PGAD - persistent genital arousal disorder

[Violet M]

I was trying to find studies that would support the use of neuromodulation for pudendal neuralgia or related problems but I'm not finding enough conclusive studies, unfortunately. I was also trying to think of other ways they could code your diagnosis that would have studies to support it but I'm not coming up with anything at the moment. Maybe your physician would have some ideas on how to code it differently so that studies would support neuromodulation. It's a tough situation you are in. Do you know if your insurance will cover surgery if you decide to go that route?

Violet

[nypain]

Thanks for trying! I may ask my pain management doctor, Dr. Kirpekar (who is lovely and has at least helped me explore a lot of options) to connect me with the neurostim rep - maybe the rep has ideas on how to appeal.

If I am offered and keep UHC next year, it might be covered. My other option is that I know of is Aetna, which definitely does not, unfortunately.

I may ask about amitryiptline in the interim, since some on this board report success, but I am afraid that if I gain significant weight from it, doctors will blame all of my problems on the weight.

[Violet M]

That's a good idea to ask the pain management doctor and the rep. Hopefully they will have some ideas for you.

I used lexapro (an SSRI antidepressant) for PGAD symptom relief because I couldn't tolerate the side effects of tricyclic antidepressants very well. It didn't take away the problem entirely but it dampened the symptoms. I titrated off of it slowly a little while after surgery. I don't like taking meds but sometimes they can help you get through a difficult time. It's kind of trial and error to find what works for each person. Hope you find something that helps.

Violet