannot understand. And we have the battle scars to prove it.

I'm kinda freaking out right now. I had OHS (full sternotomy) for MVR, septal resection for cardiomyopathy and PFO closure on 08/21/15. I'm also 100% pacemaker dependent.

Lately I've had shortness of breath, chest tightness, fatigue - the symptoms I had prior to surgery. Today I saw my cardiologist and he thinks it could be diastolic heart failure from a stiff heart. My right atrial pressure is elevated and I'm carrying fluid. So I had an echocardiogram today and had labs drawn this morning.

After the echo the Tech would only say my gradient is a little higher than my last echo 3 months ago. Not sure what that means. My cardiologist started Lasix & potassium today for 3 days. I also have Stage 3 Chronic Kidney Disease, so they're watching how the Lasix and potassium affects my kidneys as well.

I'm supposed to travel from the US to Eastern Europe in a month on business and I'm very nervous now about this trip, not to mention the prognosis possibilities. I meet with the doc on Tuesday to review the test results. Your thoughts and prayers are appreciated once again.

Just a quick update: had my 3-month follow-up today (I'm on an every 3-month cardiac follow-up since OHS on 08/21/15). The only concern my cardiologist has is that I'm retaining fluid, most likely due to the Stage 3 Chronic Kidney Disease. So he, my nephrologist and endocrinologist are coordinating efforts to keep my kidneys functioning by prescribing the right meds. As he told me, "you don't die from fluid retention, but you can die from kidney failure."

He increased my Coreg from the minimum of 3.125mg/2X daily to 6.25mg/2X daily to "keep my heart function stable" even tho I have a strong heart. Does this make sense to anyone?

I'll have an echo in 6 months to check the mitral valve repair, septum resection and gradient.

I did ask about the wires I am feeling in one particular spot (top right of the septum). He advised against doing anything unless I just couldn't live with it anymore. He said it's very invasive and my cardiovascular surgeon (in another city) would be the only one who would tackle removing them. So they're staying put!

Overall, he was pleased with my recovery and I'll see him again in 3 months as they monitor my kidneys. Interesting how one med for one condition affects so many others!

Hello friends. It's been a while since I posted. Life has a way of resuming, whether we want it to or not.

My last heart surgery (after the "big" surgery on August 21, 2015) was on New Year's Eve 2015. I completed my 36 sessions of cardiac rehab last April. I began rebuilding my business clientele (I took 6 months off work since I'm self-employed) and started traveling again as a consultant.

Ever since the OHS on 08/21/15 I have experienced ongoing dizziness, headache, lightheadedness, balance challenges, and on some occasions near-syncope (almost fainting). I kept thinking this would eventually subside and go away as I recovered from the OHS. It never did.

This past August I had a bad case of vertigo which lasted about 10 days. I've had vertigo over the years, but usually for only 1-2 days at the most. This episode was really bad.

In September I finally was referred to a neurologist after my cardiologist completed a full work-up and declared me free of any cardiological issues. The MV repair surgery was a success, recovery pretty much complete, and rehab extremely valuable. Other than sternum aches every now and then, I've felt great. Now if I could just get rid of this dizziness & headache!

The neurologist had me do a balance test in his office, as well as ordered a CT Scan. I failed the balance test and the CT Scan came back negative.

So, in late November I was diagnosed with significant Vestibular Dysfunction Disorder. Now my headaches, dizziness, and feeling light-headed had a name. I began Vestibular Rehab Balance Therapy (VRT) in early December twice weekly.

Today, I had my 1-month re-evaluation and I have improved significantly! No more vertigo. Headaches are fewer, dizziness is better and I'm not light-headed as much. I just have to learn how to adjust to my surroundings. If you visit http://vestibular.org you can read all about it.

What has this to do with my heart valve surgery? My neurologist and balance therapist both believe the significant time under anesthesia and the invasive nature of open heart surgery caused my vestibular dysfunction. And it wasn't going away on its on.

So I encourage everyone not to ignore symptoms you think may or may not be a direct result of your surgery. So much is done to us while we're on the heart/lung machine, during the surgery, etc. that sometimes it takes a while for the cause & effect of certain symptoms to manifest.

I have 4 weeks of balance therapy left and have exercises I work on daily. Dizziness and imbalance issues for open heart surgery patients is real and there is help for it!

Happy New Years everyone - it's going to be a great year!

As I posted earlier, I started having symptoms similar to those I had before OHS (fatigue, shortness of breath, slight swelling in ankles). I had an echocardiogram yesterday (9/19) and today met with my cardiologist.

Good news! My EF is 60-65%. The MVR is holding nicely and my heart is doing great! Seems I have a bit of "stiff heart" - diastolic dysfunction (see http://www.healthcentral.com/heart-disease/ask-doctor-44701-70.html for info). I'm also anemic due to Stage 3 Chronic Kidney Disease (recent diagnosis) and started on iron last week.

But overall, I have no limitations on exercise, so it's back to the gym for me so I can continue to lose weight (I've gained back about 5 of the 24 lbs I lost after OHS last year). What a relief to know my heart is functioning as it should and no more valve issues. Thanks for the thoughts and prayers!

As I posted earlier, I started having symptoms similar to those I had before OHS (fatigue, shortness of breath, slight swelling in ankles). I had an echocardiogram yesterday (9/19) and today met with my cardiologist.

Good news! My EF is 60-65%. The MVR is holding nicely and my heart is doing great! Seems I have a bit of "stiff heart" - diastolic dysfunction (see http://www.healthcentral.com/heart-disease/ask-doctor-44701-70.html for info). I'm also anemic due to Stage 3 Chronic Kidney Disease (recent diagnosis) and started on iron last week.

But overall, I have no limitations on exercise, so it's back to the gym for me so I can continue to lose weight (I've gained back about 5 of the 24 lbs I lost after OHS last year). What a relief to know my heart is functioning as it should and no more valve issues. Thanks for the thoughts and prayers!

As I posted earlier, I started having symptoms similar to those I had before OHS (fatigue, shortness of breath, slight swelling in ankles). I had an echocardiogram yesterday (9/19) and today met with my cardiologist.

Good news! My EF is 60-65%. The MVR is holding nicely and my heart is doing great! Seems I have a bit of "stiff heart" - diastolic dysfunction (see http://www.healthcentral.com/heart-disease/ask-doctor-44701-70.html for info). I'm also anemic due to Stage 3 Chronic Kidney Disease (recent diagnosis) and started on iron last week.

But overall, I have no limitations on exercise, so it's back to the gym for me so I can continue to lose weight (I've gained back about 5 of the 24 lbs I lost after OHS last year). What a relief to know my heart is functioning as it should and no more valve issues. Thanks for the thoughts and prayers!

My cardiologist has me scheduled for an "unscheduled" echocardiogram on Monday & he wants to see me on Tuesday. I'm having shortness of breath, no energy & tightness in my chest. Praying the "slight" aortic regurgitation he detected earlier this year hasn't progressed. The thought of another OHS terrifies me. Hopefully it's just a medication adjustment.

My One-Year OHS Anniversary was on 8/21 - about 3 weeks ago. So today, at the urging of my son, I joined a gym! I had already completed 36 weeks of cardiac rehab in April, but really wanted to continue moving forward with my recovery.

Plus, today my endocrinologist told me I'm anemic, probably due to the "acute renal episode" I recently had (laser lithotripsy for kidney stones - I'm at Stage 3a Chronic Kidney Failure), as well as the ongoing recovery from everything cardiac-related. No wonder I'm so tired all the time!

Since I'm 100% PM dependent, my cardiologist set my heart rate goal of 120 on the treadmill. I got to 110 today! For anyone 1 year or more post-OHS, what exercise heart rate have you been told to shoot for?

Eight days ago, on August 21, 2016, I celebrated One Year of Survival from Open Heart Surgery (yes, I'm a little late on this post)! The road to recovery is a long, arduous journey but with the support, love and help from my family and amazing medical team - and the encouragement and support from this community - I have made that journey successfully.

I can't thank enough my Jacksonville, FL-based cardiologist Dr. Sumant Lamba, my Orlando-based cardiovascular surgeon Dr. Tom Martin and the wonderful healthcare professionals at Jacksonville Clinic & First Coast Cardiovascular Institute, Florida Hospital Orlando (for the BIG surgery), and Jacksonville, FL hospitals Memorial Heart Center, St. Vincent's Medical Center Riverside and Orange Park Medical Center (between the post-surgery testing, cardioversion, atrial ablation, & pacemaker surgeries, I got to spend time at all these wonderful facilities!).

I was so blessed that my family (children, sisters & dad) made the trip to Orlando to be with us during the week of my surgery. It was such a blessing that my wife's best friend from high school offered the use of their 3-bedroom vacation condo in Disney Village for 10 days free of charge! Everybody had someplace to sleep and it was a ground-floor handicapped unit, which was so cool since we stayed there for 2 days after I was discharged from the hospital before driving home to Jax.

The biggest blessing in my life - after my relationship with Jesus - is that my wife and children have been so supportive and diligent in their care for me during my recovery. It's been an adventurous year - one I don't want to repeat - but I'm looking forward to many years to come in better cardiac health than I've been in the past 6 years!

I'm still recovering mentally & emotionally, as well as dealing now with kidney issues brought about in large part from the damage caused by the contrast dyes used in numerous heart caths. Word to the wise - if you're diabetic be sure to limit the number of heart catherizations with contrast (dye) your cardiologist orders. It WILL damage your kidneys. If you have to have one, check with your nephrologist first so he/she can prep you with lots of fluids to flush out the dye and not damage the kidneys.

I can't believe how much better I feel and can do now that my ticker is fixed! Instead of 5-6 years left I have a normal life-expectancy. And that, my friends, makes it all worth it!

As I approach the 1-year anniversary of my open heart surgery for MVR, PFO closure & septal resection I had on 8/21/15, I want to encourage those facing OHS or any kind of heart surgery to document your experience with photos & journaling.

The surgery is a major part of the experience but it's not the entire journey. I wish I had pics of those first few weeks after surgery. Fortunately my wife has a great memory & doesn't mind recounting to me what she & the family went thru while I was in surgery - clinically dead while on the H/L machine for 2 of those 6 hours.

I recommend an app called Day One for personal journaling. In addition, I posted regularly for 6 or so months in my profile here.

Recovery is a process. For some it's shorter than others. But the journey changes us forever & documenting it is both therapeutic & informative for our loved ones.

Prayers & best wishes for those about to take the next step with OHS & those already on your journey!

Just 2 days short of 10 months since OHS (mitral valve repair, PFO closure & septal resection) and ... I mowed the lawn today! It was both refreshing (beautiful windy Florida day) and tiring. The last time I did yard work I collapsed in the front yard with complete heart block. But thanks to my amazing cardiologists & 36 sessions of cardiac rehab I feel like a bionic man (well almost). Hurray for a small accomplishment today!

Celebrating 9 Months Post OHS (08/21/15). I think it's healing pretty nicely, although I'm still looking for my beach bod somewhere in there.

Yesterday - 9 months post OHS - I had an endoscopy. Since the surgery last August my IBS has gotten worse and my hiatal hernia really aches.

After my wife got me home my chest starting hurting, was tight, and I had abdominal pain. I called the doctor who performed the endoscopy and he said it was probably spasms from the biopsies he took of the lining inside my stomach. Man, did that hurt!

Today I've felt much better - almost "normal" (whatever that is). Here's my question: is it possible to exacerbate a hiatal hernia when you have a full sternotomy? The endo didn't show any problems there, except noting "a 1cm hiatus hernia present."

Nine months ago today - 8/21/15 - my family and I walked into Florida Hospital Orlando at 5:30 AM for my OHS. After six hours of surgery I was in recovery that evening, having had a mitral valve repair (with a 30mm annuloplasty), septal resection and PFO closure. During the surgery my pacemaker's atrial lead came dislodged, so 3 days later I was back in surgery for that.

It's so hard to describe what the past 9 months has been like, as well as how going thru something like this changes you in so many ways - things the healthcare pros don't tell you about. Most of you reading this will know what I'm talking about.

I'm so grateful for the superb care I have received from my doctors, nurses, rehab folks, etc. these past 9 months. I'm stronger now than I have been in years. God is faithful and He is my Healer!

I'm 9 mos. post-OHS. Recovery has been slow but steady. Completed rehab 3 weeks ago. Good report from cardiologist yesterday (see yesterday's post). However, lately I've been depressed & feeling like I'm on the edge of losing it. Today I had an emotional mini-meltdown. I'm an otherwise happily married man with grown children. Any other guys experience this? Should I tell my cardiologist?

Hello friends. Had a follow-up with my cardiologist today to review my latest echo. My EF is 60-65% with some mild regurgitation across all my valves, especially the aortic valve. That will be monitored with 2X-year echocardiograms. My pacer is ticking along at 100% dependent and I'm still in sinus. He started me back on the Losartan since I'm diabetic. I'm almost 9 months post-OHS and doing so well I don't have to see him again for 6 months - HURRAH!

Last day of cardiac rehab. I finished all 36 sessions - finally!

Finished up cardiac rehab today - 36 sessions since last October (with a long break for cardioversion, atrial ablation & atrial lead replacement surgery). Can't believe how much better I feel. Thankful for the nurses who monitored me & encouraged me to push through. Gonna be a great summer!

Eight months ago today - 08/21/15 - my wife, 2 children, and sisters walked into Florida Hospital Orlando at 5:30 AM not sure what the day would hold. After over 6 hours of open heart surgery I woke up with a repaired mitral valve, a resected septum, a PFO closure & 100% pacemaker dependent. In the following months I went into AFlutter, had cardioversion, went into AFib, then had atrial ablation and atrial pacemaker lead replacement surgery on New Year's Eve. Since then I've been in sinus rhythm and feeling better by the week!

As I'm in the music industry, a new Danny Gokey song "Tell Your Heart to Beat Again" so speaks to me as I have fought & survived this literal heart battle. I am slowly but surely getting stronger each day as I work back into a routine of serving others thru my agency. I still have pain & weakness I never imagined but I have only 2 more cardiac rehab sessions (out of 36), which has helped so much!

Thanks be to God for what He has brought us through! Enjoy this song from me to you.

http://youtu.be/azYK8I2uoog

I'm 7 1/2 months post-OHS for MV repair, PFO closure and septal resection. I'm 100% pacemaker dependent. I should complete cardiac rehab in 2 weeks (delayed because of PM and AFib issues last fall). Question: I'm having a hard time staying on task and get easily overwhelmed juggling everything, whereas before surgery I did just fine. I'm 57 yrs old and own my business as a consultant in the music industry (travel 1-2 weekends/month, lots of details to manage). Short-term memory issues are worse now, too. Will this all get better or is this the new normal? My wife said to ask you guys. Comments?

I had my follow-up echocardiogram last Monday - 7 months/7 days since OHS - and the test results are so good I don't have to see my cardiologist for another 6 weeks! Hurrah!

The 6-8 months prior to the 8/21/15 surgery were so bad I could barely function. Now I'm beginning to remember what it was like to feel "normal" before things went downhill. I have 8 more rehab sessions and I'm done with that as well! I can't stress enough how important the rehab is for a successful recovery.

I'm pushing 6+ hour work days now (I'm self-employed and work from home). Muscle soreness is not as bad but I still struggle with fatigue and some emotional ups and downs. But overall, I can't get over how much better I feel.

To all of you facing OHS, know that it DOES get better. Open Heart Surgery is NOT for wimps!

With my beautiful wife at 5:41 AM, August 21, 2015. Ready for OHS that wouldn't start for another 5 hours.

Almost finished with 36 weeks of cardiac rehab!

My first (and only) mirror selfie. Taken at rehab 3/9/16 - first day working with weights (3 lbs)!

Since my open heart surgery last August, I'm now 100% pacemaker dependent. When I first received the pacemaker in October 2014 my heart was contributing between 40-60%. Now the pacemaker does all the work, thanks to the septal resection during the OHS.

It's very sobering to realize that I'm dependent on a little device in my chest to keep me alive 24/7. Sometimes during the day, and especially at night, it hits me like a ton of bricks and my mortality sucker-punches me in the gut. At 57 years old I didn't expect to have to deal with something as life-altering as this.

But, after the 6-hour OHS last year (and subsequent cardioversion followed by an atrial ablation and 2 atrial lead replacement surgeries), nothing seems too insurmountable anymore on the one hand. Yet on the other hand I feel very vulnerable, even with a normal life expectancy.

I thank God every day for each heartbeat He allows me to have and every breath I can take. Does anyone else think about such life and death issues after OHS? Or have I become to introspective in my old age - LOL!?

Six 1/2 months post OHS!

I'm a little over 6 months post-OHS. And my last pacemaker surgery was on New Year's Eve (I've had 2 pacemaker lead repairs since OHS in August). For the most part I've started feeling normal again. But I was in such bad shape prior to surgery I've almost forgotten what "normal" feels like.

Today, however, I'm exhausted. Mentally hitting a wall this week, forgetting things I should remember. My wife reminded me today the cardiologist told me last month I was moving too fast and needed to slow down. Guess it caught up with me.

Even having a simple business consultation yesterday with clients (yes, it was 6 hours in a conference room) wore me out. And this afternoon through the evening I've had to rest. Five minutes at the computer, answer a few emails, then rest for an hour. Then repeat. My mind has so much it wants to do but my body isn't cooperating.

At this point should I be further along in my recovery and have more energy and stamina? I know everyone is different. Guess I'm just weary of the fatigue, muscle aches, back pain, and sternum tenderness. And dealing with a bit of depression, which I didn't expect this far out. Thanks for letting me share here. Love this group!

Six months ago today, on August 21, 2015 I had open heart surgery (MV repair, septal resection & PFO closure). It was life-saving and life-changing. Today I'm celebrating my 6-month anniversary of LIFE and I couldn't have made it this far without the incredible support, love, and care of my bride of 35 years.

It's amazing to think that 6 months ago today Laura, our two children, my sisters and I walked into Florida Hospital Orlando at 5:30 AM, unsure of what the day would hold. My dad even drove all night following a family funeral to be with me the day after surgery. Seeing him standing in my hospital room doorway early Sunday morning brought tears to my eyes. Six days later I walked out of the hospital (with a lot of help!) a changed man.

The healing process has been rough at times, with some complications and hurdles, but today I feel so much better than I have in 5 years. And I'm not even half-way finished with my cardiac rehab! Special thanks to my amazing cardiologist Dr. Sumant Lamba (Jacksonville) and my surgeon Dr. Tom Martin (Orlando) for their expert care. Most importantly, however, is my gratitude and thankfulness to God my Healer and Life Sustainer. Looking forward to many more productive years ahead!

Celebrating 6 Months Post-OHS!

5½ months post OHS

I saw my cardiologist this morning for my monthly follow-up (my OHS was on 8/21/15). All is well. But because of the chest and back pain my cardiologist thinks I have costochondritis. My sternum aches and every muscle, tendon and nerve in my chest and upper back is still reeling from the 6-hour open heart surgery, the 2-hour pacemaker surgery, the 1-hour cardioversion, and the 2-hour New Year’s Eve surgery and ablation procedure. I’m done with hospitals!

So, my awesome cardiologist has advised me to slow down a little. My mind says “hey, I’m all better” but my body says “hey, you survived open heart surgery but you’re still healing.” He is concerned I’m overdoing it, so I’m reluctantly trying to relax more and slow down. Easier said than done!

Today I finally was able to resume cardiac rehab. I had only completed 10 sessions when I started having the Aflutter issues back in November. After cardioversion in early December (which held only for about 3 weeks), atrial ablation, and pacemaker atrial lead replacement surgery on New Year's Eve, I really was anxious to get started again. Today was 30 days since the last surgery so I was very excited to get back to rehab this morning!

The funny thing is that when I got hooked up to the heart monitor at rehab, the nurses all said they couldn't find my atrial pacing (I'm 100% PM dependent). No P-waves either. So I texted my cardiologist, who arranged for me to have a PM interrogation this afternoon.

Fortunately the nurses missed it somehow and I'm in perfect sinus rhythm! And my P-waves are at 4.9 (out of 5). I'm looking forward to celebrating my 6-month post-OHS anniversary on 2/21. Oh, and our house sold so we're moving this month. So all is well in a busy new year!

This past Thursday was my 5-month post-OHS anniversary. I do believe the New Year's Eve atrial ablation and pacemaker lead replacement surgery was successful - I still feel so much better! I am experiencing collarbone & upper back discomfort. Some of the pain is from the annoying pacemaker incision. Seems something muscular is always aching. So I'm returning to cardiac rehab tomorrow (Monday). I completed only 10 of 32 sessions when I went into AFL back in late November. Looking forward to getting back on the bicycle and treadmill and getting my energy level back up!

Tomorrow will be 5 months post OHS - yahoo! I had cardioversion in December and atrial ablation & pacemaker lead replacement on New Year's Eve. Now my question: I'm having intense back pain between my shoulder blades. It's a burning pain. My upper chest/clavicle area is sore, as to be expected, but the upper back pain is awful. Is this a normal after-effect from all I've had or do I need to see a chiropractor? Any thoughts?

Had a good report today at my cardiologist's office! The staples were pulled from my New Years Eve pacemaker surgery & the leads are firmly in place and firing correctly. The atrial ablation procedure seems to have worked (I'm still in sinus rhythm). I get to resume cardiac rehab next week. Pacemaker-assisted cardiac function is very good & I don't have to see a doc for 30 days! Yahoo!

Now that I'm on the other side of OHS, pacemaker surgery, cardioversion, ablation, etc. (whew!) I need to get a medical ID bracelet, mainly because I travel alone quite frequently for my business. Anybody have any suggestions on a provider you would recommend?

Pacemaker incision, entry #3 from 12/31/15. Staples coming out on Monday!

OHS scar at 4 1/2 months.

I'm one week post-RF Ablation. Still having tightness and burning in my chest and some upper back pain on my left side, along with tiredness. Anybody know how long these symptoms should last?

I checked into the hospital on New Year's Eve for a pacemaker atrial lead replacement & the EKG revealed I was back in AFib (I was cardioverted 3 weeks ago and I'm 4½ months post-OHS). So I had an atrial ablation right before my "little zipper" was reopened (for a 3rd time) for the atrial PM lead replacement.

Finally was able to get a shower today and, when my wife removed my pacemaker incision dressing, I cringed when I saw the 9 staples (2 previous entries here were closed using steri-strips). Yesterday when the nurse was preparing me for hospital discharge she had to remove about 12 staples from my groin (entry point for the atrial ablation). The frickin' doctor put them in cross-hatch (half on top of the others) and I thought I was going to die when the nurse started pulling them out. Even my wonderful nurse was PO'd at how the doc put them in. I'm not a screamer - but that changed yesterday. Hoping the pacemaker incision staple-removal won't be as painful in a week!

My pacemaker site is very sore & I'm in a sling, but my heart is once again in sinus rhythm & both PM leads are firing. Here's to a healthy, 100% battery-operated new year!

I think someone has mentioned this, but I can't recall where. Since my August OHS for MVRepair, I've developed a heart beating sensation in my right ear. I have a 30mm annuloplasty ring. Is this beating normal? Will it go away? Any medical explanation for this? Thanks!

Happy to report that the cardioversion I had last Wednesday has held and I'm still in sinus. Met with the electrophysiologist today and the next step is to replace the atrial lead to my pacemaker (it's been "dead" since becoming dislodged somehow in the past 6 weeks). Looks like a New Years Eve surgery is on the calendar!

TEE/Cardioversion went well today! No pain & no memory of the procedure. And I'm back in sinus rhythm! Thanks for the kind words & prayers.

I'm having a TEE/Cardioversion on Wednesday to put me back in sinus rhythm since I have A-Flutter. After 6 hours of OHS in August I know I've gone thru the worst. But when they tweak my pacemaker I always feel like I'm about to hit the floor (I'm 100% PM dependent). So, the questions are: will I feel the shock and will it wake me from sedation? Any pain afterwards? I'm a scaredy cat when it comes to electrical heart stuff, so thanks for any comforting words.

I'm 3 months post-OHS for MVR. Full sternotomy. I've developed a really uncomfortable soreness in my chest on both sides of the incision. Even hurts to take a deep breath now. It had gotten a lot better but now I feel as sore as 1 month post. Is this normal?

My OHS for MVR was on 8/21/15 . My electrophysiologist confirmed today I have developed A-Flutter. This is primarily due to the "wear & tear" on the atria pre-surgery from the MR. I went from moderate to severe MR in 7 months.

His recommended course of action is a diagnostic TEE and while I'm under go ahead with cardioversion. He wants to see first the condition of my atria septum (?) before the cardioversion to determine if ablation would work better.

Can I get some feedback on cardioversion? Good results or bad? Any recovery period?

Thanks!