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Pudendal Neuralgia/IBD/Nerve Injections

Anyone else been told they have this? A doctor poked at my nerves all day and my stomach ones are particularly sensitive. Sending signals all over the place, but apparently it's been bothering me my whole life, not just since UC and various surgeries.
I thought the UC diagnosis was the reason I had always been in so much pain in my life. But now it turns out I might have Crohn's as well. I'm in daily pain that's only getting worse since my cuffitis flare started.
I'm supposed to get nerve injections toward the end of May. I'm so sick of being on so many medications to manage the pain. Are there any brilliant moves I haven't been making for pain management ideas? Please help.
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