As many of you know I was born with congenital heart defect and had surgery at age 3 to repair the valves in my heart. Since the surgery I have lived a mostly normal life and have remained active. I see my cardiologist every few years and he has always been very encouraging about my progress. Last time I went, he said I was doing wonderful and that I did not need to come back for four years. This was very encouraging to me and my family.
Early this summer I went for my check up. I was expecting an easy routine check up because last time we got such great news. My doctor said that my heart is still functioning the same as it always has, but it is working very hard and I will get worse before I get better. He then said that I might need a valve replacement in the next few years to help my heart work its best.
My cardiologist then called me a few weeks latter and asked that I meet with the other doctos sooner than planned because I need the surgery THIS SUMMER. This was difficult news to hear, but my friends and family were very supporative and encouraging.
I saw the surgeon Friday. He was very nice and explained all about how the heart works and the process of the valve replacement. He then answered all my questions and made us feel very comfortable. He explained that I would be up and out of bed the first few days. He said that the recovery would be easier than we expected, but should plan not to be back at work full time for about two months. We were able to schedule the surgery for Wednesday, August 6th at Medical City of Dallas.
I also met with a arrhythmia specialist because my cardiologist explained that my heart rhythms are irregular. The Dr. explained how my heart was working and the valve and rhythm problems it was having. He started telling me about the options and started with the worst and moved to the best. Basically, the valve operation should take care of the problems, but I might need a pacemaker or maybe even a defilibalater (sp?). The irregular rhythms are not a big problem now but they could be if we don't take care of it. I will need to go back and see him a month after the surgery to see if I need anything else. He said it is very possible that I may need a pacemaker somewhere down the road if not now.
In about 6 months I hope to feel so much better than I ever have.
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"I have set the LORD always before me. Because He is at my right hand and I will not be shaken. Therefore my heart is glad and my tounge rejoices; my body will also rest secure." Psalms 16:8-9
4 comments:
Wow! To feel "better than ever". To me you are such a ball of fire, if they give you a pace maker, I must insist that it comes with a remote controll! I love you and will continue to pray for a successfull surgery and speedy recovery!
Lindsey, I am praying for you. My mother is having her aorta valve replaced on Monday at Medical City so I will be there all week. If you need anything let me know. My mother's name is Ruth Innes. My cell is 214 405 3272
Love, Lynda
Hope everything turns out great for you! I got your site from Brooke and Freeland. I will be praying for you!
I love your blog....and will enjoy being connected to heart to heart! We will be there....you and your family have been in our prayers. Sending heart hugs....love you so much, Becky and Jim
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