|
#102
●
05-24-2015, 10:59 PM
| ||||||||
 My Rank: LANCE CORPORAL Poster Rank:1836 Female Join Date: May 2009 Posts: 279 Mentioned: 0 Post(s) Quoted: 4 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
Voldemort looking' things.... Except that headless chicken one! That was humorous. God I will never try to have children. Ew.
|
|
#103
●
05-27-2015, 08:37 PM
| ||||||||
| My Rank: PRIVATE Poster Rank:6677 Female Join Date: Dec 2014 Posts: 32 Mentioned: 0 Post(s) Quoted: 8 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
Awesome contributions, thanks. Something about deformities that fascinate me in some morbid way.  |
|
#104
●
05-28-2015, 01:07 PM
| ||||||||
 My Rank: PRIVATE Poster Rank:7310 Female Join Date: May 2015 Posts: 27 Mentioned: 0 Post(s) Quoted: 5 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
here some deseases we can see on this interesting and extensive post: Harlequin ectiosis epidermolis bulosa hydrocephal baby anancephaly burned victimes 3 or 4 pics mermaid syndrome osteomalacia imperfecta Treacher collins syndrome goitre spina bifidas etc.  |
|
#105
●
05-28-2015, 04:08 PM
| ||||||||
 ★The Queen★ Poster Rank:67 Female Join Date: Jun 2011 Posts: 23,498
Contributions: 120
Mentioned: 95 Post(s) Quoted: 3083 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
Man With Rare Disfiguring Treacher Collins Syndrome Flies Across World To Meet Boy With Same Condition cdn.inquisitr.com November 26, 2014 Jono Lancaster, 30, was born with Treacher Collins Syndrome, a rare genetic disorder that affects about 1 in 50,000 people. Treacher Collins syndrome prevents the skull, cheekbones and jawbones from developing in a person. It also often results in a cleft palate, eye abnormalities that can lead to blindness, and in severe cases, the underdevelopment of the facial bones in a person with Treacher Collins syndrome can restrict the airway, causing life threatening respiratory problems. “People are lucky enough to win the lottery or they become professional footballers, doctors, lawyers but, I thought, ‘Why did I have to end up looking like this?'” Lancaster said. He admits that it took him more than 20 years to learn to love his own face, but now he wouldn’t change it for the world. In fact, he has dedicated his life to inspire others with Treacher Collins syndrome, and to teach them to love themselves for who they are. And so he flew to Australia earlier in November in order to meet 2 year old Zackary Walton, of Mannum, who also happens to have the same syndrome. “I grew up with Treacher Collins and I kind of felt like I was on my own and I felt like I was the only one out in the world that was like me,” Lancaster said — words that little Zackary will never have to repeat, now that he has met someone like himself. Lancaster added, “I would have loved to have met somebody like myself when I was younger… somebody who had got a job, got a partner and said to me, ‘these are the things you can do, you can achieve.'” Zackary made headlines in Australia when his mother, Sarah Walton, lost her government funding that provided her family with a nurse to help care for Zackary one day a week. Zackary requires a tracheotomy tube to keep him alive. Walton did have services for her son reinstated by the Australian government, and next year, when he is three, Zackary will undergo a number of operations at the Women’s and Children’s Australian Craniofacial Unit — including one procedure to break his jaw in the hopes that he can breathe more easily. It was Zackary’s mother, Sarah, who also contacted Jono on Facebook — Jono is the most famous person with Treacher Collins syndrome, and Sarah had hopes that her own son would meet him some day. “He, (Jono), is a celebrity to us — he’s a huge inspiration,” she said. “When he said he was coming to Australia, we knew we had to meet him and it’s made us so happy to see Zack meet someone like him.” Jono and his partner, Laura Richards, spent several days with Zackary Walton and his family. Photos Jono Lancaster and Zackary Walton Zackary with Sarah, his mother. [Images via www.adelaidenow.com]  ·  · |
|
#108
●
05-29-2015, 08:05 AM
| ||||||||
 ★ Legacy Member ★ Poster Rank:468 I am what I eat Join Date: Jul 2014 Posts: 2,299 Mentioned: 9 Post(s) Quoted: 1418 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
This is hands down one of my favorite threads. Thank you |
|
#110
●
05-29-2015, 11:17 AM
| ||||||||
 ★ Legacy Member ★ Poster Rank:569 Female last I looked Join Date: May 2015 Posts: 1,702 Mentioned: 14 Post(s) Quoted: 831 Post(s)
| ||||||||
|
Re: DEFORMED AND DIFFERENT - CHILD WARNING***
Ive seen a "mermaid" baby in real life. I was a photographer for a infant beravement nonprofit organization called Now I Lay Me Down To Sleep and one of my calls was to take pics of one. The parents just called her/him "baby" because without amnio fluid/blood testing there's no way to tell if it's a male or female. Cute baby, fused from waist down to the ankles then the ankles were fused together and the feet actually looked like flippers.
|
