Endometriosis :: Abdomen / Leg Pain After Total Hysterectomy
Apr 23, 2012
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 had a hysterectomy done in February of 2013, I had a partial, just my uterus and cervix removed so all that is left are my ovaries. Within the past month all of the same symptoms are back that I had before surgery. Severe pelvic pain, bloating, back pain, not sleeping, hurts to urinate and so on. I'm 27 years old and no kids and I felt it was my only option because I had so many laps done and there was nothing more to do other than the hysterectomy. So if there are some women out there that has had a full hysterectomy could you please tell me if its worth asking doctor to remove ovaries. Could really use some advice now or just to know there's more women out there around my age going through the same thing. Thanks for taking the time to read.
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I had a total robotic hysterectomy on 11/17/14. after my 6wk ok for sex, it was very painful, bleeding,watery dishcharge, felt something inside my vag. I went to dr. an he said I had scar tissue and possibly didn't get all my cervix(how is that poss)so he put silver nitrate on it and I went back 4wks. said I still had some so put more silver nitrate on.. went back 2 wks later, said it was all gone and didn't see cervix & I didn't feel anything either (was ok for sex)we had sex 1x and very easy. was painful but not horrible. haven't since until 4/28/15. it was horrible, bleeding, cramps, excruciating pain. deep thrusts especially. since ive had watery yellow discharge (some odor)again -so much its like I pee myself-not pee, and feel a hard, thin something inside vag. (tongue shaped)when i touch it or move it, I instantly cramp bad. I need to know what is going on, y I cant have sex (never had prob presurgery)could it be torn cuff? is that my cervix still left?
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I just saw a Urogynecologist yesterday who says I need a total vaginal hysterectomy. Of course, I am scared! They did Urodynamics study and my bladder is OK. I originally thought when I went in that my bladder was falling. That's what my GYN at home told me. Not true according to this St. Louis doc. His name is Dr. Veronikis at Mercy hospital. Would love to hear from anyone who has info on him. I haven't scheduled the surgery yet. Still thinking, praying, researching, etc. until I decide. My prob is that my uterus is falling down and pushing out my vagina. Quite an ugly sight!! lol He will do a TVH and repair the vagina. Let me hear from anyone who has stories to tell or similar experiences.
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I was given a sick note for 6 weeks but my husband is wanting me to return after 4 weeks.
Said I won't need 6 weeks as i am different now to when I had op 10 days ago so won't need 6 weeks.
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I had a total robotic hysterectomy 5 weeks ago. Sunday night had unplanned sex. It was not painful, I'd say uncomfortable. When my husband ejaculated, it burned!
Today, Wed. Still burning, uncomfortable and frequent urination.
Does this sound like an infection? Or irritation because it was too soon.
I even resorted to using hydrocortisone last night because it was driving me crazy and I could not sleep.
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Last night 23 September I kept getting pulling pains in my abdomen, my last period was from the 7th till the 11th of September so it's not period pains, what could it be?
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I had a vasectomy 11 days ago. I rested, stayed off my feet mostly for a few days, used ice packs, all the ordered behaviors. My incision still hasn't healed well despite wearing compression shorts for 9 days. On about day 8 I started applying antibacterial cream and breathable sterile pad taped down over the incision to prevent infection (and was also on antibiotics for a sinus infection). There was no sign of infection, no visible sign of hematoma. But the incision remains a bit raw, like a split lip that seeps. The dissolvable stitches mostly came out within 6-9 days.
However, my right teste or epididymis is extremely sore still (I felt better from day 4-8 except when sitting a lot), swollen and riding high. When I sit upright for awhile at work, I also get an acute pain in my right inguinal area about 6" in from the hip bone. It feels like a nerve issue. It twinges and throbs when I stand and today is even making walking painful.
Any thoughts? Acute epididymitis? Sperm granuloma? Nerve damage? Normal recovery? I had a single-incision closed vas with excision, clips and cauterization.
I agree with the copious comments on the web -- the urologists need to do a FAR better job with the honest assessment of recovery. I was under the impression that this would all be largely resolved within 3-4 days. Instead, the past 3 days just keep getting worse with no clear self-diagnosis. I'm calling my urologist again tomorrow and insisting on a checkup....
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I've been having pain in my right lower abdomen for some time now and did some tests and all seem clear. Today I went to a surgeon who tested me and said all feels very normal. Since my dad had colon cancer at 56 he suggested I do a colonoscopy just to make sure there is nothing. I need to wait till the 20th April and I'm already freaking out. Will they tell me immediately after the colonoscopy if something is wrong? I'm 39 with 2 kids and always assume the worst that I have cancer.
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I went to the hospital a week ago and was diagnosed with a UTI. Since then I've continued to have sharp pain in the lower left area of my abdomen, under my ribcage (and just general side pain and some bloating)- and a dull pain in my back. Along with that, for the past couple of days I've felt nauseous off and on, weak, extremely tired, and today I felt like I was close to passing out when I was in a store. Could this still just be the UTI? Or possibly now moved on to a Kidney Infection, or... Thoughts?
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I'm not sure where to start. A lot has been going on in the past month. It all started when I started to feel like I had a couple of drinks when I had not. I was able to calm myself down because I thought I might be having some sort of anxiety attack. Long story short the symptoms did not go away. So I saw my doctor last week. With my vague answers to his questions he mentioned he wanted to do some further testing. Part of the testing was blood work and a 24 hour urine. That was last Wednesday. I had the blood draw on Thursday and turn my 24 hour urine and on Friday morning. It just so happened that I started my period on Friday. Its normal for me to feel a lot of lower back pain during my periods. this time is a little different. I started to feel the lower back pain then the pain moved to my upper abdomen on the left side. Then the pain moved to my lower right side of my back. now the pain is back on the left side of my upper abdomen. Of course everything that I have been reading leads to one thing... Pancreas. after calling my doctor my blood work has come back normal. However my urine test has not come back yet. They told me it could take up to a week. In the past this pain may have been here and it has gone away. But because of how much reading I have been doing on whyI have been feeling funny I've noticed the back pain and the abdomen pain a little more.
I have an appointment tomorrow afternoon. However I'm really scared.
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I have been diagnosed recently with this as an adult. I am a little confused as my pain is in my upper abdomen, right in the middle, about 2 inches above my belly button and below the ribs. Anyone else get pain here?
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I'm 33 5/7 I have been having bad lower back pain and abdominal and it goes through my thighs which makes them feel sore I didn't do anything out of the normal today but when I try to stand I can't stand straight. Anyone know what it could be?
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I'm a 18 year old guy with no previous illnesses of any kind, don't drink/smoke, etc. Except not exercising and sleep irregularly, I'm pretty okay with lifestyle.
I had the symptoms of a UTI one day (first time in my life) with symptoms of blood in urine and lower abdomen pain. My doctor diagnosed it as prostatitis and gave me antibiotics for a month.
I never had the symptoms again since the first day of antibiotics, but now that I'm 3 weeks in, I'm feeling new symptoms like hesitation to go urinate, want to go urinate more often, etc.... Maybe it's my mind playing with me, but I FEEL like my bladders feel a little weird. Like, it feels... full? There's no pain at all, except perhaps minor irritation in my testes.
So now I'm really wondering if I should go see the doctor again, mostly in fear of potential kidney damages (urea poisoning a possibility?) I don't have insurance, but won't hesitate to stomach the bill myself if need be. Since I don't want to end up in the ER, or die...
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4 days after a no-scalpel vasectomy, I have significant bilateral pain in my right testical, abdomen and back. Doc says it is just recovering from the surgery, said I should take 600mg Advil every six hours for 5 days. I'm worried this is the start of post-vasectomy pain syndrome. Anybody experience this?
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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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Last week I went to the hospital because my stools were black. They tested for blood but found none. Blood tests showed slightly elevated liver enzymes so they did an US and diagnosed me with fatty liver. That evening I began to notice swelling/faint pain in my upper right abdomen. I thought it was because of all the pressure from the US. It's been a week and it seems it's only gotten worse. Pain/swelling feeling extends from below the rib cage, don't my right side and i also get intermittent pain in my right lower back.
Once I got the diagnosis I changed my diet and stopped drinking. I'll be honest I used to eat horribly. Fast food, frozen meals, high fat, sodium and sugar. I became almost addicted to minute maid lemonade and drank 1-2 liters a day. All that HFCS is what I think mostly contributed to the fatty liver. I don't drink all that often (although when I did it was usually heavy). 2 years ago I used to drink a lot (though still only on the weekends) but up until my diagnosis it would be maybe few times a month tops.
I'm beginning to worry that they misdiagnosed fatty liver and it's something more sinister like cirrhosis. Other symptoms include fatigue, sometimes when I breathe I can take a full breath but it's like I'm not getting enough oxygen. It's hard to describe, almost as if the swelling in my abdomen is crowding my lungs. Lastly, my stools are now very light brown and loose (I honestly can't remember the last time I had a normal BM). I have a follow up with a GI Dr but that's not for 3 weeks. All of this has triggered some severe health anxiety that I once had as a child after an oral surgery.
Does anyone with fatty liver experience this feeling of swelling, abdominal bloating and pain in the upper right abdomen, right side and lower right back?
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In my last 2 cycles I have noticed more changes than usual for me. I have started spotting about a week before my period and have pain almost from ovulation onward each cycle. I have been tired most of the time, temps are all over the place even after ovulation, have a combo of diarrhea and constipation as well as an influx of acne. I do have a Drs appointment but I have to wait a month to see her. Anyone else had anything similar? I usually have painful periods but not usually all month long and many symptoms of Endo, just never been diagnosed with it as of yet.
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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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