Added: 8 months ago
From: TheJonRisinger
Views: 407
Sort by time | Sort by thread (beta)

Link to this comment:

Share to:

All Comments (14)

Sign In or Sign Up now to post a comment!
  • Hey, i'm 16 and am in the same situation that you were!

    I got my first stimulation test at my endocrinologist last week and get results next!

    Kallmann is definitely a chance at this point, so we'll see what happens!

    Thanks for showing me that it will work out!

  • The injections aren't weren't working for me lol. I'm 17 and look 10.

  • KS meets comedy, good presentation young sir. You're lucky in that your treatment seems to have worked well for you giving you near normal development. Many of us are not that lucky. Treatment did a little for me but not 'the full works'.

  • This cracked me up and i have KS as well, good stuff man. i guess we learn to deal with it.

  • dude, you have kallmann? im from singapore and i have kallmann as well, just 1 quick question if you are reading this, are you still taking you injections regularly? and if so how do you over calm the part where you have to stab yourself twice a week? and do you have upper body numbness? i im getting numbness in the chest face and hands.

  • I am wondering if I have Kallman syndrome because people ALWAYS say I look way younger than I am. They say I look 13 or 14 and I am 18. I don't know what to do it has made me lose all my self astem. I can't grow facial hair and i don't have normal mucle development for someone of my age. What do I do? My parents ignore everything I say and say my hormone/testosterone levels are fine but that can't be true and I know it.

  • @madhatter534 ask your doctor, get a blood test, see a specialist. You won't know unless find out from an expert.

  • Hey dude, I need you to e-mail ASAP. I have KS as well, and there's a huge opportunity that I need to speak with you about. Please, at your earliest convenience: j_sholomith1@salemstate.edu

    You seem quite knowledgeable on KS, and you're able to make great light of it. What we need to talk about, in my opinion, is a huge opportunity...Perhaps once in a lifetime.

  • @johnpsho14 i happen to have KS too, my doctor told me that KS is very rare...

  • very informative and thats all i have to say about that!

  • @NZSCA

    i thought they said colemans syndrome too

    excellent video style

  • You still look like a college student. ;)

Loading...
Alert icon
0 / 00Unsaved Playlist Return to active list
    1. Your queue is empty. Add videos to your queue using this button:
      or sign in to load a different list.
    Loading...Loading...Saving...
    • Clear all videos from this list
    • Learn more