Double Inguinal Hernia Open Procedure Experience
Jan 11, 2015
Male, mid 50's,double inguinal hernia, open procedure.
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Day 1 no real pain until the meds/anesthesia wore off. Not too groggy.
Day 2-4 no pain when lying down, just when getting up. Then sharp pains in groin near upper thigh, really nasty pain. Right side, retained feeling everywhere. Left size all numb below scar, to and slightly onto thigh, and to base of penis. Balls not sore nor swollen. Advice, get a bed pee thingy if you drink a lot of water, it's a lifesaver.
Then onward, once the pain began to wear off a bit after about five days, I stopped pain meds and switched to advil. Nothing made much difference. I didn't have a bm until about five days after the surgery and was terrified. I was taking Colace and it worked fine. I drank a ton of water.
When I started getting up and walking, the sharp, burning, scraping pain was there when getting out and into bed. When walking it was like someone had put a brick in the left side of my groin. It was heavy and uncomfortable, probably due to the neuropathy. My nerve was not cut, I found out later, but it was all probably due to the fluid, swelling, and trauma of the nerve during surgery.
The progress here on in was extremely slow. A month in, still some paint, but less, still equal amount of numbness and discomfort when walking and sitting. After week three i could finally like on my side, which was great. This relieved the pain in my heels that were killing me from resting against the bed. And it ended the sore kidneys/back from lying around. A friend said socks can prevent this.
Week 5, still numb, but the heaviness in the groin feeling is getting slightly better. I went through a sort of depressive time after reading online about people who didn't recover well after a year or more. I'm feeling better these days, emotionally. After sitting/walking around for a couple hours, especially if I go out and walk, visit a store or anything like that, I get completely wiped out sort of all of a sudden. It feels like my entire energy is gone. Other people I ask say this is normal with surgery and it takes a long time to get the energy back. Saw doc and he said it seems everything is healing per normal. That was good, at least.
So I wanted to post this, because it seems some people are up and running marathons the day after whereas for some of us, the healing seems to take a lot longer than expected. Here's wishing everyone good recovery and mental strength. It is taxing to lie around and wonder if and when things will begin to improve.
My recommendations: Tons of water. Daily vitamins. Colace for first few days, then bran etc. Get a cheap bedside hospital table from walmart or somewhere, it's great for sliding over your stomach and putting a book or computer on. I also put it over my abdomen at night to keep the cat from jumping up onto me.
Bottom line, don't get depressed. Only after nearly five weeks did I begin to notice a real sort of improvement at all.
Last February I had a double inguinal hernia repair done and am currently on the waiting list to have my right inguinal hernia done again.
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this time I was told it would have to be open surgery and not key hole.
I have the pre operation appointment at the beginning of November and received a letter saying I'm on the waiting list.
But today I have received a letter with an appointment for a Anaesthetic Opinion? ? Dose anyone know what this is and why I have to have one. I'm 14 stone and 5ft 11 so I wouldn't have thought its cos of my weight as I feel I'm of normal average size/build.
Is anyone out there aware of any person who has had to have mesh removed due to mesh inguinodynia after inguinal hernia repair with mesh?
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18 months ago I had a spigelian hernia repair. Everything seemed to go well until the following April when I was in a lot of pain around the site of the op. I subsequently found that I had 2 more hernias, a femoral hernia and an inguinal hernia. Both were repaired at the same time last August. It transpired that the mesh had come away from my 1st repair and wrapped itself round my inguinal hernia but this wasn't discovered until the actual repair was carried out.
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Now I have similar pain and another hernia. My GP says that it is an incisional hernia and it is at the end of the scar from the last repair! I'm scared that the pain will become as bad as it was last year and worried for my job as I always seem to be off recovering from surgery.
How am I getting so many hernias? My consultant implies that it is because I smoke but surely that can't be the only cause!
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.
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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.
For approx. 10 years I've been dealing with internal and external haemorrhoids (rhoids) and the occasional prolapse - too embarrassed to seek medical attention I've just tried my hardest, despite the discomfort, to carry on regardless. After a recent defining moment in the bathroom I decided enough was enough and booked a visit to see my GP, which to my surprise was not as embarrassing as I thought it would be. Following a digital examination the GP confirmed that the usual solutions would not suffice and a referral to a Consultant was needed - fortunately I have private medical insurance and my appointment came through quickly.
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At my first appointment the Consultant completed a digital examination for himself and deduced that my rhoids were “quite large”. At this stage he suggested a Sigmoidoscopy (lower bowel camera) and ligation (banding) to see if that would help - whilst I was told the procedure is uncomfortable and not painful I opted for sedation on the basis that why would anyone choose to be in any discomfort when they really don’t need to be!?![/color]
Having researched the procedure online I returned to the hospital some 3 weeks later. I have to say the enema was a surprise in more ways than one – I now understand it’s a necessary requirement, but given the reason it’s being administered is it unreasonable to assume they would be a little more gentle? #Wowzers! Anyway, I waited around all morning and I was eventually taken to the Operating Room (OR). At this point I have to say Sedation is wonderful - I remember nothing between the fluid being injected in the cannula and subsequently being in the recovery room. Given I had been tinkered with all I can remember at this point is feeling as though I needed to go to the toilet. I was subsequently transferred back to my room where I remained for a couple of hours in a little discomfort, but I recall being in pain – the Consultant came to say he would see me at my follow-up appointment and I was eventually released by a nurse that said “it looks like you’re coming back to see us” and I spotted THD on her paperwork.
It was about 2-3 weeks when I had a follow-up with my Consultant, which gave me lots of time to read up on what THD was etc. – compared to the rhoidectomy of yesteryear it sounded like an absolute gem of a procedure. The Consultant asked how I had got on with the ligation and I explained there had been no real change however, he said he didn’t think it would work given the size of the rhoids – so we discussed returning for a THD in 2 weeks’ time. So, there is the background…
I returned to the hospital for my THD last Friday and, given the procedural information I had read on line, I was feeling quite good about it. Having had another fairly uncomfortable enema (by the hands of the person that delivered the previous one! #Ouch) I was told that I was 2nd on the list and would be seen quite quickly – it was roughly mid-morning when I walked to the OR. At this point I was given the cannula etc. before the GA was administered. Quick question: Is it just me that likes that dizzy lightheaded feeling you get with a GA? I’ve had a few in my time and I really enjoy it!
]The next thing I remember is waking up in the Recovery Room with an overwhelming feeling that I needed a bowel movement (BM) – I’m talking that real desperate need somebody has when they have a stomach upset. I recall one nurse saying it’s probably the packing and the other said the consultant did not use any – I was then told somebody was on their way to transfer me to my room but I could have a bed pan if I needed it. I was quickly returned to my room and I asked if I was able to go to the toilet – I was told I could, but needless to say I actually couldn’t do either of the things one usually does when they visit the lavatory!
After a good hour or so I asked if any pain relief was available as I was really quite uncomfortable. I was subsequently given codeine, which did help – mainly because I fell asleep if I’m honest! I was woken by a nurse wanting to take my obs – I said I needed the loo first and the nurse agreed to return within several minutes. I managed to urinate however, upon returning to the room the nurse had quite a fright as found me lying on the bed looking as white as the pillow case, feeling dizzy and sweating – I was given Oxygen for a while. I was given more codeine later on and, after more sleep, I eventually saw the Consultant who said that he would see me again in a couple of weeks, but with regard to that day I could stay overnight or go home. Being tired as I was unable to get any decent sleep, I opted to go home at around 18:30. Upon check out I was prescribed Fybogel (to be taken Twice Daily) and Paracetamol (as and when) – due to other ailments I have access to Co Codamol 30/500 and Tramadol hence I was good to go. The journey home was not too bad however, the left side of my rectum was particularly sore hence I sat with all my weight on the right bottom cheek for the duration. When at home I pretty much spent the evening sleeping, thinking about the toilet or trying to go to the toilet!
I woke up several times in the night with the feeling that I needed to go to the toilet, so I eventually got up to watch TV at around 04:30. Feeling the need to go to toilet lasted all day – other than briefly after passing wind or a short while longer after taking a Tramadol. I eventually went for a very small BM however, it was quite painful to be honest and I wondered if my body was telling me I needed to but my head was telling me not to – I was literally having spasms, such a weird feeling that happened several times throughout the day. The good news was that whilst I still felt rough, I was more mobile and thought THD may just be the best thing since sliced bread.
Pretty much mirrors Day two having woken up at 04:00. I went downstairs and eventually managed to go to the toilet for a small BM however, it was soooo painful I felt exhausted afterward. I returned to bed mid-morning for a couple of hours and then remained in the confines of my house for the rest of the day.
Woke up at a reasonable time and managed to potter around the house all day. Took a 40 minute drive to take my child to school and back and noticed that the desperate urge to go to the toilet has been replaced with a fullness/weight feeling and there is now an aching on the left side of my rectum. I managed to do the smallest of BM’s, which, in the main, was probably my body dispelling some of the Fybogel! In cleaning myself I noticed a small lump on my rectum, which I can only liken to an external rhoid – brilliant, just brilliant! By the afternoon I actually felt like I was in pain until I read about and decided to take a sitz bath – temporarily relieving the pain, until I took more Tramadol
Today. I’m feeling somewhat down about my post THD experience. It doesn’t seem to be consistent with the majority of literature that says you’ll be running marathons within 48 hours (slight exaggeration, but you know what I mean)! I’ve got what I think is an external rhoid, the left side of my rectum is uncomfortable, and when I sit down or stand up I can feel pressure - like you do when the rhoids are playing up…not to mention that after I drove my child to school today I felt like I’d received a swift kick up the arse when I got back to the house. I had a BM this afternoon and it was painful…AGAIN…I ended up elevating my feet on a footstool to making the passing of the BM more comfortable!
Having got all that of my chest, I’m hoping somebody can offer an opinion on the following…[/color]
Could the lump on my rectum be linked to the procedure and shrink over time? I’m wondering if I’ve not noticed before as I previously had a prolapse?
Could the lump be a new rhoid or hematoma given the constant feeling of requiring the loo and then my associated attempts to go?
Given I’m now at Day 5, should I really have an aching feeling where I think the procedure was completed?
Given I’m still uncomfortable, would you contact the GP or carry on taking the tramadol for now?
I’m off work at the moment, but I will need a sick note in 2 days – is it likely that I’ll be ready to go back at this point?
Many thanks for reading and, where you can, replying with your comment(s).
I was diagnosed some years ago with Hiatus Hernia and have had 3 endoscopy's. I do eat carefully am about 1-2 stone over wieght, I am a line dancer and have no problem with that. The main thing that I don't like is the feeling of a lump under my right rib, it is quite uncomfortable and i feel i have to stretch up to ease it. I can feel it now while sitting at the computer. I had the pain in backand chest last night which is bad but took Peptac liquid which quietened it down. Does anyone else have the lump feeling?
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I have an inguinal lymph node that is enlarged. 2cm long verified by ultrasound. It has been like this for 7 weeks now. Pain started in June with testicle pain. Doctor diagnosed epididymitis. All testing came back negative. Eventually testicle pain went away but turned into groin pain in mid July. This prompted ultrasound that found enlarged lymph node in groin. The doctors deemed the lymph node as questionable. My doctor said it is nothing to worry about. My concern is that it is causing minor discomfort since mid July in the node itself as well as my upper right thigh, my right hip, and also in the area on my right side between hip and ribs. My doctor says the node is not an issue and I may have an inguinal hernia that is pressing on my femoral nerve causing referred pain. I think my lymph node hurts and whatever is causing it seems to be spreading. My doctor is not worried at all. I'm freaked out. I have no night sweats but I'm so scared that I barely eat or sleep. I lost 10 pounds my doctor said from stress. I gained it all back afterwards. Does this sound like lymphoma? My doctor thinks I'm paranoid and tells me not to worry. I am freaked out because it feels like no one cares or believes I'm in pain.
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I would like to know if it is normal to have abdominal pain after an orchiectomy. I have had an inguinal orchiectomy 4 days ago and I have testicular cancer. When I cough the pain is very bad it feels like muscle strain. I had back pain for a few days on the same side too but that has now passed. I'm worried that something is seriously wrong. Has anyone else experienced this pain after surgery?
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My doctor pretty much acted horrifically shocked at my weight gain (double in weight in less than a year) but will not help me get off mirtazapine. I'm sat here in tears. I can't win ! I have episodes so vile and destructive and they're getting worse because I'm disgusted by my vile appearance.. I can't win ? What can I do ? The one person who should be able to help me is ignoring my pleas ..
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I'm heartbroken. Either I sleep and keep getting fat which equals being exhausted every time I leave my house and never fitting into my clothes and being so ashamed of myself my depression starts up again OR I return to sleepless nights (meaning paranoia and unusual sleeping patterns grumpiness) but be slim again and comfortable going out in my own skin..
I'm so lost.. I never knew how badly this drug could affect someone.. My entire life has vanished because I hate myself and I get so sweaty and out of breath everytime I walk up the stairs.. I have tried to just NOT eat but it makes me so miserable the hunger.. I can't cope. I'm so bloody disgusted by myself
Ive got no way out, i've gotten into this awful hole and i've got no way to get out im stuck i hate what i've become i don't know what to do,
I'm 42. Weight is 133. Mother of 4. Recovering from double mastectomy. My problem is now that I do not have any breasts my ribs really bulge out just below where a bra would sit. It really looks like the top of a beer gut. My movement is still limited. Please advise on exercise and number of reps to give a flatter belly and more curvy sides. Also to strengthen the collar bone area. I've looked online but I'm not sure of the reps because I do not want to bulk up- just tone
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Had this op performed by Mr Reece at Queen Elizabeth Hospital in Glasgow just over 3 weeks ago. I have 8 screws and two cages in my disc space packed with synthetic bone grafts and injected with bone marrow taken from my vertebrae.
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I was up walking the same day, baby steps buy nonetheless, walking. I was in hospital for 4 days (I would have been out earlier if my bowels had moved sooner).
The first 2 weeks were pretty uncomfortable. Very sore to move as the front stomach wound was very swollen and tight. Once this initial period passed things became easier.
I can now get up from lying in bed or on the couch without much pain, it's still there in the background but not all controlling.
I'm walking everyday, not far but doing this a number of times.
I'm taking this recovery very slowly as this is last go at resolving my back pain after having two previous surgeries on the same site (S1-L4).
Only sitting for very brief spells, not driving yet due to wound, plus sitting does bring on the pain. I have had some nerve pain down my left leg, probably every few days or so but it settles after some meds.
I am still on my nerve pain meds as the damage from previous surgeries won't be fixed by the op. Also still on Dihydrocodeine 60mg X 4 daily but I'll try and reduce these over the coming months.
Would I say that it's been successful? Yes! I have greatly reduced back pain which was my dominant pain source.
It is a major decision to have this op but I had been through all conservative methods previously which didn't assist at all.
Hopefully things will continue to improve over the coming weeks and months. I'll report back over this timescale.
After a 4 year wait, I finally had a consultation with an orthopedic surgeon. He said I was a good candidate for cheilectomy. But after reading all the horror stories on these boards, I wonder if I should even have this surgery!
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Most days, my pain is tolerable. I walk quite a bit, try to run at least twice a week and cycle every day. The running part is the worst : the most I can do now is 15 minutes. But I love running! Even had the fantasy of running a marathon before I turn 50. That's why I am considering surgery. I hope to regain a little range of motion and lower pain.
Has anyone had good results? Is it possible to run after a cheilectomy? How long does it take to be able to run again after surgery? Does the bone spurs grow back? How is the long term prognosis?
I'm 48 years old and can't keep up with my mom who is 74 ... I have to do something! Can anyone help me decide if cheilectomy is right for me?
How did you pick a breast pump?
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I'm thinking double breast pump but what brand, what store, what price?
I'll return to work at 6 weeks and want a pump that'll make it easy at work to pump. we have a mother's room and I'll get time to pump but want a good one.
I've had a squint all my life (30 years) had two previous surgeries that did not work. My right eye turns inward.
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Recently I was referred to hospital for Botox treatment. This was carried out 9 days ago.
My eye is now straight. (Yay) I am however suffering from double vision when I look to the left and what I can only describe as slight 'ghost' double images (not constant) that seems to appear randomly and when looking in any direction,
Has anyone had Botox and experienced something similar? I'm just looking for reassurance that the double vision will pass and I can continue with the Botox treatment?
The botox kicked in 3 days after it was administered so I've only had double vision for about 6 days.
I've had this for about five years now and it affects the vision in my right eye - straight lines are wavy, etc. The worst thing is the double vision I get, as the image I get from each eye is different. I've still to find anybody who has, or has had, this and would really like to compare notes with somebody about it.
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Back in October 2014, I experienced angina and went to the ER. Assessment indicated that I had blockages in some cardiac arteries, and a double bypass was performed. I was started on a med regimen of Metoprolol 25 mg/day, Lipitor 40 mg/day, and Aspirin 81 mg/day. As I recovered from the surgery, I discovered that I now had erectile dysfunction, a numb feeling in my penis, and reduced libido. When I told my cardiologist about this, he switched my BP med to Bystolic 2.5 mg/day. Supposedly, Bystolic doesn't have sexual side-effects. Though I can now get a partial erection and can have an orgasm, it takes a fair amount of stimulation and the orgasm is not as satisfying as it was prior to starting on medication. I'm 62, have no other health conditions or medications, was never on BP or cholesterol meds prior to my operation, and never before had any problems with erectile dysfunction. On both Metoprolol and Bystolic my BP reduced to an average level of about 115/75. My cardiologist proposed a trial of Viagra, but I declined as I do not believe in treating a side effect with another med that has potential for additional side-effects. Nonetheless, this condition is unacceptable to me, and I would want to get off a medication with this side effect. Has anyone else experienced similar side effects on Bystolic? Might the ED be the result of the Lipitor reducing cholesterol which, in turn, disrupted normal testosterone synthesis?
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I had a double bunionectomy on December 10th. I'm healing fine, but my problem now is from wearing the post-surgical boots. I was told I would need them for walking for 6 weeks. I'm trying to spend as little time as possible on my feet, but when I walk I can feel all the pressure on the outside and heel of my foot. It doesn't bother me during the day, but every night around 2 or 3 a.m. I'm awakened with searing pain on the outside of both my feet. It's excruciating! Has anybody else had this problem, and if so do you have any suggestions on how to prevent/ease the pain? I'm trying to get back to work, but it's frustrating when I'm not getting enough sleep.
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Was diagnosed with pmr a year ago by my family doctor, was put on 15mg prednisone and my entire life changed, the pain was gone and my quality of life restored. Was sent to a rheumatologist to confirm diagnosis and was Told there was nothing wrong with me and to discontinue prednisone. My gp agreed to keep me on it. Here's the problem, my gp now wants me to taper down to 5mg. About the same time as the pmr diagnosis I also started having problems with my eyes, blurred and double vision, this condition has gotten quite bad and I'm really struggling with my vision. I have been checked out by eye specialist and mri and told nothing is wrong. I'm at the end of my rope and just don't know what to do. The tapering of the prednisone is not going well as the pain is all coming back again, and I just can't
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keep going through this. I feel like the doctors don't believe me and have nowhere to turn. I know that I can not go back to living a life of existence only. Is there anyone out there that can help me?
I just went to the doctor who was very happy with my flexion and bending. He told me I don't even need PT any longer and to keep walking, swimming and doing whatever it is I've been doing. The last time I was measured I was about 120-122 in both knees. I had double knee replacement. My gait is good. I do not limp. This last week I have walked, stood and climbed steps more and at night have really paid the price. I had two nights where I really was unable to sleep because of the aching and pains going down the shins from the knees. I've iced and used heat but unhappy about this. The next day was difficult to walk. I'm feeling like one step forward two steps back. My husband says this is just "part of the healing process" and to just keep going. It's depressing, though. I'm tired of being in pain and want to move on with my life and be able to walk 1-2 miles without being incapacitated the next day. I was also told that I would just need Tylenol or Aleve at this point for pain but.....doesn't put a dent in the night pain. Anyone else experienced this?
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I really don't know how it happened or if it was caused during sex. But my clit slit opened. and i don't know what i should do. It did not hurt at all or did i bleed. Is this normal? and im trying to think since when it became like that...
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