Please login or register.

Login with username, password and session length
Advanced search  

News:

Got a story to tell for the magazine? Get in touch with the editor!

media

Pages: 1 [2] 3

Author Topic: Burning Urethra  (Read 28218 times)

Hattie

  • Guest
Re: Burning Urethra
« Reply #15 on: September 23, 2014, 01:01:59 PM »

So kind of you all to reply. What a wonderful site this is. Yes, last year I had treatment for Pudendal neuralgia

Midnight Shadow

Could i ask you please for the name of the physio that you saw - i am assuming that you are in the UK.

If you do not want to put a name on the forum i could send you my email by personal message on here.

As a new member you may be able to Personal message me as you have now done 10 posts but i am not entirely sure about that. Just click on my name and send a pm should come up

Thank you for your trouble if you are able to.

Hattie X
« Last Edit: September 23, 2014, 03:37:38 PM by Hattie »
Logged

Maryjane

  • Member
  • *
  • Posts: 1612
Re: Burning Urethra
« Reply #16 on: September 23, 2014, 01:16:09 PM »

Hi Midnight Shadow, I would be going back to your physio asap as I wouldn't be surprised if your PN isn't raising its ugly head again, the more we go into meno if we have this problem the more it needs to be nursed as once you have it, it is like an old back injury etc.

I started off two years ago after having polyps removed from my womb, with a burning urethra when I pd, backwards and forwards to gp,local Uro/gynae etc didn't get any better, so started my journey cut a very long story short I have PN which is seen more often in menopausal women than is realised but is misdiagnosed.

I then went to see a Uro/gyna and I have e-coli with a thickened bladder of 7mm this is extremely thick it should be about 3.5mm, so I have been on ten weeks of rotational antibs, saw the consultant six weeks ago and it had gone down to 2.5mm even he was amazed, but I still had infection, so had another four weeks of antibs.

 I now know which antib got rid of the infection and it was Nitroformin (sp), as I changed after two weeks to ciprofloxin and within four daysi was in quite a lot of pain again, I have been off the antibs for two weeks now, I tested my p yesterday and I have, blood +2 , leukocytes off the scale plus nitrates and a touch of protein, so it is looking like my infection is back.

Slightly going off track but my dog had exactly the same problem, three months of antibs and half her bladder removed because the infection had done so much damage, incidentally caused when she was spade, they see it quite often ( far more than they let on). She had formed pockets in her bladder where infection lived.

Back to humans, I have not been on antibs for 25+years or any form of medication and I hate being on it, however my infection obviously has taken a hold and has formed these pockets of infection, long term untreated UTIS can cause untold nerve damage as Judith 57 and myself have found out to our cost.

Two days of antibs and my pain reduces dramatically, I am very aware of the long term use of antibs ( daughters a vet ) however I can't do right for doing wrong in this situation, I just hope my lack of having them over the years helps, grasping at straws here, but I get checked every month for thrush, and so far none and my PH level is spot on, some people never get thrush however long they are on antibs.

I also wake up pain free and don't start getting uncomfortable until about 2.00pm, I have been told by three eminent specialists that this is the nerve/nerves firing off as the day progresses, if I lie down and put my feet up above my head the pain generally goes within ten minutes.

I am also on cimetidene as this has antinflamatorie in 70% of patients, with blader pain. Painfull blader syndrome/IC does not respond to antibs, and there is a high chance I will be left with this after the 18 months of undiagnosed UTIS.

I was given steroid cream burnt like crazy, you can ask to have it made into an ointment which does not have all the additives added, as they will be what you are reacting to, but I just use actigel (same as honeybun, can't remeber proper name), and the yes oil based stuff, if you touch the end of urethra does it hurt? Mine did I went through the roof the first thing to stop hurting after I started the antibs was that, however it's all flipping back now. :'(

I am going to try local oestrogen again, to see if that helps they are not keen on me having the oestring as they don't want anything left up there.

I have given up all wheat/gluten/dairy and processed sugars, and just eat pears as these are the only bladder friendly fruits, since giving up these items my energy has really really increased, and my IBS bloating/wind has gone. I drink coconut milk, and coconut yogurts which have a soothing effect, they say about bladder pain/urethrea that if you where to have an open wound on your hand, would you squeeze a fresh orange on it etc no because it will sting , but you would put milk, porridge etc on it the same for our bladder regards what we eat and drink.

I have also stopped eating any of the low fat items, especially spreads as they are one chemical away from plastic and full of sugar, back to good old butter, as butter doesn't come under dairy can't remember why.





Logged

Dancinggirl

  • Member
  • *
  • Posts: 7091
Re: Burning Urethra
« Reply #17 on: September 23, 2014, 02:03:26 PM »

Maryjane - very interesting post. My burning urethra has been helped by local oestrogen - I'm really worried they are going to, one day, say I have to stop using it.  I was interested by the comment about the pain starting after the middle of the day because of nerves firing off - that makes a lot of sense and would explain why things are less painful at night as well.
I've never had a urine test that has come back showing any kind of infection, only blood. The urologist said I probably had scar tissue in my urethra which is causing the bleeding and pain (the cystoscopy showed a healthy bladder wall)   - he told me to come back if the local oestrogen didn't help. While I was on systemic HRT the burning was only sporadic and not as bad as when I first came off HRT last autumn.
I had a premature meno (from mid 30s) and I think I was on too low a dose of oestrogen to keep may bladder etc. healthy - my burning started when I was about 43 when I must have gone into post meno and I was only using one pump of oestrogen per day.
I have tried changing my diet - leaving out all the usually suspects  - the only things that seem to irritate are citrus so I continue to avoid these and allow myself only the occasional cup of tea as a treat. I work for a brewery and strangely beer doesn't seem to irritate - though I only drink an occasional slurp now and again. Unfortunately alcohol gives me a headache now I'm off HRT.  Menopause doesn't half spoil all the fun!! :'(
DG x
Logged

Hattie

  • Guest
Re: Burning Urethra
« Reply #18 on: September 23, 2014, 05:10:46 PM »

 :hug:  Maryjane
Logged

Midnight Shadow

  • Member
  • *
  • Posts: 350
Re: Burning Urethra
« Reply #19 on: September 23, 2014, 05:44:25 PM »

Just returned from my doctors as the burning was horrendous today. :'( Saw our practice nurse who is extremely knowledgeable and she has prescribed a cream called Timetodine, apparently it is an anaesthetic, barrier and steroid cream all in one. Have only used it once, so I will let you know how I get on with it. Burns a little at first, but I think anything used in our delicate area burns.  She did say that our conditions are extremely common and definitely made worse by sitting all day.  Love coming home and sitting in a salt bath, very soothing. Hope we can all get sorted very soon.  :)
Logged

Judith57

  • Member
  • *
  • Posts: 315
Re: Burning Urethra
« Reply #20 on: September 23, 2014, 06:12:40 PM »

Hattie, MJ and anyone else that may be interested I see that our previous thread has now been renamed pelvic pain.

Midnight Shadow, I too would be interested in knowing the name of the amazing physio who helped you.
Logged

Maryjane

  • Member
  • *
  • Posts: 1612
Re: Burning Urethra
« Reply #21 on: September 23, 2014, 06:28:48 PM »

Me to re physio, I believe you live in London ? I know of two with very good names there I go to one of them. Off to London again tomorrow to Uro/gynae.

I was out walking across the fields this am, really fast walk hour and a half got myself sweating and puffing, no aches and pains worth noting elsewhere in my body and I still find it almost unbelievable that I am broken due to my vagina.

I work for myself and had a client come and see me tonight, saying I can't sit because of my back if I told them the truth I think they would run for the hills. ;D
Logged

Maryjane

  • Member
  • *
  • Posts: 1612
Re: Burning Urethra
« Reply #22 on: September 23, 2014, 06:41:36 PM »

Hi Moonlight I will ask about that cream, it's sounds very similar to what I was given " trimovate" which is a 3xcombination like yours, I had to stop using it as made the burn worse and the dermo I saw told me it is off license for the vulva area so just check, one of the ingredients in mine was just to strong for that area.

I don't suffer as bad as you and J57 because I don't sit for along time, probably no more than thirty mins, but I can sit up to two hours if I sit in perfect posture and do not slouch.


Logged

Midnight Shadow

  • Member
  • *
  • Posts: 350
Re: Burning Urethra
« Reply #23 on: September 23, 2014, 07:14:13 PM »

My new cream should have said Timodine. Sorry about that.  :)
Logged

Hattie

  • Guest
Re: Burning Urethra
« Reply #24 on: September 23, 2014, 07:49:20 PM »

Midnight Shadow

i've had Timodine in the past for thrush as it contains nystatin.

Quite like your other name for it  ;D  as isn't it a cream that you store in the fridge ?

Hattie X
Logged

Dancinggirl

  • Member
  • *
  • Posts: 7091
Re: Burning Urethra
« Reply #25 on: September 23, 2014, 08:11:19 PM »

I've got a bit of a low grade virus at the moment  - feeling achy and really tired - so I lay down on the sofa for half an hour this afternoon and the burning was definitely better. I also find my urethra burns far less in the evening after I have had my dinner - I'm wondering if low blood sugar has something to do with things?!!!
I think sitting in a supportive chair that encourages good posture does reduce the burning.  I have a very old Lloyd Loom chair (falling to pieces unfortunately) that I find so comfortable and the wicker allows some air circulation to the nether regions. My husband has a bad back and he finds that chair very supportive as well.
  DG x
Logged

Hattie

  • Guest
Re: Burning Urethra
« Reply #26 on: September 25, 2014, 10:31:45 AM »

Midnight Shadow   

Please could i ask you again for the name of the physio you saw last year who cleared your pudendal neuralgia.

Could you just please post back here on this thread if you are able to and i will send a personal message to you with my email.

Thank you if you can   :thankyou:

These physios are like golddust and most of us have to travel a distance to see one.

Hattie X
Logged

Midnight Shadow

  • Member
  • *
  • Posts: 350
Re: Burning Urethra
« Reply #27 on: September 25, 2014, 05:39:59 PM »

Regarding my physio Hattie, do you live anywhere near Grantham Lincolnshire?
Logged

Hattie

  • Guest
Re: Burning Urethra
« Reply #28 on: September 25, 2014, 06:24:02 PM »

Midnight Shadow

Unfortunately not but two other ladies are interested on here if you are still willing to let me have a name.

Many UK people are looking on the Hope forum (which is mainly USA) as well for a physio who is capable of helping PN.

I apologise for jumping on you with this when you are just a new member to the forum   :) 

Hattie X
« Last Edit: September 25, 2014, 06:37:07 PM by Hattie »
Logged

Midnight Shadow

  • Member
  • *
  • Posts: 350
Re: Burning Urethra
« Reply #29 on: September 25, 2014, 06:42:01 PM »

 No problem Hattie. No I didn't have internal physio for my Pudendal Neuralgia. It was just a gentle massage on the pubic bone area. I didn't have any burning at that time just a toothache like pain. My treatment then was really posture based.  It was completely different to what I am currently suffering. Having had the Trimodine cream for 2 days and used it as instructed 3 times daily I have been slightly better, not burning as much. Only hope it continues. I visit my physio on Monday, so will let you know how I get on and what she says about the possible burning being related to Pudendal Neuralgia.  ::)
Logged
Pages: 1 [2] 3