Cervical Rib Surgery Experience
Jun 8, 2015
After a long two years trying to get a Consultant to help me. Yes I found the right one. Mr Fox a vascular surgeon. I saw him on 22nd May 2015. He diagnosed me with two extra ribs "one each side" . And Said he would operate on my left side first, has this was the worst side "pulse was very weak when arm was raised. Had my op on Thursday 4th June 2015. Mr Fox removed my first rib and some muscle. Op started at 10,30 and in recovery room by 2.o'clock. Rib was removed from the front just above collarbone and had draining tube, I was really surprised The pain was on scale 1-10 only a 3. stayed in overnight, drain removed next morning and allowed home late afternoon. Seeing Mr Fox again in six weeks. The only symptoms I have at the moment is tingling down my arm into my fingers, I am hoping this is due to swelling in side. And I find it hard to sleep on my back. I am into my 4th day after op. and to be honest getting bored, I am moving my arm and shoulder ok, but not lifting or doing anything so that things can heal. But I am really pleased at long last one side's done, and when swelling goes down inside, hoping that pins and needles go. time will tell in the next few weeks. Keep you updated weekly on progress. It shows find a great surgeon and you are halfway there. do your research in your area. and don't be frightened to ask for the surgeon you want. it.s your body.
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I wanted to open a new discussion, to allow some space for those with Cervical Spondylosis (C/S) to simply express their opinions (including my own obviously) on how they think the C/S dynamics, and its progress over time actually results in the changeable symptoms they experience. I have my own ideas about how it all combines to produce the daily struggle we endure, but I'm also aware that opinions differ, and it might be a wise thing to do to consider other opinions, so that I get a more balanced overview. Same for everyone, I suppose.
I've had C/S a long time, over 30 years, and I've many of the different phases that are common to posters on this site, and other sites. One thing that strikes me is that most posters are in different phases of the condition, and although sympathy/empathy are nice things, they don't quite get into the area of finding or sharing suitable solutions for those differing experiences. What seems to be missing is a general overview, common to all, and acceptable to all, which would give a foundation to build suitable solutions upon. Some might even think that there are no solutions, except possibly medications or surgery....but, I personally, disagree with that, because I reckon that those possible but risky solutions are only relevant to certain grades of C/S.
The one thing that really stands out for me, after experiencing many different types of C/S phases, is that reasonable manageability always seems to return after difficult phases, and I'm inclined to ask questions about that because that is not a common feature of many other chronic conditions. It's like a rollercoaster effect, which in turn plays a bit of havoc with our expectations, and with our default settings for just getting by with the least possible disruption. It adds to the overall problem, by introducing a mindset that can't predict tomorrow's issues. Also, I think that just adds to an undermining of the decisions we might want to make in the present moment, decisions which might affect how tomorrow actually does evolve.
Just going back to the issue of 'phases' which pass, I've come round to seeing that as an attempted 'corrective' dynamic, whereby most of the symptoms we experience probably result from reactions to threats of nerve compression, and that those same symptoms have little to do with bone degeneration except in the sense that the threat to nerves wouldn't happen if there weren't any bone degeneration. I realise that some people with C/S have an underlying arthritic condition which increases degenerative rates, and thus increases symptom potential, but I still think it makes sense that symptoms result from threats to nerves rather than from spinal degeneration (although one causes the other, and the other causes the symptoms). By that definition, I think it's possible that even where there is serious degeneration, it doesn't necessarily mean the symptoms will get worse....unless there is accompanying increase of threat to nerves. Make sense ?
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Just got home a little while ago after a 10-hour day at the hospital. For anyone new to my situation, I was supposed to have an ovary removed that appeared to contain some type of mass, in addition to having a couple of small uterine polyps removed. My doctor ordered lab work on hormone levels and cancer markers that was all normal. She said that the mass was contained within the ovary and appeared to be solid. So this is everything we knew going into surgery.
Well, I had the surgery today, and guess what... there was nothing in the ovary! I was awake in the recovery room, and extremely dizzy, when my doctor came in with a big smile to tell me. She explained that I have a benign "floating" fibroid outside of my uterus that has been positioned in such a way that it has been pressing on the ovary. The ovary itself was a yellowish color, not the whitish color that it should be, but she said it was not the color that it would be if cancer was present. However, to be sure, she removed it and a frozen section was done on it that confirmed no cancer.
She also removed the two uterine polyps, in addition to a cervical polyp that also turned up, and these are all expected to be benign. The other ovary has a functional cyst present that she said will be gone in a few weeks. She also did a D&C as expected. The pathology results will be back on Monday or Tuesday.
I am still in total shock about the ovary. Since I was so dizzy when she told me, I couldn't process what the doctor told me at all. After they put me back in my day surgery room with my mom (I was allowed one person with me there), she explained it all to me. They gave me a pain pill and I slept for about 2 hours and then a nurse with really cold hands came in to wake me up. I had some juice and crackers, and a couple of cups of water, and after a while they made sure that I could urinate and sent me home. I'm staying with my family while I recover and they are a huge help.
So that is everything for now! I learned a lot today. It has been crazy and the outpatient day surgery unit was very noisy, so I am grateful to be home. I will have a follow-up appointment with the doctor on May 4, assuming that no emergencies or complications arise.
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can anyone help me understand the medical terminology used in my spine MRI report?
there is mild reversal of the cervical lordosis. at c 3-4 there is small right paracentral disc bulge mildly indenting the thecal sac. the cervical cord appears normal in caliber with no evidence of compression. normal caliber thoracic cord. conus medullaris terminates at the mid L1 level. there are single small T2 hyperintense foci within T1 and T12 vertebral bodies, which are inconspicuous on T1 weighted imaging, isointense to vertebral marrow, consistent with small hemangioma.
at SI joints, there is minor subchondral sclerosis evident on the sacral side, with low grade subchondral bone marrow edema evident anteriorly.
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My name is Gary. I am 57 and have had problems with hemorrhoids for years. It was getting to where I was spending two weeks out of the month basically ok due to constipation from opiate medication I have to take. Then one week where I use the prep H to push the roids back into place. Then often a week of just pain, stool softeners vs pain killers, and out of service.
I got referred to a surgeon recently and he said I had a bad case and set me up for surgery. They decided to do a colonistmy (colon probe. where I guess they pump you full of air and put a tube all the way up). I did not know that it was that extensive or I might of gone without it..at least not with this surgery.
I was told afterwards that I had some of the largest they had seen. Also the colon test showed some polyps they had to burn out. They did not look cancerous.
I had trouble getting cleaned out prior to surgery due to the pain and the opiates. As required I took 250 grams of miralax stool softener, 4 laxatives, and waited. I took them at 4 pm, had surgery lined up for 8:00 am with a 6:00am arrival. The drugs did not take effect until 1:00am so I was up until we had to leave for the hospital still on the toilet..and in severe pain.
I was still eliminating when we arrived. I was given a couple of ememas to use on myself. I couldn't hold them but they came out clear so they started the surgery, colon probe, and prostate exam.
I awoke after 2 hours of surgery. I was still under the anesthesia (I was put out) and not in terrible pain. I got up and was able to urinate. I had packing in me and was told to go home, take a bath, and they would come out. I had terrible cramps and gut pain, prostate pain, and severe anus pain. I have lots of stitches down there.
I went home and ate a small bowl of cereal and some oatmeal...and waited. I drank a bunch of juice and water but could not urinate. I was leaking blood everywhere. I took several baths and finally the packing came out. I took stool softeners and drank a lot. Finally the first meal, or what was left over from before, came out in the bath. I didn't have a full bowel push because of the pain but a bunch of crap, in small strings, some packing, and a huge amount of blood came out. I would say a pint.
I ate some more: a bacon and cheese bagel, some oatmeal, and stool softeners. I drank a bunch. I also had to take a bunch of painkillers. One the third day I had an involuntary bowel push but came up empty. I couldn't take the pain. Blood was still coming out in drips all the time with a small amount of feces. I called the doctor and got more pain killers. I set up a plan last night to have a bowel movement this morning. I ate some more oatmeal after one day without food. I took several sleeping pills and some painkillers to stop the urge to have a bowel movement. I had to get up at 12:00am and take more pain killers to stop an early bowel urge which would come up with nothing as is my experience. I awoke at 7:00am, as planned, and held the pain killers aside. I forced a bowel movement and produced a large pile of soft serve sh*t which was full of blood. There was more to come but, now 6 days out, I was in too much pain to push again.
It becomes a real fight to live. I am addicted to painkillers from years of degenerative disk disease and arthritis due to an 80 foot fall in 89. I don't get my refill until the 13th which is 3 more days. I have enough for today. I have stayed away from the long acting painkillers unless I run out. I hope to pass more later today. I will probably try the same procedure.
Again, it is the sixth day, and I still cannot walk without using the furniture. I try and move around as much as possible. I have some blood a fecal leakage which I clean up each time with a bath or a soaking wet warm wash cloth. Then I fold a washcloth in half and put in between my swollen cheeks until dry. They shave you down there and the stubble that grows back is very painful to the opposite side. I have never felt such pain. Each day has been a little better except for the third in which I was worse.
I would've still done the surgery if this all turns out ok. I will eat better, drink more, and do whatever I have to do to keep this from recurring.
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I am finally on my way to getting a long awaited L4-L5 Fusion. My doc decided on ALIF due to my previous L4/L5 Laminectomy (2003) creating a lot of scar tissue. That surgery was done posterior and it would not be a good thing to reopen the same L/4 area. I am relieved that this fusion is finally being done. My disc is about 98% gone and I deal with bone on bone pain daily in addition to bone spurs and osteoarthritis. However, I tolerate it pretty well. In addition to the L4/L5 issue, I also have 2 herniations in my neck and another few in my mid back. But these are secondary to my initial problem and need to take care of this fusion first and foremost. I read a lot of negatives about fusions on this board, but I try my best to think positively. Everyone is different and not every situation is similar. My plan is to help anyone I can with my experience and give support. I will try to post my progress after surgery. If anyone had recently (2013) had a ALIF fusion on L4/L5, I would like to hear about your experience. This will be a journey that I will not forget and I am planning on making it the best I can given the circumstances.
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I just got diagnosed this year with a Cholesteatoma, after a heavy mid ear inflammation in June, following a severe cold. Before that I had no problems with my ear.
My hearing was virtually lost during the inflammation but recovered pretty well, I guess only a 30 % has gone in my right ear. I live in Spain, in the mountains, and have no problems while I am here.
But I just visited the Peruvian Jungle, and it happened two times that after 3-4 days in the Jungle, my ear starts draining liquids and my eardrum perforates. After being treated two times with antibiotics in Peru, and moving to an area where the air is much dryer, the inflammation goes away within a week.
Now, last Friday I talked with my ENT specialist, and he has put me on a waiting list to have it surgically removed. According to him, it is a 'removal' operation, with a high chance of losing my right side hearing completely, as he 'thinks' the ossicles are infected.
When I asked him if a KTP laser is being used, the answer I got was that they don't use KTP laser in these kind of interventions in Spain.
Since I do not want to lose my hearing capacity in the right ear completely, I understood from reading about Cholesteatomas and treatments that a KTP laser assisted intervention has a high chance of preserving the ossicles, and thus hearing capacity.
There is an ENT specialist who has published about this, Dr. Fairley.
Does anybody has experience with him ?
Has anybody had this type of surgery with a KTP Laser ? How were the results ? I am very interesting in your story, As I am considering paying for the intervention myself in another country.
Prices are fluctuating a lot for this procedure, so if anyone knows a good ENT specialist (Cholesteatoma & KTP Laser) I would appreciate your opinion and experiences.
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I have just had 3 hemorrhoids worked on by THD surgery. This was done Thursday (and Saturday). I am on 2 sachets a day of movicol to soften stools but have not passed anything yet. I am eating fruit and little bit of other stuff such as digestive biscuits a little bit of bread etc. is there anything else I can do to help? When is pushing straining? I tried to go earlier and worryingly passed a jelly like lump of something?
The pain is manageable with occasional paracetamol or ibuprofen.
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On November 22, 2013, I had hammertoe surgery in my right foot. Incisions were made in the back of all four toes besides the big toe to release the tendon. The second toe was more rigid than all the others so it needed more work. Part of the knuckle had to be removed to slightly shorten the toe and a bone graph was put in. So, that toe had an incision in the back like the others and stitches on the top.
I was in a surgical shoe for four weeks, then tennis shoes for two weeks, then I could transition into other shoes. Recovery was pretty painful. I kept my foot elevated and iced it for the first week. I only walked when I had to use the restroom, and for the first few days that was almost impossible. It hurt so bad I ended up hopping to the bathroom on my other foot. So I got that surgery done in November and now it is March and my foot is doing great. Sometimes there is still slight pain in the second toe, it's still healing. My toes aren't 100% back to normal yet but I think they are close. I can walk/run on them with no problem.
I just had the same exact surgery on my left foot on February 28, 2014. This time I requested crutches since it was unbearable to walk on my foot the first time. I went home with crutches and used them for the first 4 days. Then on the 5th day I started to try to put pressure on my foot and begin to walk on it without the crutches. I thought the pain was getting better but it is now day 8 and I am in a lot of pain. My foot feels very hot, there is a burning sensation, and there are some stabbing pains. Usually the pain meds (Vicodin) help a lot with the pain. But tonight after taking one and seeing no improvement I took another, and still my foot is hurting very badly and I don't know what to do. Today is Friday and on Monday I have to go back to school so I'm trying to walk more and more everyday to prepare myself for having to walk around campus. I've already gone through this surgery before so I knew what to expect but so far the recovery for this foot has been slightly different from the first.
The pain is keeping me awake so I'm hoping it will ease off soon.
I would love to hear anyone's post-hammertoe surgery stories. Similarities or differences between our surgeries.
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I'm posting this (rather long) history of how I finally solved my hemorrhoids problem in the hopes it will help people who are still trying to figure it out.
I'm a 58 year old man in good health and at the correct weight for my height. I'm not on any prescription drugs, I eat sensibly and work out at least 2-3 times a week.
I've had hemorrhoids for many years and pretty much ignored them, but then about 3 years ago they started getting worse, eventually to the point where I had to do something because they started to affect my life style.
The lifestyle effects were mostly about physical exercise. For example, when I played more than 9 holes of golf, the hemorrhoids would start acting up and get so uncomfortable I couldn't focus on my game. Or playing racquetball for more than a half hour would cause the same problems. The symptoms were pain, sometimes some type of clear fluid discharge (I know - totally gross), and sometimes bleeding. I could actually feel the hemorrhoids stick out of my butt. The pain could last for several days and would be constantly on my mind to point where enough was enough, I had to get help.
So I got a referral from my regular doc to a colorectal doc. It was a bad experience... he examined me and afterward said, "Yup, you got a nice bunch of marbles down there," and told me I needed surgery and how painful it could be. His nurse told me that she'd had post-op patients call her and literally scream and swear at her because they were in so much pain. I left that office and never went back. I forgot about "getting better" and figured I'd just have to live with it for now.
But a month or two later I was playing softball at a meeting away from home and the hemorrhoids got real bad and when I got to the hotel they were bleeding and I had to go out to dinner with a bunch of associates, then get on a plane early the next morning. I didn't know if I'd be able to do either, but I somehow got through it and vowed to go back to the doc.
So I got a referral to another doc and he was a little better. But he too recommended surgery and told me there would be a 2 week period I'd have to take off from work. I still wasn't ready for that, but he did give me a very good key piece of advice, and that was to take one big tablespoon of orange flavored sugar-free Metamucil (he was very specific) mixed with a big glass of water once a day, and to drink lots of water each day. I started taking it the next day and it made a big difference in my bowel movements. They became much 'easier' and didn't bother my hemorrhoids nearly as much as before. That was about 18 months ago and I've taken it every day since (I think it's good for cholesterol reduction too as a side benefit).
Still searching for a non-surgical solution, I got a referral to another doc and the third time was the charm for the time being. This doc examined me and said I definitely didn't need surgery, that my main problem was a couple of internal hemorrhoids and they could be handled with rubber band litigation. I said what about the external ones that I could see with a mirror? He said those weren't the offenders, which was quite different from what the other two docs said. So he did the procedure. He picked the biggest one and put the band on it. It took about 5 minutes and was very uncomfortable but not painful. He told me that's it, that there's no after-care, there should be no pain and to come back in a couple of weeks.
Well, he was wrong about the pain. I woke up that night at 2 am in pain. I took a couple of Advil which didn't help much, so an hour later I took two Tylenols and that did the trick. The procedure had been on a Friday, so I couldn't call the doc to see why I was having pain, but I looked it up online and saw that it wasn't uncommon, especially if the rubber band had been placed too low, i.e., too far towards the lining of the rectum where it would pull on the wall.
I had to keep that up the meds for the next 2-3 days. The whole area was swollen and felt like a typical 'bad' attack, and I was bummed out thinking this wasn't going to work. On Monday, I called the office and found out they're closed on Mondays. Great.
On Tuesday things were starting to get better. There was still some pain but no big deal. I called the doc's nurse and she said I could come in, but it sounded like I was progressing ok and that yes, sometimes there is pain if the band is too low, and that's exactly what this sounded like. So I decided not to go in, and day by day it got better.
After about a week, I was back to working out, and for the first time in a long, long time, I didn't have hemorrhoid problems. I was now able to resume most activities without having those nagging problems anymore. What a relief!
I say 'most' because I still would have some minor problems after longer periods physical exertion, say after 3-4 hours, like a round of golf. But again, the issues were much less.
At 6 months after that first procedure I was still having some issues, so I decided to get another band done to get the second-worse internal hemorrhoid taken care of. I had it done, and this time there was no pain at all afterwards. The procedure was still uncomfortable, but now knowing what the result would be, I went into it with much less trepidation, and knew that even if I did have the same pain as the first time, it would be worth it.
So for me, it was all about getting those internal hemorrhoids dealt with. I still have the external ones, but much to my surprise they really don't cause any issues. I had always thought they were the culprits since I could see them, but I guess that's one of the pitfalls with self-diagnosis; the obvious answer was the wrong one. I may still have one more internal one to take care of, as the doc said they usual form in groups of three. But with the first two, worst ones taken care of, I think most of my problems are gone.
For any of you fellow sufferers out there, I hope you can learn something from these first experiences. The whole thing was embarrassing (to me) at first.... having those first docs checking me out 'down there' took some getting used to, but now I look at it as just another medical procedure, somewhat typical to what women have to go though their whole lives, or so my wife says.
About a year later and I was still having problems with at least one internal hemorrhoids. I went back to my doc who it put a rubber band on but it didn't help all that much. I went back again and he said well, there is another one, and I'll try to band it. I didn't really get what he was talking about with the try (he was never hesitant before) but said go ahead anyway. He said the issue was that he couldn't get the band all the way around the base of it but hopefully this would work. The next morning well sitting on the toilet, the band popped off. I realized that the banding procedure was no longer an option and thought that maybe it time to get surgery and get this finished once and for all.
I asked a separate doc that I trusted for a referral to a younger (<45) doc who knew all the latest procedures, as I was looking for the most non-invasive possible. I found one. When meeting with him he told me all the different techniques he uses and said that during surgery he'd decide which was best depending on how things presented themselves, and I was good with that approach.
I had the surgery and it turned out to be more complex than we thought. Initially, we knew there was at least one internal hemorrhoid that was the main culprit, but during surgery he found two other internals and one external. In fact, the main internal one was connected to the external one, so they both had to come out. So the surgery, which was in a full-blown operating room and I was completely unconscious, was rather extensive. Although it was scheduled to be outpatient I couldn't pee afterwards so they inserted a catheter and keep me overnight (The catheter insertion was weird and uncomfortable and freaked me out a little as a friend had just had one a month before and told me how awful it was. In reality, the fear from that was much worse than the actual procedure. But next time I would still ask for a Xanax or something first). I came home the next day in some pain. He gave me Percocet which helped quite a bit. (He started out with one 5 mg every six hours and it wasn't nearly enough. I had up it to two 10 mg every four hours for the first day or two.)
Here's the recovery process, which I wrote as it happened:
Day 1, Thursday Surgery @ 7:30 am. Prep was nothing to eat or drink after midnight and an enema the night before (more on that later). Woke up after, no pain yet but felt pressure in lower abdomen. Because of the catheter, they kept me overnight and removed it the following morning.
Day 2, Friday I went home, slept a lot, caught up Netflix (the one silver lining). Took 10 mg Percocet every 4-5 hours, which did a good job of containing pain. Was able to walk if needed, e.g., to the bathroom, but only felt like laying in bed. Total meds: 30 mg Percocet, 1 Senokot, 2 Colace, 2 Advil.
Day 3, Saturday - I'm now in the third day after the surgery and things seem to be getting better. I still haven't had a bowel movement which I am anticipating will be somewhat painful, But I'm looking forward to get through it because that will be kind of the last step. Total meds: 10 mg Percocet, 3 Colace, 3 Senokot, 1 Miralax, 2 Advil. (Might have taken more pain meds, but I was asleep quite a bit.)
Day 4, Sunday Had first bowel movement. Was more uncomfortable than painful and I wish I had been taking more stool softeners, because the surgical area is apparently swollen and theres not much room for stuff to exit. I upped my dose immediately to Colace 3x a day and one dose of Miralax before bed. The pain occurred afterward about 5 minutes after I was done, an aching started in the surgery area and got quite bad, to the point where I had to lay down in bed and wait for 10 mg of Percocet to kick in. Thank God for Percocet. From there on, I pre-medicated for the next few days which helped a lot. Had two more BMs that say, the 2nd followed by 2 Advil, 3rd by 2 Percocet. Total meds: 30 mg Percocets, 6 Advil, 5 Senokot, 3 Colace, 1 Miralax,
Day 5, Monday Stayed home from work. Sent email to direct reports why I was out (hadn't told them previously). Woke up at 6 am took 2 Advil. Took various softeners and pain killers throughout the day, had two BMs. Still painful with achiness but not as bad due to taking more softeners and stating ahead on the pain meds. Total meds: 6 Advil, 10 mg Percocet , 2 Colace, 2 Senokot, 1 Miralax.
Day 6, Tuesday - Getting a little better each day. Still stayed home for work, but had a one hour meeting downtown, so I went to that. It was good to be out. I had been noticing that there was a light hygiene issue with some minor staining and a little leakage, so my wife gave me a mini-pad that sticks to your underwear. It worked ok, but was hard to position properly. After that, I switched to the maxi-pads, which also stick to the underwear, but cover much more area and worked better. Good peace-of-mind as I didn't have to worry about being out in public. Had one BM, as I did from here on out. Total meds: 6 Advil, 2 Colace, 1 Percocet.
Day 7, Wednesday Back to work for the full day. Still a little awkward to get up and sit down, so I stayed at my desk most of the day, felt pretty good, maybe 80-85% better. If I had a job where I had to be on my feet all day, I would have stayed home again. Cut Colace down to 1, which was a mistake due to difficult BM the next day, immediately went back up to 3/day. Total meds: 4 Advil, 1 Colace.
After that first week, things continued to get better each day. I continued to have some achiness after each BM and took couple of Advil proceeding each one which helped. I went back to the doc for a checkup at the end of the 2nd week and he was pleased with progress. He said probably best not to take Advil as it causes bleeding, ok to take 2.5 or 5 mg of the Percocet, so I did that for a couple of days, then switched to Tylenol. I eventually stopped taking even that at about the 3-week mark. I continued to use the maxi-pads until about the 2-1/2 week mark. BMs at the end of the 3rd week were still a little difficult, especially to get them started. It felt like the opening wasn't big enough and I had to strain to get it going, but once stared it opened up and progressed normally. Maybe I was just too tensed up?
At the 4-week mark, the BMs are more normal with almost no straining. I was still taking 3 Colace a day, but considering going down to two. I should also mention that I was taking Metamucil 2x a day during the entire time period. I had been taking it once a day (1 heaping TB of the orange sugarless mixed in water) for the past several years on the recommendation of one of my first docs, and it helped a lot.
I also went back to playing racquetball just shy of the one-month anniversary. My doc cleared me after 2 weeks, but I was still too achy and just not ready. On my first day back to work, there was some pain from the BM (minor) and I was concerned that t would get worse when I played. I took a couple of Tylenol before playing and the pain was non existent. I was tired from not exercising for a month, but it was a good tired and, most importantly, no pain afterwards for the first time in years.
I should also mention that the hemorrhoid pain was gone after 3-4 weeks. It was hard to tell for the first 2-3 weeks, as there was pain form the surgery, but as it started to fade, I noticed that the old pain was no longer present after exercise of BMs. Yes! After all, this was the whole point in the first place, but it's sometimes difficult to remember as you're going through the post-op period.
Things I learned or wish I had known.
Surgery prep I was advised to do an enema 6 hours before surgery which I did (Actually the night before because the surgery was early). But looking back, I wish I had done a more extensive prep similar to a pre-colonoscopy exam, as that would have cleaned out everything and postponed the first BM for a day or two more. Maybe this isn't a viable option for some reason, but Id definitely ask the doc about it if I had to do it over.
Catheter - I was told there'd be a 50% chance of needing one because I'm a man over 50 (58). I wish I had just asked to have it inserted during the surgery, as it was stressful to have it done yet another procedure just 6 hours afterwards. And Id ask for a Xanax or Valium or something.
The recovery time is 6 weeks. Yes, it's possible to be back at work within a few days, but for me, it was really a couple of weeks before I was feeling anywhere near normal enough that I wasn't aware of the surgery, pressure, pain, the pad, etc. After 4 weeks, Id say I was 85-90% recovered. From all outside appearances I was 100%, and most of the time I was unaware of the event. To me, I'll be 100% recovered when I'm thinking/aware of the surgery 0% of the time. Put another way, Id say I was 100% functional 3-1/2 weeks afterwards, but 85% recovered. The 15% difference was that BMs were still an issue I was taking softeners still and there was some pain or achiness, but not much. I stopped taking pain meds for this at about the 3-1/2 to 4 week mark. I should also mention that, due to the softeners, the BMs happened almost first thing in the morning, typically after one cup of coffee. You should have access to a toilet because when I had to go I HAD to go. If I had had to wait more than a minute or two, it would have been a problem.
Because the recovery time is long, I was glad I had no big events or travel planned for a few weeks afterwards. We hosted Thanksgiving at my house exactly 3 weeks afterwards, which I had thought was a no brainer recovery-time-wise. It turned out fine, but I was glad it was at my house as I still wasn't 100%.
Id err on the side of more pain meds and definitely more stool softeners. I was warned that too many softeners could cause diarrhea, but I never experienced that, but I can definitely say that too few cause pain. For the pain meds, Id take them 1 hour before each BM for the first few weeks. Don't wait until afterwards because its too late. Be preemptive. Don't take Advil; take your prescribed meds or Tylenol.
Plan to be in bed for the first 4 days (day one being surgery). Although I was up and around by day three, it was really day 5 when I felt good enough to put away the tray table and resume downstairs life (our bedroom is upstairs).
Recovery clothing The only thing I was comfortable wearing for the first week was sweat pants. Unfortunately I only had two pair and they tend to get soiled easily in the first few days. I recommend having 5-6 pair available. And bring a soft, fluffy pillow to the surgery for the ride home. You'll be very glad to have it.
Was the surgery and pain worth it? Definitely. I knew what was coming more or less, but I really wish I had more details about recovery so I could set expectations, which I why I'm writing this in the hopes that it will help others. While the docs and nurses tell you about recovery, they don't really have the details, the day-to-day stuff. So here they are. Obviously, this surgery could be more or less invasive or extensive. Mine was a little more extensive than planned, but still, I feel like mine was a middle-of-the road case, maybe a 6 or 7 out of ten. A total guess really, but I had 3 internal and one external removed, so maybe you can judge by that.
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It is 10 days now since I had Open Myomectomy surgery. 32 Fibroids were removed, which surprised me, and I was in hospital for 5 nights. I am now home and getting stronger each day. The days before the surgery were anxious days but at the same time I was looking forward to the sugery and being free from the many symptons that fibroids cause. I had a great surgeon and anathestist and went fully prepared mentally, physically and spiritually for the surgery.
Surgery took 2 hours and remember being brought back to my hospital bed hooked up to IV fluids, catheter, oxygen and equipment on my legs to stop blood clots. Pain was minimal, similar to mild period pain and I was encouraged to use the Morphine pump to manage the pain for 2 days. Morphine did make me feel nauseated which is common. Once I was free from catheter and IVs on day 3 I was encouraged to do my Pelvic exercises and to walk around the hospital corridor. I was given paracetamol and ibuprophen at regular intervals and BP, tempearture and Pulse was moniored on a regular basis, which were all fine. I was encouraged to drink more fluids and had no issues with empyting my bladder or bowels so knew everything was working OK. Getting in and out of bed and sitting up was difficult during the first 5 days but became easier each day. Its amazing how much we rely on our stomach muscles for so many things. Once I was home on Day 6 I started doing very light duties around the house and a 10 minute walk outside plus regular naps whenever I felt fatigue. I can now do 15 minute walks and looking forward to getting stronger each day. I have some swelling around the incision but that is normal at this stage. Will see the surgeon 20 days after my surgery for post-op checks.
Overall my surgery went very well and I am very pleased with the progress I am making. Although Open Myomectomy is major surgery, becasue of the advance in technology, the skills of the surgeon and the excellent pain management and hospital care it is a much easier experience than I thouht it would be.
If you have been told by your consultant that you need Open Myomectomy surgery do not be afraid, focus on the positive aspects of being free of fibroids symptons, read up on the procedure, watch videos of the procedure if your that way inclined, understand the risks, prepare yourself physically and mentally and follow the advice given by your consultant on the aftercare.
I am grateful to God that my surgery went well and I am looking forward to getting back to the gym in dure course and having a better quality of life without fibroids.
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I had a prolapsed cervix and bladder a year after my hysterectomy. It is now going on two years post surgery. I am still having stitches break thru at the top of my vagina where my cervix was removed. It hurts! I'm going to the Doctor Monday, but very scared. I have moved and this will be the first time seeing him. Do any of you know what I will have to look forward too? What might he do?
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I'm 42 and i have just found out that i have this condition. The 1st doctor i saw after having an x ray didn't bother to tell me that i had this condition, and it was the next doctor that did. I have been having symptoms for the last year or so , which are dizziness, some numbness in my little finger and ring finger, neck ache, which is muscular and nerve extending to my shoulder and arm i have also been getting jaw ache, and i've had tension headaches for years.
i'm not sure if all these symptoms are due to having 2 ribs. i'm waiting to have an mri in october.
However i am seeing a 'sacral-cranial' osteopath who is really helping, and i am also having homeopathy which is also helping.
I'm not sure what is going to happen and it's comforting to know that there are others out there that will know what I'm talking about and who i can talk to.
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I have recently been told after 15 years of going to the doctors asking for help i have 2 cervical ribs and need to see a respiratory specialist.
I have been suffering with breathing problems which they did put down to asthma which might not be now, pains in my back, stomach, neck and arm. and sometimes get numbness in my arm and fingers.
I am cold and feel weak and tired all the time. I can sleep for days and still feel tired, the more i do the more i feel ill.
I have a large bone showing above my left collarbone which i can feel a large tube or vein above it going over the top of the bone which i measure to be about 2" wide.
Just wanted to know what the average size and width of cervical ribs.
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Have been suffering for 3 months with pain from cervical issues (diagnosed through MRI) - bulging discs, some stenosis, degenerative disk disease that is causing severe pain from neck through shoulder blade, underarm and down left arm. As I've had arthritis in my neck for a long time I know this pain came about from a stress injury to my neck. Have tried much conservative treatment (some physical therapy, chiropractic, and medication - currently 900 mg gabapentin and hydrocodone and ibuprofen and various others that I stopped.) I just had a Epidural Injection last week and thru this week experienced a bit of relief but not what I was hoping for. My question is has anyone gotten better with this type of problem doing these measures and had their problem resolve or at least get about 75% better without having any surgical intervention. My doctor thinks we can resolve this without surgery but also said surgery would be extensive as I have about 4/5 bad levels. I'm thinking of trying acupuncture and would appreciate anyone's input. Very tired of the pain and getting a bit depressed.
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I've been having pain and neck stiffness for years, and also have rheumatoid arthritis. Several months ago I started having "pins and needles" feeling in my left arm that became more and more intense from my shoulder down into my hand, mostly my thumb. I had an MRI, this is the result:
C2-3: There is a small posterior right lateral disc osteophyte complex as well as advanced facet arthropathy, particularly involving the right facet joint. This causes marked narrowing of the right neural foramen.
C3-4: There is moderate facet arthropathy, causing moderate narrowing of the left neural foramen. No evidence of canal stenosis. Right neural foramen appears patent.
C4-5: There is mild disc space narrowing and a right paracentral posterior disc/osteophyte complex causing minimal ventral impression on the thecal sac and mild narrowing of the right neural foramen. There is also moderate right facet arthropathy.
C5-6: There is advanced disc space narrowing, with prominent spurring both anteriorly and posteriorly. There is endplate sclerosis on both sides of the disc space. A prominent central posterior disc/osteophyte complex causes moderate to severe canal stenosis at this level with mild flattening of the cord. There is also moderate bilateral facet arthropathy. Neural foramina are significantly compromised at this level.
C6-7: There is a small posterior disc/osteophyte complex with minimal ventral impression on the thecal sac, but no significant canal stenosis or neural foraminal narrowing.
C7-T1: Normal.
OTHER: There is degeneration and narrowing at the C1-2 articulation with some irregularity of the dens.
CONCLUSION: Advanced degenerative disc disease involving the cervical spine, which is most severe at C5-6 with canal stenosis and bilateral neural foraminal narrowing at this level.
My doctor never called me, just sent me an email that said "no bulging disks, just arthritis", and he suggested I go see a pain management doctor. What should I do? I am having a really bad day today, my arm has been asleep more than it has been awake, and it's becoming more painful.
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I'm 48 suffered with cervical spondylosis for around 6 years, in the last two years it's got so painful. I have tried all meds, last year I had an op foraminotomy where they drilled the left side spurs C4 to C7. But the last year has been a nightmare the pain is worse. I have now had more MRI & CT scans more meds and having two injections next week. I asked the long term affect of my neck I was told I have a neck of a 70 year old. What dose this actually mean? Wheelchair what?? I am also on the list for a anterior cervical discectomy & fusion.
I have a fall time desk job which doesn't help at all but have a mortgage... holiday is taken as sick days.
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I am recovering from Anterior Cervical Discectomy, which became necessary to avoid drastic further deterioration.
I would like to tell you about my experience and what helped me. My problem started quite unexpectedly with a persistent back ache at work (I am an office worker). Within days it was so bad that I was vomiting with pain and had to stop working (I was commuting to London). I was on morphine within three weeks, but it did not help either. I won't list here all the various painkillers I was prescribed, which helped to certain extent, but the pain was so bad that I was suicidal. The doctors communicated with me hardly at all except writing another painkiller prescription. I felt totally abandoned by them. I tried osteopathy, ordinary physiotherapy and Bowen's therapy. Bowens worked the best but nothing would give more than a few hours relief from the extreme pain. My husband then hit on the Tens machine and that was the only thing that really helped. I would recommend it without hesitation. I dropped the morphine, which was a bit of nightmare for me anyway, and managed to live with the Tens machine.
Unfortunately my problem rapidly progressed to me losing strength from my arm and from my fingers and a neurologist recommended the dissection and fusion. It is not an easy fix, but to me it saved my life. I went back to work four months after the operation, seven months after first feeling the pain. I could not say I'm as good as new, but the pain has gone. My neck is stiff, gets tired very easily and a bit uncomfortable. I cannot lift, push or pull anything heavy. But I'm here, enjoying my family and grandchildren. I couldn't ask for more. I'm 63 and now feeling my age, that's all.
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I was diagnosed with cervical spondylitis when I was 27 ( had a severe fall when I was 16 yrs old...fell 2 stories), am 48 now and moved to Wales almost 2 yrs ago from South Africa and since being here, my pain has increased in intensity. Used to get steroid injections and am aware that I won't get that here in the U.K. I now suffer extreme nausea due to the pain and can only dry retch, as the valve below the oesophagus was tightened yrs ago and now prevents me from throwing up. I would appreciate if others with this condition could tell me what the maximum dosage of Ibuprofen one can take. Taking the normal dosage (2) does not alleviate the searing pain or spasms.
I am also very confused. After x-rays, all dr,s have said cervical spondylitis and not cervical spondylosis. Been told that I don't have arthritis and yet this is not ankylosing spondylitis, which 1 dr said it was..(he never saw the x-rays)...really confused even after numerous x-rays and dr,s. I am almost on the verge of giving up hope of getting effective painkillers from dr,s here. Do the exercises, use heated neck bags and nothing much helps, especially when I get a flare up.
Need to know if increased dosage of Ibuprofen would help.
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I have Bilateral Cervical Ribs. I also suffer Cervical headaches. Do the Cervical Headaches always come along with the ribs? Also, is it the Arthritis in the Cervical Ribs that are causing me so much agony? I have pain every single day. It gets so old, and boring. What does it take for them to remove them? I have a Kidney Disease as well, so I'm not able to take many pain meds, and the ones I have taken really don't do much of anything for me. I don't believe I have the TOS....think it would still be possible they would end up removing them WITHOUT having the TOS?
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I dont know i have cervical spondylosis , but MRI said i have a cervical spasm < now even after eating food my heart rate increase some times and there are weird feeling all day long in the chest ,pain in arm .. i feel tingling numbness, in legs ,arms , shouledrs some time. disbalance when i just stand up
Mty Doctors are sending me to neurologist,Cardio , Rheumatologist,Internal medicine .
nothing solved . Heart is ok , ECG is ok, x-ray of heart is ok.Blood test was ok ...
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