Does Alcohol Make Anemia Symptoms Worse?

The other day (Sunday) I did something stupid and had a few beers (about 2 pints). Yesterday and today I noticed my symptoms have gotten a bit worse. Does alcohol make anemia symptoms worse?

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Ulcerative Colitis :: Salofalk Enemas Seem To Make Symptoms Worse

My son had a colonoscopy and told may have Colitis..he was prescribed a month's supply of Salofalk enemas and took first one last night...but today he has had to poop about 7 times with some blood ...the frequency of the pooping is now more than it was before using the Salofalk and I'm wondering has anyone else experienced this...he is only 18 and afraid to leave the house..It is not diarrhea but it's just he needs to go so often...I am afraid he will loose a lot of weight...If this is normal using this product I can relax...can someone please reassure me

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Alcohol :: Liver Damage After A Year Of Binge Drinking? Strange Symptoms

I know I suffer from anxiety (and depression and insomnia), which is partly what drove me to drink, am on treatment for same and will review things with my GP asap, but I want to concentrate on my physical health concerns.  Please ignore this thread if you ONLY want to talk about anxiety.

Briefly: I was a social drinker for 25 years, occasionally drinking more than I should have (but at things like celebrations and functions).

Two years ago, I began to develop mental health problems, but didn't start drinking more heavily (self-medicating) until about one year ago, when I also started to binge drink occasionally, including twice last October.  After a gap, I then restarted drinking heavily in March this year, and this became very heavy at times in the summer (80+ units per week), with occasional even heavier binges, the most recent being last Thursday / Friday (50+ units each day).

I finally ended-up in hospital last weekend with tachycardia, low blood pressure and probably alcohol poisoning.  While there, I first developed a painful red/purple rash on my chest.  I was put on antibiotics for this, and it seems to be clearing-up.

However, then, I quickly developed various other strange and unpleasant physical symptoms:

- numerous bruises;

- numerous pimples and red/purple dots under the skin;

- some hair loss and extensive hair-thinning;

- a spider naevus;

- red palms;

- itchy skin- skin darkening affecting the backs of my hands and genitals;

- regular, profuse sweating;

- whites of eyes turned lemon;

- brain "fog".

Some of these symptoms have reduced or resolved (eg. red palms and itchy skin), but the others have persisted.

I am eating OK, but making an effort to do so.  In spite of this, I have lost about a stone in weight in the past 3 weeks.  I'm also lacking in energy.

Since June, I have had regular liver function tests and other blood tests, too.

These have shown elevated enzymes, more or less in line with the extent of my drinking.  In early August, after a serious binge, the AST was 96 and GGT was 121.  In mid-August, AST had reduced to 25 and GGT 72.  But they were higher again (though both under 100) on my admission to hospital last weekend, but had started to fall again after I was there for a few days.  I have been advised that, in all of the tests, the values for other important measures were consistently normal.  The junior doctor in hospital said the LFTs indicated no cirrhosis or hepatitis. 

I also had a physical exam (just manual) from a GP in mid-August, and she said my liver / abdomen felt soft and suple with no sign of inflammation, enlargement or hardness.

However, given the strange and unpleasant physical symptoms that quickly developed in hospital last weekend, I fear that my last serious binge a week ago finally tipped me over the edge and into serious liver disease.  Too many of the symptoms are those of cirrhosis for me to think anything else.  (I've checked on the NHS website.)

I am absolutely terrified that, despite good advice and warnings, I did not take heed and my body, especially the liver, has finally been permanently damaged by the alcohol.

My main question is: can I turn things around?  I have not had anything to drink since last Friday, and have no inclination to do so.  I am drinking a lot of water, fruit and vegetable juices, and eating healthily.  I will try to get some exercise, though I don't have much energy.

I'll see my regular GP next week, but could do with some advice and, if it's appropriate, some reassurance before then.

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Atrophic Vaginitis :: Suppositories

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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Atrophic Vaginitis :: HRT - Success Or Failure?

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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Future Of Atrophic Vaginitis For Five Years?

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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Atrophic Vaginitis :: Tea Tree Suppositories

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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Atrophic Vaginitis :: Use Of Vagifem To Treat VA?

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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Atrophic Vaginitis :: How Do You Deal With The Anxiety - HRT?

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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Atrophic Vaginitis :: Thrush After Starting Vagifem

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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Atrophic Vaginitis :: Depression, Anxiety And Confusion

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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Atrophic Vaginitis :: Postmenopausal Burning And Itching In Vagina

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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Atrophic Vaginitis :: Mona Lisa's Smile Treatment

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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Atrophic Vaginitis? Mild Discharge, Burning And Itching

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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Atrophic Vaginitis :: Vitamin E Capsules And Gelatin Shell

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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Atrophic Vaginitis :: Spotting - Constant Burning, Abdominal Discomfort

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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Atrophic Vaginitis :: Vitamin E Suppositories In Treating The Dryness In The Vagina?

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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Atrophic Vaginitis :: Chemicals In Toilet Paper - Irritating To The Vulva?

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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Alzheimers :: Antidepressants Make You Worse

My grandfather is taking one and he is becoming way worse and just lays in bed all day and doesn't eat anything at all. And looks like he''s going to die soon. Only reason why I'm asking this question here too is because he has Alzheimer's too.

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