Normally when you are diagnosed with Klinefelters Syndrome, your first port of call is with the NHS system (UK). Endocrinologists that specialise in KS within the NHS are few and far between. They tend to be diabetes endo’s which cover hormone conditions.
This means they know some of the issues of KS and the standing joke is that we, as “sufferers” of KS tend to know more about our condition than any group of endos ever could. If you have read my other posts on this website, you will see that since my diagnosis in 2015 I have had 6 endo’s and I am currently without one at all.
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