Slow transit constipation and surgery
Hi, I have slow transit constipation and Ive tried everything with little help. Amitiza, linzess, trulance...diet modification, pelvic floor therapy...etc. It affects the quality of my life every day. It started at 18 and im almost 34. I cannot maintain a job or even finish school. Just saw a new gastro and he wants me to "drag my feet" on surgery. I know it is not to be taken lightly but i want a life, while im rather young. Just really stressed and would like any thoughts or info that would help. Thanks.
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Yes because I had acdf 3 fusion surgery when this happened but we can’t seen to connect them.
Hi, again, @mothermary1 I understand that you are very conflicted about the upcoming surgery. Remember,that everyone on Connect is solidly behind you. We’re going to virtually hold your hand for the next several months!
When i worked as a nurse, i frequently took care of patients who had had major abdominal surgery. Yes, it was tough, but in a good hospital with good nurses, its very doable. The 1st 24 hours are the hardest because lots of people are coming and going. Every day gets a little better. Pain control is taken very seriously, too.
Turn toward the future now and plan what you will do while you’re recuperating. Paint? Knit? Read? Play games? Will you be going to a big hospital?
It's awful that you've been through so much. I just heard back from one of my physicians who had shipped me off to another specialist. He wants to order an ultrasound of the diaphragm and look into vagus and phrenic nerve more closely. I had just decided to throw in the towel and try and figure out my stuff on my own.
Yes, I do agree that drinking too much water is not recommended, one may even die from it when electrolytes are too deluded or non-existed, and it almost happened to me as well. Joanne, you've been in this situation a long time, and I'm sure that you did all the homework about what's good, what's not. What I've learned the hard way is that we all should look for natural remedies, not chemicals which may cure one problem, and cause many new problems. We all are part of nature, we do self heal, to certain extend off course, that's why it's important to try everything there is before going under the knife. That was my mistake, and I'm still paying the price for it, for trusting the surgeon too much just because he had thousands of similar surgeries under his belt.
Take care Joanne.......Jerzy
Hi Jerzy, I’m still going to PT which is internal and external. I take no pain drugs as I’m allergic to everyone of them. I’m going to weekly acupuncture too. I just after 14 months see no results. If I saw a slight change believe me I would be thrilled. I’ve been told the colon is a very stupid organ,tough to get going.
After acdf fusion surgery in Boston I followed up with a gag reflux study.if I remember correctly that was at 6 month follow up. Also during my surgery he was assisted by a nerve specialist and I don’t know her professional name. She was in the operating room doing a similar function to acupuncture but more in depth. She stimulated many nerves during the entire surgery. I woke up when fully alert and many little pinhole size bruises everywhere, I had them in my head as well. Prior to surgery I was explained her role and how it played with having a large fusion. I had a lot of concern ending up with nerve damage. I’m quite sure I still could have.
My date is set. I’m following through with PT and acupuncture till very end with hopes it may jump start my system.
I just feel I’ve done all the non medical drug related types of care offered to me. Maybe I’m missing something I’m not aware of. Can you share more of what you sent through after surgery and what you still are going through. Also, I’m guessing and just a guess you went to a large NY hospital. Did you use a large well know facility. Having had many surgeries I surely believe it’s better. Be well and happy, Joanne
Hello Becky, yes it will be done at Mass General Brigham & Womens in Boston. They are affiliated now . I’m feeling better about it and if you have seen my posts, I continue with PT and acupuncture hoping for a miracle. It’s mostly fear of the unknown like most surgeries. I’m coming to peace with it. Many thanks, Joanne
Hi, Joanne, you’re sound better every day! I think you’ve taken charge and won’t let this surgery beat you! Another question: do all of the doctors/surgeons know about your allergies to pain meds? What do they plan for pain relief?
Becky, my past surgeries I have received nothing, ever. The acdf 3 fusion was by far the worst. I’ve had many and everything they have tried gives me rapid heart rate, vomiting sometimes a rash. At pre-op we will have a discussion and see for this surgery are their options. I had a bunion removed and a plate put in my foot about 5 years ago. I thought recovery was just terrible. I needed my other foot done but declined.
Then last year my neck. Three months of a hard brace 24/7 and no pain med. it was tough. I don’t ever seem to get offered options other than I’ve pump or an injection. I always ask. I have no idea the what discomfort I will have. I had my gallbladder removed years ago and I felt the gas pain was awful but the more I walked the better I felt. I’m thinking walking right away if allowed is key.do you know of anything I can suggest. Thanks for keeping up with me. I’m hanging in…Joanne
I have chronic constipation to the point of ridiculousness. I had an anal mamentry test and biofeedback was suggested. Can you explain what it entails? I also have autonomic small fiber neuropathy which causes this. I have always been constipated but this is on a whole different level. I am scheduled for the smart pill to see if it is a motility issue. What surgery are you holding off on?
Hi, @mothermary1 Joanne. Just checking to see how you’re doing. I hope you’re doing ok and keeping your spirits up. When is the surgery scheduled for?