Atrophic Vaginitis :: Depression, Anxiety And Confusion
Oct 25, 2015
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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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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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 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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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 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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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 was diagnosed with RRMS in 2000 in the middle of flare which caused numbness in my face and just a weird feeling when I walked. I have been fortunate not to have experienced too many problems aside from a couple of minor flares and the usual fatigue that goes along with MS.
Last week I was on my computer and all of a sudden I felt like I was not quite sure what was real...thoughts racing from one thing to another. I kept thinking of things and would immediately wonder if it happened. I finally decided to go the the ER. Doc did a neuro exam and said it was OK. I also thought I had a UTI but urine came back clear. He told me to go home and rest. The next morning when I talked to my daughter she said I sounded weird and it was taking me a long me to explain things. The MS nurse also said my speech seemed a little off and slow. Neurologist was out of town but when he came back he told her to call me to set up an EEG because it could have been a seizure. Since then my hand tremor has been more pronounced and weird little symptoms like twitches and sort of an internal tremor in my legs when I walk. I have the EEG next week and then will see my neuro.
I was just wondering else has had something similar. It was distressing to me because I can't really remember things I am usually right on top of; I couldn't remember my meds (I have a list at least). I felt like I lost time and was not sure how much.
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My physician hasn't been very helpful on the matter of brain fog. I can't focus. I am constantly losing my train of thought and half the time can not speak without sounding like I just had something along the lines of a stroke. I sometimes can't form a complete thought. I've had Fibromyalgia since I was a child and I'm used to the pain, it's just a part of my life now, but the fog seems to be worsening. It's hard to even write this because I keep losing track of the topic.
It's putting my job on the line. I can barely function. I'm feeling like I can't do anything right. I have a hard time processing what people are saying to me and everyone is so tired of having to repeat themselves, and people are always yelling at me for constantly forgetting things and it's like I'm in a constant state of confusion. It's like my brain is tired. I had to make a PA a while back to the customers at work and I had to have someone help me because I couldn't think, and I couldn't get the words out and I told them, very slowly, "help please make this PA, I can't do words right".
Before I forget what my point was, I'm asking if there's something that can be done, on my own. I'm barely functioning, and need some advice. My doctor wasn't very helpful at all, and he won't hear me out. He won't refer me to pain management because he wants to take care of this himself, which he isn't doing. He has me on Tramadol and while it helps take the pain from a 9 to a 4, it definitely makes the fibro fog worse.
Is anyone else dealing with this? What do you do to help it? I'm only 22 and I feel like fibro fog is going to destroy my future.
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I recently had outpatient gynecological surgery, following which I had frequent urination, burning, stinging when urinating and side and back pain on the right side. Went back to my doctor, and she diagnosed a UTI and put me on doxy and Cipro. Took them a few days, but the side and back pain persisted, on and off, in waves. I also became debilitated with extreme fatigue and weakness--i went back to the doctor, and couldn't even fill out a simple form in the office, simply couldn't think or have the energy to write. She sent me to the ER, saying she thought I had a kidney stone. They did a CT scan and said I have stone in my kidney, but that normally when it's in the kidney it doesn't cause pain. They couldn't explain my other symptoms (included also sweating, fairly frequent urination, low grade fever, confusion). They gave me 2 rounds of pain meds (& fluids) in the ER and I felt better for a couple hours. The next day I felt so rotten and weak I could barely sit up, i couldn't talk, check email or texts, read, move, shower, etc. over the past 3 days it has gotten slightly better. The pain has virtually subsided since the ER, but the fatigue is debilitating. Two friends described their experiences with kidney stones as similar--has anyone experienced the same? Does anything help?
I have heard water and beer help a kidney stone pass, but is that only once it's descended? I'm not really in pain, so my doctor thinks it may have shifted around in the kidney (she thinks my symptoms are something else). Anyway. I don't know if it would do any good to try to flush it out at this point or just wait and see. I simply can't go on for much longer feeling this extreme weakness and cloudy head, feeling rotten, etc. I continue to have a low grade fever, but my labs came back after the antibiotics clean. I do have similar symptoms when I get bad sinus infections, but that's clearly not the case now. Thanks!
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I've been on venlafaxine for about 2 years, taking a dose of 150 mg per day. I used to take the generic pills which are cheaper. To be honest I didn't even know there was an 'original' one, named Effexor, until last friday.
When I changed town I continued the treatment with another doctor, and he suggested i came off the drug. I thought I'd try, and for the first month I reduced from 150mg to 75mg. Nothing wrong there. Then I took another step and reduced from 75 to 37,5mg and in the fourth day I collapsed.
I had this breakdown, feeling all kind of weird symptoms: dizziness, dry mouth, excess sleepiness, confusion, mental oblivions (memory lapses), total apathy, total loss of libido.
I got really scared and tried to go back on my own since I was off town and couldn't talk to the doctor.
I took for 3 days the 150 mg pills but that didn't help. I consulted another doctor and he suggested to take a 107,5 mg dose (75+37,5) for 20 days and then restore the original 150 mg dose afterwards.
It's been 6 days since I started taking this dose and I still feel awful! I feel like I'm not the same anymore!!! It's the strangest thing ever. I had to ask for a job-absent license cause I can't work in these conditions.
One other thing is that a moved from the generic pills to the Effexor (from Pfizer - Wyeth) - the doc suggested that - and I don't know if that is making things worse...
I feel really awkward, useless, like my brain is in slow motion. I've been thinking about going' cold turkey since taking back venlafaxine did not help.
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I'm 17, I've been going through depression since about april last year. Stupidly i never got help until last week because it got really serious, i almost ended my life i constantly self-harm as it brings me a feeling i suppose?
Anyway i have been with my girlfriend since i was 16, first met her just after christmas. I bought her of loads of problems 'self-harm, low self-esteem etc.' it wasn't easy from the start because of her lod friends being bitches and she left them for me. My depression started in april when i become depressed and anxious about her leaving me because i felt inadequate as i was fro everyone i met. However we/I i got through it. Come to my birthday december 22nd.. I became ill and somehow really depressed i felt confused and unsure about my feelings for my girlfriend.. i became suicidal (btw i was this way in the months before but this was the worst case.) it came and went but for some reason since april this year stuck in my mind with my feelings for her. We argued/argue all the time about my depression or silly stuff. My summer was rubbish because of my depression. A few months ago i realised that i actually do love her. It made a little positive, we still met up in the week once and stayed almost every weekend, which i enjoy however we argued because i become down and sasd and negative and ruined everything. Fast forward to this month, she has almost broke up with me, because she can't handle my depression i almost left her a few times at the start of the year because i was so down and my mind was telling me allsorts. Anyway we are still together because we love each other and would like what happens after depression. My feelings are i worry/feel i don't like how she looks or dresses sometimes (she put weight on her face and has a double chin). My depressive thoughts were persistent and i told her i don't like her chin or hair sometimes. This created loads of problems i regret however i keep saying it. I feel like ending my life because i can't treat her this way. She is amazing and i feel i want to marry her and be the best i can for her but she deserves better and i just don't want to feel this way anymore i want everything i dream of when i'm positive.
I want to know if my thoughts are even true or irrational?
What could she do to help me?
And what can i do because i can't carry on feeling this way and lose that amazing women!
P.s I'm really sorry if it all seems weird and don't make sense i'm so upset and i didn't know to word or even make sense of what my minds doing to me. There is many things i'd like to say so please feel free to ask any questions about anything.
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