If there are any other men out there who have been diagnosed with Kallmans Syndrome as myself, left with usual results of having very small genitals and the inability to develope much muscle mass, I would sure like to hear from you. You may be feeling as isolated as I did with this disorder, not to mention feeling like a guinea pig with so many tests and treatments. It is so important that we get together here and help support and inform eachother. The ultimate would be to get the medical profession to connect here also and assist to develop a KS Society, giving us a voice and a better awareness of ourselves and our lives with KS. AJ

Welcome to all.