Ana Rodarte was born with neurofibromatosis, which caused tumors to cover half her face. She was in her twenties when a team of doctors led by plastic surgeon Munish Batra performed a series of operations that transformed her life. A journalist followed the process and wrote about how Rodarte's affliction shaped her world. Her email correspondence is included.
Link to part one. Link to part two. Link to photos. -via Digg
"i don't want kids no, the risk is too high for me to have them be born with the same condition. . . . i wouldn't want them having to experience what i did, and i cannot work, no one will hire me so i gave up on that, and i don't plan on ever getting married, i don't believe in it."
Of course she claimed she didn't care. "Not all dreams come true," she wrote once, sounding more resigned than bitter.
In time I interpreted her rationalizations as a measure of how vulnerable she was to the truth: that she would never be married, never gaze upon her own child or be anything less than dependent on others for her livelihood, and all because of her face. I wondered if someday she would prove me wrong.
Link to part one. Link to part two. Link to photos. -via Digg
The diagnosing doctor told him when he was 10 years of age that he had this insidious disease, and didn't give his mom the chance to explain it to him. He just blurted it out, and started rapidly commenting that he should never get married, never have children, that it was fatal and ugly.... My friend was so shocked, she couldn't speak. She regrets that incident, regrets that she could not protect him from the brutality of how it happened. He was deeply impacted for the rest of his life, like this young lady. They never expected him to live past his teens, but he lived until his mid 20s.
He did not have much of a social life, and was home-schooled during his middle-school years. He would have liked to take college courses, but was unable to do so as he started to go blind, and lost an eye - it had to be removed. He continued to drive until the other eye began to fail him. He refused to sell his car, though. It was precious to him, as a symbol of his lost freedom and independence, and he held onto that memory with all he had. He got weaker and weaker, and more and more tumors grew, marring his face. When his father died unexpectedly, and he could not even attend the funeral because he was in a rehab center, recovering from his fourth or fifth brain surgery.
Finally, the doctors told his mom that there would be no more surgeries, because the condition had advanced so far that there was nothing more they could do but make him comfortable and curse time while waiting for him to pass. She took him home, and they cared for one another as days turned into weeks. He continued to lose sight in his remaining eye, until he went blind. He lost weight. He lost neurological strength. He couldn't walk anymore, and his hands couldn't grip. His memory started to go. Finally, one night, he left this world in his sleep. When she went to wake him for breakfast, he was gone.
This young man had amazing strength and deep warmth and a wild sense of humor. I enjoyed being with him, sharing time with him, laughing with him and learning from him.
There are many "beautiful people" in life, but they may have "perfect" bodies and ugly souls. They are greedy, dishonest, selfish, malicious, unkind people. This young man - he didn't look like the rest of us "typical" folks - but he was more beautiful inside than they ever could hope to be. He may have looked different, even "ugly" to those who didn't understand, but he was still a human being. You could touch him, hug him, kiss him... it was okay... you couldn't "catch" anything... NF-II is not contageous. He was worth knowing. He was buried with his grandmother, and his mother aches for him every day. They were best friends.
So please, folks. Become informed. Be educated. Don't be afraid or disgusted by folks with this disease. Although passed genetically, sometimes it is a mutation - a "hiccup" - which causes the disease, as was the situation with my friend. Neither she nor her husband were carriers, yet her son was born with it.
Read the site below, and consider making a donation:
http://www.ctf.org/how-you-can-help/
Thanks for your time.
How would you feel if someone said they get "physical pain" from looking at your picture, and would feel offense if someone didn't warn them prior to showing it?
And yet that's something she deals with ALL the time, and you stupidly add to that without needing to.
Now, not only does she have to worry about reactions from people who actually see her, but she has to worry about idiotic reactions from people who have only seen a blurred picture of her.
and thank you so very much to the poster for not showing a picture, rather a blurry idea of her, because as sad the story is, i would not be able to read that, im so squeamish and it bugs me when blogs put pictures like that with no warning... i get physical pain from seeing stuff like that:/