For me it started a few years ago that I lost all interest in sex. At first it was pain from having had endo for nearly 20 years, then I had a hysterectomy in 2005 and started hormone replacement therapy. Since then, things have gotten worse. With each year it seems to get worse. Since earlier this year I haven't been able to even feel comfortable 'doing it'. My husband is a very patient man and loves me, bless him for that. I recently read that the inability to achieve orgasm or even feel sexually aroused can be due to MS. Is this true? Is anybody else 'suffering' from this? If so, how are you handling this?
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