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It is a sure thing(surgery)-like you I know my aneurysm isn't going down(4.7)-and it will probably get worse down the road because I am active-you do not still take beta blockers do you? They say Garlic is a mild natural way to lower blood pressure-come in tabs with no odor. I was pretty health conscious-but I will be more so now. It is good to know dacron is like a permanent fix-does the dacron fuse with your natural tissue-I will be seeing my Doc. one more time before surgery.
 
Freddie24

Freddie24

How goes it? My surgery date is creeping up I really want to get it over with--------how are you doing physically-what were the doctors concerns on your follow up appts.? I did some research and the dacron graft get covered in scar tissue--the inside of the graft actually starts to become like a vascular lining.
 
Hi Gary47,

Yeah, I remember how nervous I was, but trust me - it will be MUCH better than you think. Honestly, the worst part of the whole deal is the anticipation and the fear of the unknown. The actual surgery is not that bad. I'm back to 100% and have been for at least a couple months now. To tell you the truth, I felt 100% about 4 weeks afterwards. I was a little tentative with my movements still at that time but physically I felt fine. I know that some members of this site have had much longer recovery periods but I think that's an individual variable that depends more on your physical state beforehand than anything else. What is your surgery date? Are you going to Dr. David?

After I got out of the hospital (5 days after surgery), I had one followup appt about a week later and then one more followup 6 weeks post op. At each appt, they basically just did an echo to make sure that the graft was looking good and that there was no excess fluid buildup (this danger is apparently greater the younger you are due to a younger person's increased immune response). Both appts took about an hour with the echo, consult, etc. After my 6 week appt, the doctor scheduled one more for one year post op. Barring anything unexpected, he said I'd probably switch to check-ups every other year from then on. Apparently, after the 6 week appt, they don't expect much to change so assuming everything looks good 6 weeks post op, you should be very happy with your success. Not to mention that the whole thing will be long behind you at that point.

Good luck as your surgery date approaches. I know that this is a very stressful and nervous time for you but have faith because once you make it through this buildup to surgery, the rest is downhill. I know it sounds backwards but I think most of the members of this site would agree with me that the leadup is the worst part. Have faith and be confident. It will be over before you know it!
 
Surgery

Surgery

Dr. Deeb is going to be my surgeon-he is among a group of surgeons recognised in North America-along with Dr. Daivd-Dr. Cameron-Dr. Vincent Gott etc. in fact I learned their is a world class soccer player who had root reconstructon-and continues to play competively.This I learned from a doctor Zehr,Kenton. Thanks Freddie fo youe reply I am going to get myself a good lazy boy this weekend!
 
Medical Report

Medical Report

The actual dialtion of my aortic root is quite mild----4cm-te ascending aorta is at 4.7cm-----
 
5.4 cm aortic route

5.4 cm aortic route

Hi Gary, I have a condition called Marfan Syndrom which caused my aorta to dialate. I'm 29 years old and over the pats 15 years, my route has dialated to 5.4 cm. My valve was too far damaged to be repaired so I had the "bentol" procedure which replaces the ascending aorta with the dacron fiber and inserts a mechanical valve. Although I am not a runner, prior to last spring when I started noticing drastic decreased stamina, I was training in a martial art (ninjutsu), yoga, working out regularly at the gym, rock climbing, and other vigorous activities. I'm 8 1/2 weeks post-op and unfortunately I've had a number of complications which have hindered my healing. I'm just now getting to the point that I can go a couple of miles on the treadmill at a fast walking pace, I've started back to modified yoga, and starting to practice some of the minor movements of ninjutsu. One thing that you need to be realistic about is the possibility for complications. I truly believed that within a week after surgery I'd be on a treadmill. While it is important to remain positive, it's equally important to be realistic, which I was not. I was basically disabled from my condition since May and unable to remain active, so that was probably a significant factor in my slow recovery. Of course, every person and every case is different, for me I would have preferred to be a little more aware of the possible post-op complications such as arrythmia. I also had an IV site get infected before I was discharged and had to be readmitted the next day as the infection worsened.

I am still being positive and expect to return to training in ninjutsu in February. One thing my cardiologist nurse said to me that helped me to take it one day at a time is "you have to give yourself permission and the time to heal - don't expect more from yourself than your body can handle". Those words have helped me to remain positive. I'll get there...there's no rush... Good Luck to you!
 
Shaz, I am curious as to where you got the name "bentol procedure". Many on this board including myself have a graft and a valve but I have read about everything in print on this procedure and have never heard the term. I checked the internet where you generally get a zillion hits on the subject and got zero. "Bentol Procedure" is not on the internet.
 
Shaz

Shaz

Thanks Shaz-my dialation was due to trauma-one thing I have consistently heard is that dacron repair is durable-----my op. will be valve sparing-but I know this is not a perfect world-took a hatha yoga class this week-to prepare for recovery---I admire the people on this site-I value every correspondence and reply.
 
Marfan's Syndrome

Marfan's Syndrome

Hello Shaz,

My son was diagnosed with Marfan?s Syndrome last year. They?ve decided I also have a much milder case of it. My son has not had the surgery yet, but of course will at some point in the future. His aorta is already slightly dilated.

Did you do the blood test or were you diagnosed from the characteristics? Were you doing annual echos? This is one of my biggest fears... waiting to long to have the surgery done.

Has your cardio said it will be okay for you to go back to rock climbing and other vigorous activities?? My cardio told me Ryan shouldn't be doing them now or in the future. That didn't stop him from taking a rock climbing class in college.

Rain, with a million questions. :)

Oh, my mitral valve was replaced with a St. Jude mechanical valve 4-6-00.
 
Bentol and Marfan

Bentol and Marfan

I'm responding to a couple of posts here...DickV, my surgeon at OSU Medical Center, Dr. David Brown, is the person who told me what the procedure was called. It is also listed in my discharge papers as the procedure that was performed. I may have spelled it incorrectly, but since I am in the middle of moving, I don't have access to the file. I will post at a later date when I verify the spelling.

Rain, I was diagnosed with scoliosis at age 6 or 7. Because of my extreme height for my age and rapid heart rate, the doctors had me see a number of specialists. For years, no one could agree on whether or not I had marfan because 23 years ago, many physicians had never heard of it. My mother was told that I would be dead by the time I was 16. She refused to give up and me to Augusta, GA every six months for two years to slow my rapid growth with hormone treatments. I began beta blockers at the age of 9 and have had annual echo's since then. My cardiologist has always trusted my instincts on my limits and I pretty much have done everything I've wanted to do (except have children). My philosophy has always been that I want to live, not merely exist. So, I take all I can from each day. My cardiologist has cautioned me on my vigorous activities, but also understands my philosophy on life. He is going to release me to start training in my martial art in February and said that I had more restrictions prior to the surgery than I will have once I've completely healed. To me, it's a personal choice...one can let their particular condition control their life or one can truly live life to its fullest. I choose to live and I understand the potential consequences.

As for waiting too long for surgery, if your son is being monitored regularly, they will tell you when he is becoming increasingly at risk for disection. Of course, disection is possible at any stage of dilation, but as the dilation increases, so does the risk. My case was mild for many years as well. But I went from 4.2 to 5.4 cm in less than two years. We are lucky to have been diagnosed early enough. Many people with marfan die during disection without ever knowing they had a problem.

Please let me know if you have more specific questions. I'm not an expert, but I've known that I've had the condition for nearly 23 years. In all that time, I've never met or even spoken to another person with marfan. I hope you'll keep in touch and let me know how it all goes.
 
Thanks, I would like the correct spelling when you have the time. It may help me/others to access information on the web on the valve/graft procedure I have not picked up on before.
 
Hi ****-

Did a search on Google. I came up with Bentall's procedure, or Bentall procedure. There are several items there.
 
Bentall

Bentall

Thanks, Nancy. I wasn't sure of the spelling and my paperwork is burried in a box somewhere. You all are really on top of things here, I like that! I'll definitely be spending time here once my move is complete. I'd like to get to know all of you better and learn of your experiences. Thanks again.
 
Marfan Syndrom

Marfan Syndrom

Hi Rain/Shaz - I too have Marfan syndrome and unfortunately had an aortic dissection while at work. There is a website (Marfan.org) that has great information about Marfan syndrome. I underwent the root replacement surgery in June and am now doing rehab. Somedays I feel better than others. I'm just glad to be alive. Many doctor/nurses do not know what Marfan syndrome is. Many emergency room personnel do not know what Marfan is. When I had my dissection I had to tell them that I had Marfan so they immediately sacnned my heart and thats how they diagnosed the dissection. My 12 year old daughter also has marfans. I will not allow her to participate in any contact sport because if she is hit in the chest it could be deadly. I would definately advise visiting the marfan website. Thay have alot of great information.
 
Marfan's Syndrome

Marfan's Syndrome

Beverly,

Thank you, for providing the web site. My son and I have visited this and many other web sites on Marfan?s. ....he totally understands the risks. He?s 18 years old... and always been very active. He still goes rock climbing, water skiing & snow skiing. Not nearly as often as he used to, but he still goes. I wouldn?t want him to live his life in fear.... just take precautions and be careful.

Thanks again,
Rain
 
Rain

Rain

I kind of lose track of what I say and who I respond to -I am not Marfan-but I am going to undergo a root replacement-my dialation -ascending aorta was due to trauma-I run and workout-my doctors has told me I will be able to start running in 4 mos. and working out with weights again-no more powerlifting-but still some pretty heavy weights (up yo 150lbs) ----I am 47 years old-the doctors gave me the option of using beta-blockers and greatly restricted physical activities I chose the surgery-his name his Michael Deeb out of the University of Mich.
 
Freddie

Freddie

How is it going---still scheduled for surgery Jan. 8th---go in for a final CT on 12-10-01 how are you doing--I want to get this ver with!!!! I e-mailed a pro-soccer player who had similar surgery to us -ti took him a year to completely recover-he is back playing competive soccer--did your blood pressure change after surgery-mine has always been low--how is yours now---take care---keep exercising!
 
Hi Gary47,

Glad to hear you're doing well. After surgery, your blood pressure and heart rate are a little off for a while. They typically put you on a beta blocker for a month or two after surgery just to even everything back out. After that, though, you should be back to normal - where you were before surgery. And before you know it, you'll be back in your normal routine and won't even know you had surgery (except for the scar of course).

Let me know how the ct goes. Just keep the faith because this will all soon be behind you!!
 
Freddie 24

Freddie 24

Surgery is getting close--Jan 28th---my aorta has also started to expand-----my valve will be spared---my arch is OK----I guess their hasn't been a lot of studies on the longevity of a native vavle when it has been spared--I would think as always diet and exercise would be important--How are yo doing??? I will be on by-passfor 90 minutes -surgery total 5 hours--sound familiar-I guess everybody does the "David" technique or something similar-if feasible-my doctor--does the same procedure asToby Cosgrove at the Clevland Clinic-per our discuusssion-he is the most exp. surgeon in Mich. for this type of surgery--and in his words he has been successfull everytime---he says surgery is far less difficult when everybody knows what thy want to do going in.:(
 
My husband had surgery November 6/01. Procedure performed by Dr. Tyrone David in Toronto General was: Aortocoronary Bypass Grafting-x 1, with saphenous vein graft to LAD, Mitral Valve Replacement with St. Jude mechanical Valve, Aortic Valve Replacement with St. Jude mechanical Valve, Myectomy, Recontstruction of lef ventricular outflow tract, Replacement ascending aorta and Patch to left main coronary artery. We are now home and Garry is slow at recovery - he is in constant pain still on heavy duty pain killers, very weak and tired and can do very little - we hope and pray each day that he will get stronger - they have said it will be 6 months before he feels human!!! Lula & Garry
 
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