Intimacy

Posted , 4 users are following.

Hello Everyone,

I really hate to ask this question, but is anyone feeling less intimate while taking the medications to treat the lupus (Plaquenil and Prednisone) ?

Lately I have not been feeling too sexual; it could be attributed to this condition or it could be coming from the fact that I am Peri-menopausal.

I can definitely say that I don't feel my old self; and I guess that includes being sexual.

Any feedback would be greatly appreciated.

Have a Great Day !

0 likes, 8 replies

8 Replies

  • Posted

    It is a very tricky subject. When I am having flare up the last thing I want is to be intimate with my hubby! Luckily he is very understanding.

    I dont think it is the tablets more the extreme fatigue that comes along with lupus.

    A tip that I have found is maybe try spending time in bed first thing in a morning rather than waiting until the evening! This when I find it is the last thing I feel like!

    I also tend to have an afternoon nap at  weekend and my hubby is more than happy to join me!

    Hope this helps a little and hopefully you will find your mojo!!!

    x

    • Posted

      Hi Katieo,

      Thanks for responding to my question.  I will try what you suggested.

  • Posted

    Hi,

    Some of the side effects of the meds could be to blame, but as Katieo says feeling like crap puts you off sex anyway!!

    I always put my lack of libido down to menopausal symptoms and then post-Hysterectomy pre-HRT dryness (OMG so sore, like glass cutting!!) but even with HRT I get sore and really don't feel like engaging in sex most of the time. I now use a non-hormonal moisturising gel in addition to the HRT which has helped. I take Hydroxychloroquine and Amitriptyline both of which have dryness as a side effect so may be they have contributed but I also have had episodes of gritty dry eyes and mouth long before being diagnosed with UCTD, so as you can see it's a bit of a conundrum!

    Honestly I think it's a bit of everything and now just smile, fantasise about Keanu Reeves and lubricate!

    Best of luck!

    • Posted

      Hi Susan,

      Thank you for information.  Willing to try anything....

    • Posted

      Hi, Tanya,

      Hope you find a way to get back to being able to enjoy all aspects of your life. Having an emotional and physical connection with your partner is so very important when you have a God-awful condition like Lupus or any of these autoimmune diseases.

      Best wishes.

    • Posted

      Hi Susan,

      Thank you so much for your words of inspiration.

      Best wishes to you as well..

  • Posted

    I agree with katieo, I is difficult. I usually lie on the bed in the afternoon, and again, we do lie in  on a morning. It does usually work.. Good luck..
  • Posted

    Hi tanya it probley is just the lupus flares really that put me off intimacy but im not old enough yet for menapause so i just assume its my illness that i have odd off days ... Never thought about meds being the couse which is likey too ..... But me n hubby try get breaks away just two of u just gives you that exiting feeling of fun ...

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