Cured from vulvodynia thanks to a fantastic team... but with some decidedly misplaced advice. Anyone like me?
Hi everyone, I wanted to share an aspect of my recovery from vulvodynia that's been bothering me for some time, and whether it's a common phenomenon. I want to make an important premise: the team of doctors who treated me (especially my pelvic physiotherapist and myofascial release physiotherapist) were absolutely fantastic. They were competent, compassionate, and thanks to their therapeutic journey, today, a year later, I can say I'm happily pain-free.
However, there was one sour note they kept repeating to me during sessions: they told me to "find a steady boyfriend," and that if I found one, I'd resolve the problem much more quickly and achieve stable results. In hindsight, I find this advice completely misplaced and the product of an outdated medical mentality that views a woman's body as a function of penetrative sex or traditional heterosexual relationships. The overwhelming proof? After recovering and finally freeing my body from neuropathic pain, I realized I'm asexual. I'm fine as I am, I don't feel the need for intercourse, and my physical stability is perfect even without a partner or forced stimulation. I didn't need a man to heal, I just needed adequate medical care.
Have any of you ever received this kind of relational/sexual "prescription" from therapists? I'd also love to talk to other women who, just like me, identify as asexual (or on the asexual spectrum) after recovering from or dealing with vulvodynia. How have you experienced your relationship with therapy and your doctors?