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Any success with female Kallmann's Syndrome?

I am a newbie here but I was diagnosed with Kallmanns Syndrome at age 17, now 29. It is very rare, and even more rare in females and I would love to talk to someone who is going through treatment or has been through this. Kallmanns syndrome is delayed puberty, no AF without medication, anovulation and no sense of smell. We are on our 5th round of injectables which has been VERY slow, and not super successful. We will probably be discussing other options after this cycle but my insurance won't cover IVF so it's not really an option right now. 
thanks in advance!
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