Ive Lost my 'MO JO'... sex problem :o(

Hi Anon,

It's not inevitable, but very common with MS, I'm afraid (in both sexes).

Have you recently had a relapse?  If you have, some, or most of the sensation may return.

With me, it took several months.  Luckily, I wasn't in a relationship, so for me it wasn't the highest priority, but I was aware of "not being right" in that respect.

I think I'm about 96 or 97% back to where I was - i.e, not perfect, but could perform, given the right circumstances... 

It's a shame it's not 100%, but then again, I'm almost 46 now, so it's probably unrealistic to compare with how I once was.  I expect some changes are natural, at my age, whether or not I had MS.

Tina

Hi anonymous. Sorry to hear of your problem, this illness robs us of enough without taking our sex lives too! 

You might want to look into purchasing an electric pelvic toning device, as they increase blood flow therefore increasing sensitivity, improve bladder issues no end, tighten up down there and - best of all in my opinion - make orgasm MUCH stronger! 

I have a kegel 8 and, obviously after the last bit above, I love it. I am much more sensitive and orgasmic since starting using it, and I need to pee less often too. They are not cheap but worth every penny.  

Hi Anon, I'm going anon as well, I seem to go between the two, hardly any feeling, and then too much, to the point of being uncomfortable, I've seen my GP because I thought I had thrush, but no, and my urine sample was negaive so she's says it could be nerve damage, great, hope you get things sorted, Love Anon x