Endometriosis Laparoscopy Too Much Pain On Sitting And Laying On Sides
Jul 30, 2015
I had a successful Diagnostic Laparoscopy for suspected Endometriosis under general anesthesia in a general hospital and it was done in a little over one hour, I remained in recovery care for 4 hours due to pain and low blood pressure procedure was done yesterday (29th) fortunately doctor was able to treat all the areas/spots that contained Endometriosis growth/adhesions, she made 4 incisions and said that the procedure was smooth and successful. I've been home for roughly 22 hours now. I had a catheter so I'm left with a moderate burning and discomfort which seems to slowly be wearing off in my urethra it's naturally very narrow but thankfully I am able to urinate regardless of the Burning and the discomfort which I was told to expect. I managed to drink mint tea, water, juice and a light meal yesterday though I didn't have much of an appetite and I haven't eaten today either I just don't feel like it at all did this happen to any of you ladies? I am consistent with the pain and anti-inflammatory meds that I have prescribed for me due to the amount of pain I am in. So far I'm in bed laying on my back either resting or sleeping I feel incredibly exhausted. I have a follow up in 4 weeks or so with my doctor and I have her cell number as well which is comforting. Now I just want to know am I the only one who couldn't sit the first day of the surgery? If I force myself to sit I.e when I go to the bathroom I'm in so much pain and it kinda got worse after I got home probably due to the wearing off of the anesthesia. All I know for sure is sitting and the mere attempt of laying on my sides results in lots of pain and the only comforting and least painful position is to lay back down on my back with my head slightly elevated and my feet as well. My abdominal area feels awfully sore and.....
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Long story short, I've been suffering from excruciatingly debilitating cramps every single cycle,this started three ish years ago I spend hours in the ER I've been admitted few times as well and it's the same bloody routine every single time
I'm in immobilizing pain, cold and hot flashes, nausea, vomiting fainting poor appetite dehydration low blood sugar levels heart palpitations weakness fatigue exhaustion crankiness moody insomnia etc etc
All these symptoms I experience up to two weeks before my period then during the first 3-4 days of my period then total exhaustion few days after my period and I'm symptom free a week before my period give and take. I should also mention that I've had several x-rays, ultrasounds and all kinds of blood tests and everything comes out good healthy and no problems yet I have these symptoms that just don't seem to go away, last stop for me was a visit to an endocrinologist and he's taking care of my thyroid problem given a new doze a little over a month ago and things are looking fine on that end I had a referral from him to see a gynecologist in mid September but having been bed bound with all the symptoms and persistent pain on my right abdomen I spent the night in the hospital and everything came out good both the blood and the urine tests and the ultrasound and regardless of how many drugs were given to me via an IV I was still experiencing bad persistent tedious excruciatingly painful pain on the right side of my abdomen so the gynecologist today discussed laparoscopy with me and I felt so comfortable around her and being as fed up as I am with all this pain I said I'll go for it
It will be a Diagnostic Laparoscopy for Endometriosis she put it as urgent and she'll be the one performing the procedure I'm happy things will finally start to clear out and hopefully I'll be in my way to some kind of cure hopefully but I'm so nervous please help any words of comfort or advice will be greatly appreciated. I did half the paper work already and I'll have some more to do the day of I have a really good doctor guiding me thru this call me weak or crazy but I'm incredibly nervous.
It would be nice to hear from anyone who's done this kind of procedure please BTW I'm 23 years old, healthy no health complications non smoker or drinker
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I am 11 weeks post op. Yesterday I started with pain on both sides of my Bikini line still got it today now the pain is really bad. Since UFE I have had these pains but only when I am on a period. This time there is no bleeding my last period was 2 weeks ago and the previous one was 2 weeks early. I had UFE done Jan 18. January and February periods where heavy but a month apart. This is the first time I have had the pain without the period wonder if anyone else has had this. Gonna get some pain relief of GP just wanted to know if this is normal.
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My symptoms were abdominal pain on left and right sides as well as diarrhea and constipation. Which turned to flat stools after that subsided.
After a CT, a colonoscopy with fasting AND prep, my results came back normal, yet my stool is still flat consistently. I'm worried and confused because people say this is cancer but others say IBS
Is this kind of occurrence of always flat stools possible with IBS?
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38 weeks pregnant lost a tiny bit of mucus plug and sometimes feel pressure in pelvis/vagina area pushing down when im sitting and when i walk for i get pain in both sides of my thighs feels like a nerve is pulling which makes me bend. Im also getting hard stomach with no pain and i get light lower back pain. What is this? Please help.
* will i be dilated now that im having pressure? I went for a check up a week ago and midwife said my cervix is closed. What does that mean too?
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I'm now 7 weeks off the 6 month mark. Today is not a good day had pains both sides of my bikini line even the meds won't shift them. Thought I was past this fed up.
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I'm 27, I got ejected out of a car at 17. I broke my hip and shattered my pelvis. My first surgery was to reconstruct my pelvis than a year later I had a total hip replacement. I hurt every single day, the worst pain is from sitting to standing and walking that initial step on my bad hip is excruciating. I don't take pain meds anymore if anyone has any tip for pain relief.
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Can anyone advise me? I had my first PS op last June '09. I am still experiencing pain when sitting for any length of time - whether in office for the day - or on car journey. I have not had recurrence of actual opening of the wound itself (altho it took a long time to close) and no abscess' - but the discomfort frightens me that it could be coming back! My GP tells me to wait and see for a while!
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My daughter has very big problem. She is 23 years old and she has Endometriosis. This is very painful for her, but her gynecologist told her that is early stadium and that this problem is not yet in faze for surgery. He told her to take Aspirin and Ibuprofen if she has big pains. She has terrible pains since yesterday and I am wondering should she, maybe, take Cataflam.
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I have been presumptively diagnosed with endometriosis for the past 8 months, meaning I haven't had a laparoscopy to confirm. My pain is usually a gnawing/aching pelvic pain concentrated around my inner right hip bone. It can make it cumbersome to eat and move, and will eventually build up to create anxiety and fatigue.
Suddenly, I've been having very strong pain on my right side (again near my hip bone, but also higher and more general). This pain is sharp, sudden, and paralyzing. It will leave me shaking, gasping, and frightened to move again (as if moving might make it worse).
I am concerned about taking the endometriosis NSAIDs I have, in case this pain is from something else. (?)
LADIES WITH ENDOMETRIOSIS, have you ever had pain that feels like this? What does your pain feel like?
[The pain I'm having makes me imagine a small blade is sitting just inside my hip bone, and, when I move, it cuts into the tissue around it (miserable right?)]
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I ended up in the ER last week after having lower left abdominal pain and severe lower back pain. I have had pain on and off for the past 4 months. The cycle of pain seems consistent - starting mid-cycle and relief the first day of my period (of course one pain is just substituted for another since I have bad cramping but I prefer the cramping to the mid-cycle pain).
This month as been by far the worst and now I'm having pain radiating up and down my left leg and thigh. The only thing that seems to help is sleep and pain meds only take the edge off.
After having an external/internal ultrasound, the ER doc thought it's most likely Endo- which is really frustrating since there doesn't seem to be an end in sight. I'm already on BC- the Nuvaring, so I don't think there will be any quick solutions with BC pills.
My questions: How common is sciatica with Endo? Are there better BC pills/shots/etc. that will help the Endo symptoms?
I've NEVER had any reproductive issues until last September when they found Adenocarcinoma in Situ on my cervix from a stubborn HPV infection. It's been one thing after another since my colposcopies and cone biopsy. I've read that Cone biopsies can actually make you significantly more prone to developing Endo since it can narrow and scar your cervix and not allow for period blood to escape the uterus.
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mri 5 weeks ago
L4/L5 broad based posterior disc protrusion contacting transiting nerve roots
L5/S1 disc dehydration mild disc bulge probable annular tear.
Just seen neurosurgeon who says back and leg pain not caused by this where is pain coming from then.
pain burning lower and middle back and buttocks weakness In legs.
Chronic pain on walking,sitting,lying down or twisting please help
Scheduled another mri as soon as possible
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I am 26. I work in some IT company, and i have sitting job. now I am suffering from sever lower back pain. Doctor said that it is due to long time sitting work. What to do?
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October of 2014 my primary doctor discovered that I had endo after 6 years of painful periods. I had a laparoscopy on may 13th to gain a better idea on how bad it was. they found fluid floating around from a cyst that was on my right ovary that had ruptured. my left ovary was huge, filled with fluid and its also completely attaches to my bowel. now my GYN said that they just cleaned up the fluids and did not want to remove my left ovary because i am so young (20yrs old). she put me on a BC, camrese to calm the endo and I started taking it on may 17th. for a few days now i have been having symptoms like when I am about to have my period. since yesterday I have been feeling nauseous and both of my ovaries started to hurt. By today the pain has gotten worse. it feels like my ovaries are about to explode. I notice that when I urinate or move my bowel, a little bit of pressure is relieved. the pain is getting unbearable and I don't even have an appetite. I still have 32 more active pills until its my break week. anyone have any idea what could it be? I am scared that its something serious.
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I had a total hysterectomy due to endometriosis. i was put on climaval hrt patches after which caused headaches and pains and i was then changed to livial approx a year ago but for the last 2 to 3 months i have started to experience the abdomen pains, back pains, leg aches, exhaustion, joint pains and bloating etc that i had before my hysterectomy. its not as bad but its still bad enough to cause problems to my everyday life and routine especially with my 4 year old daughter here. please could anyone recommend any other hrt or treatment for hysterectomy after endometrial? i am now taking my co codamol and voltaren tablets for the pain that i was on before my op!
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I've been having pain sitting, standing, & walking very far (at all) for over a year now. I had a spinal fusion done at the L -5/S -1 level back in 2002, & my docs keep close tabs on my back. I've had a tiny tear in the L-4 for many years, but most the docs feel my current problem has absolutely nothing to do with my spine - I agree. I have been diagnosed with a hip labral tear in my right hip socket about 4 months ago, but not bothered enough to do the drastic surgery. Doc injected left hip socket due to pain, but again, not my main problem.
I've had physical therapy (which aggravated the left socket), steroid injections into the ischial tuberosity bursa (both sides) - due to the doc thinking probable ischial tuberosity bursitis, which it is not, & am scheduled for an EMG down both sides of my lumbar spine (I hate those tests - they really hurt!). Meanwhile, I've been working with my chiropractor who does adjustments, percussion massage, iontophoresis, & cold laser treatment on me twice a week.
NO ONE knows what this is, WHERE to send me, or how to FIX it!
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Im 19 yr old I have an a back pain from last 3 month . I m computer engineer most of the time I spend my time on computer .give me a medicine name who made my pain relief
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I have been very ill and in a lot of pain since August, going backwards and forwards to my doctors, even got admitted to hospital in August with suspected appendicitis but got sent home.
However last weekend I got rushed into hospital with awful sharp pains in my right side of pelvis and ended up having a laparoscopy where they found a cyst that had ruptured and leaked fluid all around my ovary so they had to cut me lower down to clean it all out and remove the sack! I was in hospital for 2 nights being sick and in pain.
I came home last Tuesday night and have had horrific shoulder pain from the gas and I can't manage to walk more than a couple of mins without getting shooting pains where I've been cut and being exhausted after.
I've been signed off work for 2 weeks, I'm a nursery nurse so a lot of lifting, sitting on the floor and getting up and down is involved! I'm worried I won't be better by next week and will need more time off, how long was you off work for with this or similar procedure? Any tips to speed up my recovery?
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I've noticed for years that if I lay down when I feel an aura coming on, no matter how intense it gets, I won't black out & go into a full blown T/C. Usually after a T/C my brain seems to.....how should I say.....reset itself as far as "knowing" how intense the last aura was....with every C/P I have they get more & more intense every time I have one until I would black out from one and end up in a T/C. Strange thing though, I've noticed that everytime I'm sitting or standing after they get so intense, I'd fall and go into one. If I lay down on the floor, after awhile, no matter how intense the C/P (AKA aura as far as I'm concerned) gets, it suddenly goes away after a bit. Anyone else ever notice this? Why could this be? I've tried to ask a handful of Neuros. but they NEVER give me time. Everything is "You have any seizures lately? Let's get a blood level. OK see me in ___ months." And that's pretty much the extent of the visit! They NEVER want to let me ask anything else (I've seen 7 or 8 in my life, so I don't think things are any different anywhere. And I'm not the only one I know who gets this attitude.) Anyone have any idea WHY this "pattern" would happen? Could it be more oxygen getting to the brain? More blood?
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When I get up in the morning my ears are blocked (especially the right one),they clear within about an hour and stay clear during the day. I have been using olive oil for about a week now - as suggested by my doctor but it is not making any difference.
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Hi ladies lately i have been having a lot of breathing problems I am always shortness of breath even when just laying around. I am 16 weeks and not even really showing is this something normal or should I be worried
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