Ovary, Uterine / Cervical Polyps Removal - My Experience
Apr 7, 2016
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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The nasal polyps were very unpleasant, causing continual blocked nose together with the sensation of the polyp moving as I breathed. I had them removed by surgery and it was completely pain free throughout, although the anaesthetic injection was a bit sharp. I had no postoperative pain at all and only a trace of bleeding.
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I have recently become anaemic, I suffer from uterine polyps that have been 'quiet' for about 6 years ever since menopause, however about a week ago I started bleeding heavily, the past couple of days I am so tired, wobbly on my feet and look as white as a sheet, also heartrate is up a bit, anyone out there who has experienced the same or similar? and what happened regarding treatment were you put on iron tablets etc? I know I have to see the doc and will be ringing her tomorrow but am sitting in bed fretting about it.
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I have had breast cancer and have been on lupron shots. I can't be on these shots forever so my doctor and I Have talked about tubal and ovary removal. I have had terrible joint pain in my knees from the shots which prevent me from walking and doing the active sports I love to do. Has anyone who has had this surgery experienced the same joint pain and have long term problems?
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I (have) had Thoracic outlet syndrome. It took approx 8 years to figure out what I had. Finally found a doctor I could agree with. He found cervical ribs both right and left. Only had symptoms on my right side. Pretty sure symptoms were brought on by a car accident (whiplash). Anyway.. Had the cervical rib removed and the first rib removed along with the scalene muscle that was in a spasm. It has been 5 weeks and I am still taking pain meds, although I am finally starting to feel some relief. Not ready to quit the pain meds though. Although I'm gonna have to since my dr wants me off them. Wish he could feel this pain. My chest is numb but it is painful underneath. It burns like heck and the muscles, or it may be the fascia that runs from my neck to my chest that is so tight it kills me. I try to do my stretches but it hurts. Mornings are awful. Be prepared to not sleep at first. I am thankful to have found this site. You feel like you are the only one out there who has been through this since it is such a rare anomaly. If you are going to have this surgery prepare yourself for not only the pain but the mental challenge of being in pain for so long. You will have some really down days.
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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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Back in 2012 i had a fibroid embolisation performed it stop my periods after 3 months.But brought on the early menopause at the age of 46 which i was told would not happen. My fibroid shrunk and my belly went down to has it was the size of a cricket ball on my left side and sitting on my bladder.
3 years later i am back at my Gp with back ache and pain in my right hip and after a scan i have another fibroid sitting in the front wall of my uterus which is at the moment the size of a golf ball.
I have two options removal of my uterine tubes or to take Esmya for 3 months,i don't know which to do has i was under the impression that being on the menopause n the embolisation would prevent any more fibroids occurring. Im 50 next year do i take the Esmya and hope no more return or go for the opp?
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I would like to know about anyone who is six months post op. Just to know if it worked and if you lost any weight and got rid of heavy periods and anemia.
I would like to lose at least 22 1bs as I feel it's Fiboriod weight.
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So I had my myomectomy last weds evening. I was nervous as hell and cried in whilst the anesthetist was tending to me. They gave me an epidural to make me more comfortable and which meant I would need less 'hard' drugs after surgery lol as they didn't want me to take too much morphine Etc.
When I came round they told me my consultant had removed 13 fibroids. I had 14 so I was immediately in my drunken state questioning them as to what she had done with number 14 turns out she left maybe 1-1.5 behind as they were small and she didn't want to risk damaging my uterus.
The next day I felt surprisingly good and wasn't really in any discomfort. I found out this was cos of the epi. I was itching though which is a side effect.
I had some off days generally with trapped wind and a feeling that my tummy was very very tight and being pulled in all directions which wasn't pleasant but it's now day seven after surgery and I'm managing to control the pain with just paracetamol. I refused ibuprofen two days ago as they were giving me gastric pain.
I can't get comfortable that much in bed as my back hurts quite a bit which might be a side effect of the epidural not sure but all in all I'm not too bad. My consultant has been amazing. She was coming to see me most nights in hospital even around 10pm to check on me. She is pleased with all and how it looks and I'm finally back home since last night and am to go back to her in 5 weeks. They told me its a very slowly healing process and I had a BIG op but slowly slowly I'll get there
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4 days ago I had open abdominal myomectomy resulting in the removal of 22 fibroids i was previously on esmya to reduce the size if them which worked by reducing my womb from 20 weeks to 16 weeks in size.
It took 3hrs I had a epidural also as the anesthetist said it would help reduce blood loss
I'm home now with prescription of tramadol and paracetamol
I have staple like closures feel like Frankenstein bride.
The pain is pretty bad but I'm hopeful I'll be up and better soon.after being suffering for 8years of heavy bleeding iron transfusions pain depression embarrassing accidents.etc
I'll keep you all updated on my recovery..
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Just thought I would post an update I'm 4 weeks post op. For the 1st 3 weeks I was bleeding on and off now it seems to have stopped. So hopefully next period will be normal. My stomach is so much better as well I no longer feel bloated it's also getting flatter not much but definitely there. Still have low energy but hopeful that will go as time goes on. My leg aches a bit when I walk my dog but it's gradually getting easier. Overall though really happy and I would recommend this procedure to anyone. Much better than a Hysterectomy
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I'm now 11 weeks post op. I have got my energy back so something is going right. Periods are heavy but not flooding last one was 18th March so I'm hoping the next one is gonna be at least 2 weeks off. Had a twinge of pain this morning but it went. There is definitely shrinkage on my tummy area but it gets bloated back to size when I am due a period. It's a lot better though as before the op I could not eat properly if I did my stomach would really hurt for ages after and bloat so much that I felt like I would burst. I would definitely recommend this op to anyone as its better than having a total hysterectomy where they take out the womb cervix and ovaries.
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On the 18th August it will have been a year since my myomectomy..
In the last year I've gained all the weight I lost in my 5 months of being unable to eat solid food.
I have a couple of questions. Firstly I am still very sensitive above my scar, is that normal?
Secondly, I still get a lot of swelling above the scar even a year on. I know that's to be expected but it quite uncomfortable.
Thirdly obviously where I had lost the weight, that has left my scar very tight where I lost so much much and regained it.
Finally my periods are very heavy again and I frequently get bad back ache (even without PMT). Should I still be getting back ache? ( I was going to have physio but moved house so it's not within the boundary).
Lastly on a different but related note. In May I was 3 months pregnant obviously mentioned my op just in case. Announced to the family etc and that evening began having a miscarriage. After a long time in A&E, a loads of scans telling me I most likely had a fibroid again I was left in a canteen and given 2 paracetamol and lost my baby there. The pain was pretty horrendous and I spent 10 hours in hospital, A&E were good, being moved to gynecology was horrific. Will the NHS ever apologies or have any empathy at all for either scenarios? Just because I am not screaming does not mean I'm not in pain the positive is I have my life back, changed my career and began to get myself fitter. I have made some life changing decisions.
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I had an operation on 21 Nov 2015, this is to share my experience on those people who are nervous as I did before the surgery
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I was diagnosed with gallstones and I been eating the same way I was before the symptoms went away, until today, I am really worried on how my life and diet will change? And positive thoughts on your experience?
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1. You will feel tired, bloated and in pain after the operation. I felt very nauseous for a few days and unable to eat. This is normal and is the effect of the anaesthetic used during the operation combined with strong painkillers. It will pass after a few days, try to sip water frequently to flush out the toxins.
2. The nursing staff are very helpful and concerned with your wellbeing. If you don't feel ready to go home, say so, you know your body better than anyone. I stayed in for 7 days in the end as I was in a lot of pain and had severe swelling. Don't be afraid to ask!
3 The nursing staff will remove the dressings after 3 days and if like me you have ster-strips underneath these will come off on day 5 or 6. When I removed mine the wound bled a little, but it was nothing serious and the nurse put a temporary bandage on for 2 days until it stopped. You will be shocked at the size of the wound. Mine reached from my pubic bone to above my belly button. It does start to look better after a few weeks and once healed, I will be using lots of bio oil to help it fade.
4. You will have trouble having a bowel movement. Constipation is normal following a major operation, a combination of painkillers and lack of movement. Drink plenty of fluids combined with a healthy diet (lots of fruit & vegetables). Try to move around as much as possible. Go for short walks once you feel stronger at least once a day. If like me you still haven't been after several days you could try LAXIDO and or LACTULOSE, both effective at clearing any blockage. It worked for me
5. Take the painkillers they give you, they will help. Try to take them at the start of the pain, not when it has you in its grip (not so effective). Only stop them when you feel you can cope without them, don't try and be brave.
6. If you have had your ovaries removed you will suddenly go into the menopause. I am having terrible night sweats now, which keep waking me up I bought a summer quilt 4.5 tog and am using a fan, to keep cool, it helps. I am trying to cope without HRT due to a family history of female cancer and will be trying natural herbal supplements instead. Hope they help
7. Lets be honest it will hurt and I am only starting to feel better after 3 weeks. I expect to be off work for at least another month, as my job is quite physical, and my muscles/wound are far from healed, but every day I feel stronger and I am off the painkillers now. I go for a short walk every day and potter around the house. My wound is healing nicely (its not pretty) but at least my alien is gone!
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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'm 37 years old. I've been diagnosed with PCOS and Hashimoto's (autoimmune thyroid disease) when I was 25. My symptoms include: weight gain, water retention, leg swelling, hair loss, awful hirsutism, bloating, periodically growing cysts, and periodic urinary tract pain.
I don't eat red meat and dairy. I try to limit processed carbohydrates consumption (bread, pasta etc). I sometimes eat soy products but they don't go well with my thyroid. I don't exercise enough.
All the above mentioned symptoms have gotten worse in the last 13 months. I have a "beard" that I need to remove at least twice a week. I went from 125 lbs (56 kg) to 139 lbs (63 kg)! I can't fit into my clothes at all. My calves get so swelled during the day, I gave up wearing boots in winter and wearing skirts, because the look huge.
Right now, I'm having one of my "flairs". My right ovary is burning and so is the rest of my abdomen, urinary tract included.
Doctors are always happy with my results. And oddly enough my blood tests always come back normal. Hormones included, except the estrogen that seems to be on the (acceptably) lower side. I haven't tested my levels of DHT. (My doctors never prescribe that test. Well, they never prescribe the one for estrogen; I paid for that one myself a few weeks ago). Whenever I have an ultrasound they confirm the PCOS as well as the fact that my right ovary is enlarged. But they’re never worried.
My thyroid therapy seems to be off. My endo changed it two months ago, from levothyrox to euthyral (combination of T3 and T4). And I don't feel great. I always feel a lump in my throat. I'm experiencing lack of energy and enthusiasm (too little thyroid hormone), along with occasional heart palpitations (too much thyroid hormone). It was supposed to make me feel better and help the weight loss. It made me feel worse with the mixed symptoms of hypo and hyper thyroid.
I'm thinking about fasting (juice/water), going raw, eating only during 8H a day (mostly veggies nad fish), eliminating gluten all together.
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My endorsement thickness is 6.4 mm at 13th day and right ovary small and left ovary follicles. is this normal?
we are trying for baby. My age is 29 .
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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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