Unable to urinate, just trickle, trickle, going out of my mind with worry

Posted , 10 users are following.

Hi,

Has this ever happened to any one of you who had trouble urinating and was a bit constipated? I'm concerned especially about have trouble urinating. No matter how much I drink, it's just trickle, trickle. Has anyone experienced this problem and what you did to rectify it? I've had LS for 6 years and started using clob, premarin, and borax on off clob days. I've just been to the Vulva Clinic here but this was before I had this trouble. She said I should be concerned about my clitoris as there was a bit of white on it. Could this be the problem? I looked to see if the urethra is ok and it is open. There's nothing blocking it. Could the constipation be the cause. What an awful disease.

Micheline

0 likes, 48 replies

48 Replies

Next
  • Posted

    Maybe you have a Urinary tract infection. You should have your urine checked for infection. 
    • Posted

      I've had a Urinary Tract Infection before, and this doesn't feel like it. I have no pain. I seem to be constipated also. I saw a urologist and told her I had lichen sclerosis and I wanted to have things checked. She booked an appointment for me for January 18. I left a urine specimen and she said she would send it out to have it checked. I haven't heard anything. That was on October 23rd.

    • Posted

      I certainly would go to a different doctor. I would go to a urologist. I have both LS & bladder retention. 

    • Posted

      Hi Rona,

      Yes, I did go to a urologist. I had the cystoscopy my bladder and urethra are ok. There is no blockage. Was it a urologist who told you you had bladder retention. What's causing your bladder retention. I'm still searching. The doctor told me it could be a weak bladder.

  • Posted

    Sorry, never had that problem so I can't comment. Hope someone else can be of assistance

    chicks

  • Posted

    Hiya. You could have PFD. I have this an LS. Very annoying! X
    • Posted

      Thank you Claire for your response. I do have lichen sclerosis. Does this usually go with it?
    • Posted

      dont think usually but it can be a contributory factor. Any issue that causes pain in your undercarriage can make you unconsciously tense up which creates hypertonic muscles = PFD. 
    • Posted

      Meant to say, cos the muscles are extra tight it can affect the bladder and bowel making it difficult to go to the loo. 
    • Posted

      I think that probably enters into it also. Everything did feel very very tight -- I mean the back especially. I didn't think I was constipated because my stools were not hard, but I was all along. Also, it's like a vicious cycle. The more fear you have hence the stress and the tighter you get, the tighter you get and can't eliminate, the more fear and on and on in a circle. And believe me, that's what has gotten me here in the first place -- stress.

    • Posted

      Regarding your response Claire, I want to add something here. What really peeves me is when some of these doctors fail to instruct you properly or are aloof or arrogant. When I think of it now I get angry. When I went to the Vulva Clinic on Nov 2, I didn't have a urination retention problem. It's what she told me that got me worried. Here she tells me that I should be concerned about my clitoris. I just stared at her and got tongue-tied out of fear. Then she tells me that there's a bit of white on it. And that's it. That's all she told me when she walked out of the room. She didn't tell me what to do about it and gave me an appointment for Nov 2, 2018. I remember coming home and couldn't stop thinking about that and then I started worrying about it. I'm a natural worry-wort anyway. And then, I started having trouble urinating. It's amazing though how subtle the tenseness that evolves from the fear and worry happens and gradually tightens everything, all the muscles. I was not even aware of it. Yes, I knew I was tight but wasn't really aware what caused it. Thanks for enlightening me about it  Doctors are supposed to make you well, not make you worry!

    • Posted

      Some doctors are good but in my experience you will get much better advice from your fellow sufferers. If you are on Facebook you can join some fantastic forum groups for LS and PFD. 
    • Posted

      Well I wish I could find the good ones. They are very few it looks like and where are the ones that have good knowledge about this dreadful disease? And that's why I joined this wonderful group here some time ago. The people here helped me before on this forum and I thank them wholeheartedly. I don't know about Facebook. I am on Facebook but I don't know if I can trust it's privacy, but thanks for the suggestion. I'll look up their advice though.     

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.