John Apperson (the author of CadStd) undergoes aortic valve replacement surgery. (As seen through the eyes of his wife, Sherrie Apperson) ----------------------------------------------------------------------- Sunday, July 23, 2000 Dear Family & Friends, I am writing to all of you (many of you for the first time in a long time) to let you know about John's upcoming surgery. Nearly all of our family and friends are "e-mailers", and I thought this would be the easiest way for me to keep you all informed. Don't worry, it won't be the minute-by-minute version, but I will send two or three updates as he recovers so you will know how he is doing. John will be receiving a new aortic valve to replace his worn-out valve on August 2nd. We are very happy with the surgeon, and are expecting John to feel better than he has for years after his recovery. He will be in the hospital for 5-7 days, and then will have a recuperation time of 6-8 weeks. He will not be checking his e-mail for two to three weeks, so if you would like to send him a message, please use this address and I will be sure that he gets it. We believe most sincerely in the power of prayer - it has already given us much comfort and peace, and we know God is watching over us. We also know that there is strength in numbers, so we invite you to join your faith with ours in praying for John, our family, the surgeon and surgical team on August 1st & 2nd. We love you all and appreciate you in our lives. Love, Sherrie Apperson ----------------------------------------------------------------------- Wednesday, August 2, 2000 Dear Family and Friends, Thank you so much for all your prayers! We have felt the strength of them on our behalf, and have been blessed with a calmness, comfort and spiritual peace that I KNOW it was only possible because of your prayers (especially with my active worry gene!). We also appreciate everyone's confidence that things would go well, and the love support you've shown us. John was in surgery from about 8 to 11:30 a.m. today. All went well, and the surgeon was pleased. John got just about everything he wanted (he didn't get his early morning wish to go fishing instead!), but his aorta was good and did not need to be replaced, he got the "freestyle tissue valve" (a specially treated pig valve) he wanted, and he will not have to go on coumadin for the rest of his life (a blood thinning drug he wanted to avoid). After a couple of hours in recovery, he was quite alert but still on a respirator and unable to talk. After communicating several messages through left-handed fingerspelling (not too bad, too hot, take off blankets...), I told him he had gotten the valve he wanted. He fingerspelled "o-i-n-k" and smiled around the respirator tube. That was when we knew he was OK! After they removed the respirator (a painful process John described as, "it felt like giving birth to lungs"), he said that the pounding pulse he has heard in his ears for 20 years is already gone - his heart is already very happy. He hasn't had any chest pain so far, and, more important to him, his brain hasn't felt muddled by drugs. We are VERY happy. John's nurse gave him a "reality check" talk, telling him that he has only crossed the first hurdle and there are many left to go including a long recovery, but we are still VERY happy. He will probably be in intensive care for one more day (they like to keep the "valve jobs" a little longer than the bypasses), and then a couple of days in rehab. Right now, we can only see him for five minutes out of an hour, but that is good because what he needs most right now is to rest and let his medical team do their job. I'm sure I have given too much information for some of you, and not enough for others, but I appreciate your indulgence in my effort to find a happy median. I will probably send the next update on Sunday evening. Again, thank you so much for all your caring support, Love, Sherrie (and John and Melissa and Christie) P.S. There are two types of valves available, tissue (human or animal donor) and mechanical, with several different styles of each. John gave his surgeon his list of preferences, but they couldn't know which one's he was a candidate for until they were actually inside his heart - that's why we had to tell him what type of valve he got. If you would like to know more about his valve, click here:Learn more about the Medtronic Freestyle ------------------------------------------------------------------------- Sunday, August 6, 2000 Dear Family & Friends, John was originally scheduled to be released from the hospital on Monday, but on Saturday they said he could probably go home on Sunday. However, due to lack of good (heart) behavior, his parole has been suspended and he has to wait until Monday anyway - and now it is almost torture because he has been "delayed" a day (one more day of beep, BEEP, poke, stick, blip/blip/blip, BEEP, slam, talk/talk/talk, BEEP, ring/ring/ring...). Actually, it's all my fault - I just asked them on Saturday to assure me that it was OK to take him home with those occasional funny looking heart-beats on his monitor - so after readjusting some of his medication a little, his heart is now beating in time with the right drummer. We are both really glad that he will be READY to come home now, even though he has to spend one more night there (beep/beep/beep). I'm really amazed that bodies can heal well enough after a surgery like that to go home in less than a week, but I guess they know they have to if they want any rest! John really is doing GREAT!!! We are SO happy with his progress, and are sure that he will continue to regain his strength and energy, and will heal well. He started sitting up in a chair and walking the day after surgery, and now is in and out of bed and walking laps with no problems (except pain and the energy to do more ;-). So far, the only down side is that his recovery will take 6-8 weeks, and we just can't hurry that along. We still feel the strength of all your prayers and appreciate how much you all care. John has really enjoyed the e-notes and cards that have been sent. I will probably send my last update next Sunday. Once he is at home and settled, it will just be a matter of waiting for time to pass - no need to share THOSE home movies :-) Thanks again for all your support, Love, Sherrie P.S. What John needs most now is rest, so if you want to, please only call between 6:30 & 7:30 p.m. ------------------------------------------------------------------ Sunday, August 21, 2000 Dear Family & Friends, We were hoping that John could write this last update, but he's not quite up to it yet and we didn't want to wait any longer. Last time I wrote we had only good news, so I guess we should have known to expect something to go wrong. John felt a little less energetic and short of breath on his walks last Tuesday, but we had a check-up scheduled on Wednesday so we waited until then to mention it. Well, it landed John back in the hospital for three days to have about a quart of fluid removed from the sac around his heart. That procedure was uncomfortable, but it relieved his heartbeat and breathing. They said they'd keep him for a little while to continue the drain and to monitor him for infection. He was sent home about noon on Friday, and when we were about half-way home, I reached over to rub his neck and knew he had a fever (101.5). By the time we got the advise we needed and got him back to the hospital (about 6 hours later), the fever was almost gone, but they admitted him for the weekend for IV antibiotics and blood cultures. We got him home again today, and this time I think we'll keep him ;-) He is so "elated" to be home, he's almost afraid he'll jinx himself by being so happy. As of today, he is feeling better than he has since the surgery and is looking forward to the bit of progress each day will bring. We appreciate all the prayers, encouragement and well wishes John has received. They have really lifted his spirits and let him know how much he is cared for. I like what my cousin said about it, "Prayers are so powerful, especially when they are multiplied. Just like the manna from heaven, our prayers must be renewed each day. When someone that normally doesn't come to mind pops into your head, you should pray for that person right then..." We know the Lord has sustained us through this experience, and because of that, we now actually have a list on our wall to remind us of who needs our support through prayer. We are especially mindful right now of our friends who so eagerly gave blood for John's surgery, and found out two days ago that their 3-year-old daughter, Cricket, has a large malignant tumor on her kidney and will have surgery tomorrow. We know that part of our purpose in life is to support and sustain those who are in need, and we will all eventually have such a need. Thank you for filling ours. Love, Sherrie & John Apperson More information about John Apperson Return to the CadStd homepage |