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Can people with Kallmann Syndrome work? What kind of work can they perform?

See how people with experience in Kallmann Syndrome give their opinion about whether people with Kallmann Syndrome can work and what kind of jobs are more appropriated for people with Kallmann Syndrome

Kallmann Syndrome jobs
8 answers
Yes they can work, could do pretty much any job. the only limit would be if you need to use your nose which doesnt actually work if you have Kallman syndrome

Posted Feb 22, 2017 by Alessio 150
Unless you have Oestyoperosis (Brittle Bones) it is possible to follow any career path you choose.

Posted Feb 22, 2017 by Kelly 1000
I do not think there is any limitation. The lack of sense of smell might be in an issue in some professions and the need to take weekly or fortnightly testosterone shots could be a problem in the military but requirements vary around the world.

Posted Feb 22, 2017 by Neil Smith 4395
Yes, cannot work with companies that require you to smell. Difficulties working in a daycare setting.

Posted Mar 10, 2017 by Miriam 1050
Every kind of work,

Posted Jun 11, 2017 by Remo 2050
I work in the US Coast Guard Auxiliary and I am the only known person with Kallmann's Syndrome in the US Military

Posted Aug 4, 2017 by Nick K.D Chaleunphone 1770
Any and all work. Having kallmann does not effect your career . In most cases you just don't have the ability to smell.

Posted Oct 10, 2017 by Megan 400
People with Kallmann Sydrome can do anything anyone else can, especially with hormone treatment. Military service may be restricted.

Posted Dec 1, 2017 by Aaron Davis 4150

Kallmann Syndrome jobs

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World map of Kallmann Syndrome

Find people with Kallmann Syndrome through the map. Connect with them and share experiences. Join the Kallmann Syndrome community.

Stories of Kallmann Syndrome

KALLMANN SYNDROME STORIES
Kallmann Syndrome stories
What can you say my story of how I was born as an http://en.wikipedia.org/wiki/Intersex/DSD person and living my life is as unique as the next person. I’m no different from anyone else, other than being born with an Intersex/ DSD (http://en.wikipe...
Kallmann Syndrome stories
My name is Ivan. I'm a clinical psychologist. I'm 40 years old and I have Kallman's syndrome. Unfortunately, it was diagnosed only a couple of years ago (in 2009).  My first 36 years of life without the diagnosis were not so bad, however, I develo...
Kallmann Syndrome stories
Short version to start with..... Born in 1969. Went to Bradford University to study Biomedical Sciences Was dismissed as a "late bloomer" or "late starter" every time I went to the doctor throughout my teenage years. Diagnosed at 23 at Royal ...
Kallmann Syndrome stories
When I was little and found out my Syndrome was a confused time, how doctors told me what my life will be and how could I live when been a grown up person. Now that I am 40 and knowing people that been there like me and talk about our story I can say...
Kallmann Syndrome stories
I have a Portuguese blog where I talked about my syndrome and my desire to become mom.  Is called https://cantinhodossmurfs.wordpress.com

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Kallmann Syndrome forum

KALLMANN SYNDROME FORUM
Kallmann Syndrome forum
We are currently seeking research participants who have been diagnosed with idiopathic hypogonadotropic hypogonadism (IHH), including Kallmann Syndrome (KS), for such a study.  This study is being run through the Pennsylvania State University De...

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