Posted 2/14/2016 10:32 PM (GMT 0)
New to this forum. Thrilled to see so many people with similar experiences and stories to share. I was recently diagnosed with a giant paraesophageal hernia, with most of my stomach in my chest. I'm also severely anemic (but didn't know it until recently), asthmatic and have years of GERD experience as well. I should have taken out stock in Pepcid and omeprazole years ago.
For the past couple of years, I've been plagued by exhaustion, shortness of breath, racing heartbeat upon exertion, headaches and the feeling that I simply couldn't keep up like before. In my early 40's and, although slightly overweight, not obese, I was baffled by my inability to do the things I love to do. I've always been active outdoors and a super on-the-go kind of gal. And, of course, the more I limited by activities, the more weight I gained. I thought that everything I was feeling was due to my increased weight and, perhaps, asthma issues. But it didn't make sense as friends who were also asthmatic and far heavier than I could do ten times more and not be winded and exhausted.
During a chest X-ray for a bout of bronchitis, my results showed a "large hernia." Thankfully, my doctor sent me for a surgery consult. Turns out, after an upper GI, endoscopy, manometry and ph probe, that I had more going on in my body than I thought. My surgeon links all of my difficulties to the giant hernia. He believes:
- The anemia is caused by the hernia. The anemia causes the exhaustion, heart racing and shortness of breath. The hernia, too, can cause these issues as the stomach is taking up space in the chest.
- The GERD is at least strongly exacerbated, if not caused by, the hernia. With my stomach in the wrong spot and upside down, reflux is common and frequent. Reflux can also exacerbate breathing issues, particularly for asthmatics whose lungs can be irritated by the aspiration of stomach acid.
Who knew that all of these things -- these annoying, life-altering things -- could be connected? After years of feeling a sense of unexplainable physical deterioration, I now have hope. I am scheduled for surgery in a couple of weeks to repair the giant PEH along with a full Nissan fundoplication wrap. I'm nervous about the procedure and the possible side effects (post-op pain, swallowing issues, inability to burp/belch, inability to vomit, if needed, etc.) but excited by the possibility of having my physically active life back. I'd love to be able to walk, hike and more without feeling horrible.
Would love to hear from any of you with similar experiences, particularly your post-op successes and challenges. I'm sure I'll be posting more soon as questions pop into my head. Thanks to you all for being here!