Future Of Atrophic Vaginitis For Five Years?
Apr 9, 2014
I suffered with this terrible condition and went through hell till I was prescribed Climagest 2mg and Vagifem which has now been changed to Ortho Gynest as Vagifem was discontinued. The medication changed my life. I am like a new woman. My consultant told me it was only safe to take for five years and now a month away from being taken off it. I am getting in a state of panic thinking of going back to suffering. What is my future ? Is there anything else I can be offered. I am also looking at natural alternatives. Read a lot about carlson's Vit E and DHEA caps. Any advice from anyone that could help ease my mind about the future of my condition would be helpful
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Have posted before this Xmas saying things haven't been too bad, and that's right. But things changed earlier today when I felt a fire building up in my Vagina! Anyway I used one of my Suppositories and sat quietly for half an hour and the burning was easing! It's about the quickest I have ever known a suppository to work! It's not perfect but before I used the suppository my discomfort, on a scale of 1 - 10 was 10. After using the suppository, it's down to about 1.
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I really don't know what to do, i just made another apt for second opinion on hrt. I have alot of symptoms and much anxiety and don't know what to do. Both success and unsuccessful tries of these hormones will be much appreciated.I
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I ordered four packs of the Key E suppositories from US because they were so much cheaper ( then got walloped with £18 in import duty so no they weren't) and ordered some Tea Tree suppositories at the same time as I had read how these were soothing.
Tried one yesterday and as expected very tingly but by last night I was dry as a bone, sore and today burning up like crazy so will not be using these again. Back to the Key E and coconut oil for me
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I saw my doctor last week and she said she had just been to a menopause seminar where the continual use of vagifem was discussed to treat VA. She said that there have not been any long term effects and that patients could use it twice a week for an indefinite time.
She also said that if a patient stopped taking it the recurrence of VA could be severe and much harder to treat going forward.
I asked about the Mona Lisa laser treatment but she had not heard of this.
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I think about this almost 24 seven. Some days I just sit around the house trying to avoid symptoms.I feel like i'm stuck as I still don't know how bad it will get,can I deal with this or should I give in and start the hrt..so many unknowns
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I have just started using vagifem and was pleased to find it did not irritate me (I have extremely sensitive skin down there and can only tolerate natural oils). However, after the second day of use I got thrush. I am susceptible to thrush and during the perimenopause, with hormones in chaos, I would get it every few months despite being on a no sugar diet and taking lots of anti-candida supplements. I had been getting slowly dryer down there. I have not had a period for 51 days and since my last period suddenly became completely dry down there. Sexual intercourse has to be short, careful and aided by loads of oil based lube, but it still hurts and I am sore after. Having suffered from vulvodynia caused by repeated and persistent thrush I am wary about thrush and damage in that area. Water based vaginal moisturisers sting me and oil based doesn't rehydrate the cells. So, after trying various things without success and my GP warning me it will get worse, I have bitten the bullet and tried vagifem. However, I am worried that it may have caused the thrush. Has anyone else experienced thrush caused by vagifem? Did it persist? Or did it settle down once your body had adjusted to the oestrogen, or once you had dropped down to twice a week doses (I am still on 1 a day).
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Anyone else feel depressed about this situation.My husband is the type that wants to be busy all the time.With this new problem..well realtively new..the atrophy,I have anxiety every day I wake up not knowing if I will feel good enough to go to the store,out to eat,trips etc.He on the other hand wants to be constantly on the go.I still have not decided to take HRT yet,so thus the confusion.I am really scared I will make the wrong choice as what to do about the therapy as well.I have had 3 different doctor opinions so far and that is depressing as it only confused me more,plus all the money its costing.Guess I could use some encourageing words.Thanks.I thought I sailed through menopause and it was over,didnt even know about atrophy..what a surprise and not a good one!
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Burning vagina constantly like sensitive burning bit itchy in vagina. No thrush no infection. One test bit blood under microscope. Pressure to pee and good flow each time. Doc referred to specialist. Very worried. Postmenopause.
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I went to my doctor today,again got a few answers but not many.This is about my sixth trip about vaginal atrophy.I would ask her questions,got a few..i have never heard that..vitamin e,costs of HRT treatment,I mentioned the Mona Lisa's Smile treatment.She has not heard of that either.She wrote it down and I believe she was quite anxious to look it up.I wonder why some doctors don't like us looking up things on the net,they should be doing the same.I would think they could learn many new things from the computer.
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I have been having lower abdominal discomfort, burning and mild itching for the past three years. It seems like I have got a urine infection but tests came clear. I also seem to have slight vaginal discharge. My GP referred me to a gynae and he could not find anything wrong, vaginal swab and urine test came normal. I asked about AV and he did a blood test for oestrogen and this cave normal and he said I have not got AV. Everything seems quite healthy down there except I keep suffering from this burning sensation and discomfort. I keep going to my GP and she said I have got AV and prescribed me Ovestin cream which I used last year & did not help, I was having hot flushes and sore breasts. Today I went to see her again as this burning sensation was driving me crazy. She prescribed the cream again, I do not know whether it will help or should I give it another go.
I was also surprised that I had blood in my urine and suffered two urine infections without me knowing. Although I suffer from burning sensation, it does not burn when I pass urine and I have got a good flow. She also treated me for thrush with no effect. In the end she took a swab and it came negative although the nurse said she could see thick white discharge up. I have come to the conclusion the slight discharge I suffer does not mean I have thrush. Looking at the symptoms of AV, it does seem I have got it. Now who do I believe the consultant or my GP. The consultant did quite a few tests like ultra sound and probing my vagina with something I cannt remember what it was last year. Strange when I was on holiday for three weeks, no symptoms, it only bothers me when I am idle and watching TV. I am also concerned I might suffer with urine infection without me knowing due to this burning sensation. Aftet two lots of antibiotics for urine infections and cream for thrush, I am still the same.
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Saw my Doc earlier and spoke about the Vit E Capsules and how good they are for VA. Said I know they obviously aren't poisonous but I told her I had been using some up inside even though there were some concerns about the gelatin shell. Straight away she was very eager for me to stop using the capsules because she said the shell wouldn't break down. Then of course there was the subject of not using something inside that's meant to be swallowed. But thing is, how does she know the gelatin shell won't break down?! Anyway she gave me a prescription for R.....s and I am using it now so I will see how I get on.
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I am not sure whether I suffer from AV GP thinks so but have never asked the gynae. Was discharged 2 yrs ago. Problems are constant burning abdominal discomfort feeling of having urine infection and since yesterday spotting brown discharge and I feel so uncomfortable down below something is not quite right. Just want to know whether spotting is one of the signs of AV. Been in and out of A&E due to a trip and hurt rt shoulder and not too keen to go and see GP again, it seems I am there almost everyday.
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i have read on here that Vit E suppositories can be very helpful in treating the dryness in the vagina. I have had numerous treatments off my doctor but suffer from side effects making it difficult to continue with treatment on a regular basis. I have given up on intercourse altogether and am only 57 and live with my partner who is very patient but I know misses the physical side of our relationship. I would love to find something that would make it possible for us to return to a more physical relationship again. Has anyone been successful in using this treatment?
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When i drink..sometimes urethra burns..irritation vulva etc..anyone else?
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when I had vulvodynia in 2013, I researched everything that could be contributing to it. One thing was the chemicals in toilet paper. In order to produce the pulp from the wood to make the paper harsh chemicals are used, typically caustic soda and sodium sulfide. This "chemical pulp" is then bleached, the colour or scent may be added. Could these residual chemicals in toilet paper be contributing to the irritation experienced with VA? Would you put caustic soda (drain cleaner) or bleach on your vulva, even if you didn't have VA?
Since I had vulvodynia I have used toilet paper that is made without nasty chemicals and without bleach to wipe after I've had a wee.
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I'm 25, a stay at home mum to 3. I've had problems with my back for a few years now which was put down to spinal stenosis. I've been in and out the gym for a long time, but I started to enjoy running in the morning too. My back then started to get worse, so I was referred for physiotherapy.
At the end of November to the start of December 2015 I started to get sciatica symptoms, it started just over a week after I started physio, I kept going for a few weeks which was difficult but I wanted to give myself a good start at recovering. I got very bad very quickly on the 18th Feb, I couldn't do anything without being in agony. I was admitted to hospital for a week to try manage the pain, I was given an injection into the nerve ending and sent home. This worked for a day!
The symptoms came back with a vengeance, I couldn't do anything, walking only to the toilet, which I'm ashamed to say I didn't make it in time every time. I couldn't sit up. I spend my time on my front with my knees tucked under me, it was the only position that reduced the pain to make it easier to deal with. I was on 50mg of mst, taking oramorph every couple of hours, and a few other meds. My gp was amazing though, he could see the pain was too much, and instead of a referral to surgery, he called a spinal surgeon himself. After getting an appointment the following week the surgeon agreed I needed urgent surgery, thankfully! After my pre assessments I has my discectomy. date for the 14th April 2016! So I've been lucky to be seen to soon.
The surgery went to plan, they done all they had to and without any problems. My blood pressure and heart rate caused some issues after the surgery, BP too low, heart rate too high. I was given 2 drips which did improve it temporarily. The results were instant, the pain had reduced, I could sit and walk the next day. There was pain, but nowhere near as substantial. I was sent home 2 days post op, on the ground i my pain medication from the gp Monday morning.
Today is Monday, since I've come home I've felt a whole lot worse, i feel ill. I struggle to eat, I keep getting dizzy spells, my heart keeps going crazy, hot flushes, then coldness. If it weren't for this, the recovery would be so much easier. I'm hoping it corrects itself, and doesn't warrant a visit to the gp. I feel I've overdone it and my leg has been very painful today, since this afternoon I've done nothing but worry about my future. Will I recover? Will it get bad again? Will I have a good quality of life? I only found out just before my op there are 3 damaged discs the middle one l4/l5 is the one that herniated. What would that mean for my future? Will that cause more problems?
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I'm 24 years old and my teeth and quite badly grinded down, my whole life I have been grinding my teeth have just never been able to stop, it was much worse when I was younger and in my teenage years but I still can't help but do it. To make things worse I have been looking for a partner recently due to being alone pretty much my whole life and I feel like I will never find somebody having teeth like this, they are straight and don't have big gaps or anything but a fair bit is missing. I did all this damage to myself as a kid when I was too stupid to know better and try harder and now I may be alone forever I feel so ugly, I'm not exactly attractive anyway. The insecurity and worrying about my future is getting too much.
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I am 24yrs mum with my 2 years baby . last year on dec I had an abortion and today now my pregnancy is 5 weeks. this is my unplanned pregnancy so ,if I do abortion then does it affect my body and can cause any problem in future pregnancy? I am confused and don't know what to do .
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So a couple nights ago I drank and can't remember part of the night. The funny thing is usually when I get drunk a trip n fall and that type of stuff and remember it fine. I wasn't drunk enough to be doing that but the whole night is hazy. And I guess I tried to have a conversation with a buddy's mom and I don't remember it. The bad thing is there are thoughts and feelings I have that I hope I didn't tell her about and I'm afraid I did. I'm to chicken to ask. I kept on telling them I wasn't drunk. I also remember thinking this is my last beer and I'm done but I'm pretty sure I drank more after that. All the people that I was drinking with say I was very drunk. And I just can't remember. I know my drink wasn't spiked or anything. But I'm also told my husband wanted me to go to bed and I didn't want to don't remember that either. I did start drinking on an empty stomach. But then I ate after about 2 beers.
My question how to prevent future memory loss cause sometimes it happens sometimes it does. And why. And does anyone think I would have said embarrassing things to the buddy's mom
Ps I'm not an alchohalic And I'm of legal drinking age and a responsible adult 90 percent of the time
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My husband has hyperthyroidism and his taking Tapazole 5mg, We were planning on having a Baby but I'm afraid if his medication can affect the Baby..
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