I hope the people who say they shouldn't be together don't find love and happiness.
I wish more people in the world were like you - looks should be so unimportant in the grand scheme of things! The work you've done is absolutely superb, and your triumph through life's adversities is a total inspiration to everyone, no matter who they are or what they're going through. That decision has to be a personal one made by the two of you and you should feel no guilt whichever path you choose. Thank you for subscribing to our Push Notifications, Instantly get the most heartwarming & meaningful stories. Wishing you both the best of luck, your an inspriation! Read more. You are such a brave, kind and thoughtful person and whatever decision you and Laura come to will be the right one for you which is all that matters. In tonights programme you talked about the unkind comments people have made, that made me feel very sad and cross, one day I pray that all this ignorance will be a thing of the past. It can be heart breaking watching children suffer, especially if they have life threatening conditions. Complain about this comment (Comment number 65), Jono I think you are amazing and a truly beautiful human being, more people should be like you and I think it is a fantastic job you are doing, making people aware of your condition, particularly young children. Carry on ignoring those who put you down.. You come across as a really strong couple who will make amazing parents, if not more so because of all the thought and planning that has gone into making your decision. I hope to see you on tv again in the near future when the time is right for you and laura with news of your family, I truely wish you and Laura a long and happy future together x, Complain about this comment (Comment number 59). Dear Jono,I am watching your documentary and am wowed by what an amazing person you are. Thank you for sharing your life you lifted my spirits.
Join us as media missionaries! I wish you all the luck in the world and look forward to your next programme x, Complain about this comment (Comment number 38), I wanted to say I completely understand why you feel you're disrespecting people who already exist with genetic conditions and how that's an emotional issue for you. I think whatever you choose to do is your decision and you have shown that you have put an awful lot of consideration into it. The Heart Of A Champion: Boy Born With No Legs Pursues Baseball Dreams. I would like to say Jono, that I think that you are truly are an amazing person and think that you have a wonderful girlfriend, you will make great parents. Complain about this comment (Comment number 60). Jono and Laura - you are truly amazing, and I feel privileged to have been allowed a peek into your lives. Take no notice of the few idiots out there who make stupid comments, you have each other and you should be proud of the example you are setting. Having just watched your latest documentary, I'd just like to wish you and Laura all the very best in your journey to become parents. I am so much more positive now and life is good because of that,” he added. In an ideal world people like you would be the first in line to have children. Treacher Collins Syndrome Symptoms range from barely noticeable to severe and disabling, but typically include smaller or the absence of cheekbones, droopy eyes, and deformities of the ear canal causing hearing loss. For what its worth I dont think you would be disrespecting anyone by having IVF selection as you have thought about the issue so carefully and you are are putting the welfare of your future child at the centre of your decision. I wish you all the best for your future and will be sure to check in on how you are doing. tomorrow!Also I wish you the best of luck in raising money for Little Ellie, make sure to keep us updated :), Complain about this comment (Comment number 3), I think this world needs more people like you,you really are a good egg.Will be watching the next show.Best wishes to you both and carry on the amazing work.x, Complain about this comment (Comment number 4). Now 33 years old, Jono was born with Treacher Collins syndrome which is a genetic disorder that affects the facial bones development while in the mother’s womb. The 30-year-old has made it his mission to inspire others with Treacher. You can see So What If My Baby Is Born Like Me on BBC Three at 2100 BST on Tuesday 19 April 2011 and after on BBC iPlayer . The main feature at the moment is my blog where I write and comment about issue. Jono Lancaster was born with Treacher Collins Syndrome, a genetic disorder that affects the development of the bones and tissues of the face. Complain about this comment (Comment number 32), Hi Jono,I think you are sooo brave and inspiring!! If you go down the IVF route, it is a long emotional journey but so worth it, if you are lucky like Steve and I, and get the reward at the end.Best wishesShona, Complain about this comment (Comment number 94), Dear Jono, I am currently watching your newest documentary about you and your partner having a baby, and I just felt compelled to write to you and tell you how fabulous you are. I cried for you over your agony in regards to your morals but don't allow anyone to judge whatever decision you and Laura make - it is your decision alone. What is Jono Lancaster's net worth in 2020? As a teacher I think it is fantastic that you are going in to schools and talking to children raising awareness in genetic disorders and being such a positive role-model for children like Ashley and his peers. Hi!