In class, we spoke about the Age of Gonads, followed by intersex and determining the sex of intersex children. This lead our discussion to the topic of the Intersex Society of North America. This site highlights intersex issues, and actions families may take to directly deal with their situation at hand.

After briefly talking about this site in class, I decided to follow-up this discussion by analyzing the site in order to answer questions of curiosity that occurred to me during our discussion. I found this site to be nothing but helpful, educating, and more than anything calming to those that may be dealing with an intersex situation. I found that all questions that I had about intersex were on the site with helpful solutions. A few specific questions I thought of are: What is intersex? How common is intersex? What do doctors do now when they encounter a child with intersex?

I clicked on all of these links on the side and after reading all the pages, I felt fully educated on the subject. For example, when explaining what intersex is, it gave the definition of intersex which is: “a general term used for a variety of conditions in which a person is born with a reproductive or sexual anatomy that doesn’t seem to fit the typical definitions of female or male.” It then continued to give an example of what this may mean stating that a person may look female on the exterior, but really internally they have male-typical anatomy. It also continued to explain that intersex is an inborn condition but is not always visible at birth.  I found this tab the most educating as it was the one that explained intersex and broke it down so that anybody could interpret it. It was also soothing for the INSA to state that they are open and caring and are trying to create a world free of shame, secrecy, and unwanted genital surgeries.

Next how common is intersex? The site began to breakdown the different types of intersex births followed by the probability that one would be intersex. For example, For Not xx and Not XY it said one in 1,666 births. This among many other variations is what this page consisted of.  It was based off of statics from Brown University researcher Anne Fausto-Sterling. In my eyes this page was important to include because it shows research and evidence of the rarity of the case, yet the possibility t at it can happen and if it does, it is okay.

Lastly, What do doctors do now when they encounter a patient with intersex? It states that doctors are willing to “cut now and worry about the quality of life later.” This is important, because the whole purpose of this site is to not just go ahead and do that. There is not much information or writing on this page as they state their concern and drive to implement their patient-centered model of care through visits to medical centers. Hopefully, this makes a difference for intersex people as it should be their decision.

This site fights for freedom of the intersex patients and is nothing but education and supportive to those that have this diagnosis. It gives these people hope and knowledge when dealing with their situation so they are able to make the best decision in what they want to do regarding their sex. This site is helpful, and whoever started it is a very smart person, as they have helped many people.

-C. Praljak