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. The nasty, ignorant comments you received from some pathetic idiots are not even worth reading.

I don't think it really matters what a person looks like -its what they are and who they are -and you Jono are a beautiful loving caring person, and its obvious that Laura thinks the same.Its so easy to see past your face and to easily find the wonderful person inside. A baby born with facial deformation was abandoned by his parents at birth, but he is now inspiring millions of people! A real credit to young people who are constantly derided by the media. When there is good people like you in the world, the world is a better place to live. Complain about this comment (Comment number 44), Hi Jono & Laura...You're a truly inspirational couple, just finished watching the program and wanted to send you all the luck in the world as you start your family. While the wall-to-wall mirrors were a form of torture, the rest of the job was a blessing. Free Speech - Higher Education - Is it worth it? If you aren't sure what RSS is you'll find our beginner's guide to RSS useful. He aims to inspire those who share his condition, so that they may also live a normal life.

Ultimately, as your mother said, wrt IVF, you are thinking of your child rather than your own morall maze. Laura is right Jono, you have the option of having a baby without the syndrome, without passing on any pain or suffering, thats a great option to have and not morrally critical of others who have the diagnosis. This is a condition that is hereditary meaning that it is passed down thru family generations.. A Man From Yorkshire Flew To Australia To Meet A Child, Jono Lancaster is Inspiring Millions Despite Parental, New dad with severe facial disfigurement defends decision, Jono lancaster, amtrak train station lancaster, pa has an.

Complain about this comment (Comment number 32), Hi Jono,I think you are sooo brave and inspiring!! But since then, Jono has become an inspiration to people with the same condition, and their families, by telling his story. I watched the first documentary as well and it is so fantastic to see your lovely personality shining through. I would just like to send my best wishes to you both for the future, and i hope you get all you desire and deserve in the near future. “My birth parents still don’t want anything to do with me. Both my son and myself will continue to follow your journey and support you and Laura every step of the way. I wish you and your lovely partner all the vest best that life has to offer you. Good Luck, Complain about this comment (Comment number 17). I think your (both of you) analysis of the moral dilemas are spot on and to be congratulated.

Good luck to you and Laura with whatever the future holds.Em, Complain about this comment (Comment number 43). I have had lots of nice comments on my blog about you. Please contact us at Rights@LittleThings.com. It also turned out, he did NOT have the disorder, but completely a different one, that was undetected until birth, well as far as I knew, but I think I was kept in the dark. Just keep doing what your doing. Parents See Baby’s Face Is Disfigured, Then Abandon Him 36 Hours After He’s Born. I can see the dilemma you're facing but feel you're doing so with remarkable maturity and sensitivity, parenthood is always a big step and I think it's a shame more people don't understand this beforehand! The BBC is not responsible for the content of external sites. Thankfully, due to his work and newfound status as an inspiration to these children, he was able to connect with one family in particular, and quickly became part of it.

Hi Jono, I was really touched by your programme. Jono Lancaster, a 33-year-old man from England, was born with Treacher Collins Syndrome that caused deformities on his facial structure. Performance & security by Cloudflare, Please complete the security check to access. While you will be able to view the content of this page in your current browser, you will not be able to get the full visual experience. Your decision on the way forward is a personal one, that only the pair of you can make and whatever it is it, will be right for you.Ignore your critics,ignore the shallow bullies, revel in being you and embracing all that makes you different. i aslo think my two older boys have the same genetic condition as me brandon went through numerous operations when he was younger and my little boy cant walk talk or eat and hes not yet two was hoping the genetics test would find out why he cant do anything so not only do we have a condition called nail patella syndrome our poor little man may have another underlying condition also :(i took alot of stick from teachers and bullied at school because my bone structure was different to everyone elses but im a tough person i dealt with it my own way - the hardest bit was the teachers picking on me because i couldnt do certain things or id hold a pen and get through things in different ways you learn to adapt.would it have changed anything if id have known about my condition earlier on in life about the decision to have children im not sure but they are here now and im as good a parent as anyone else.

Completing the CAPTCHA proves you are a human and gives you temporary access to the web property. I hope the people who say they shouldn't be together don't find love and happiness.
If I were you I wouldn’t pay any attention to the nasty people and I certainly wouldn’t look up their websites. Complain about this comment (Comment number 77), i was so moved by your personal journey, that it compelled me to contact you, i thought what a couragious, well balanced and wonderful young man you are, and the sheer determination you show to get on with your life is truly remarkable. Complain about this comment (Comment number 40), You two are great! I just wanted to say how brave you both are. I hope that you have your baby/babies and respect your decision totally. Upon seeing their son with deformities, Jono’s parents gave him up for adoption 36 hours after he was born.

The genetic engineering makes sense, because at least if you go down that path, then the guilt will feel less I would have thought. In an interview with Adelaide Now, Jono says: 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. I can only wish you all the best for the future and whatever decision you come to.......not an easy one for either of you. I don't know what I can do, but I'll do something to raise awareness like you. Keep doing what you are doing and dont take any notice of narrow minded critics You are both beautiful xx, Complain about this comment (Comment number 72), Hi Jono and Laura. I had a child that was a one in `100,000 chance, no genetic links at all, but the effects were the same, the guilt is enormous, even when there was nothing you could have done to stop it. Its sad that there are shallow deluded people who think that because they have regular features they are somehow superior and have the right to be offensive. I'd like to wish you both the very best in all that you do and long may it continue (what you're doing!!). You and Laura are a truly inspirational couple. You're going to make brilliant parents. As such I think you will be excellent parents -far more than some people that don't care about theirs. hope you have a lot of luck with your child. Complain about this comment (Comment number 18). 18 November 2010 Like many 26-year-olds, Jono Lancaster has a job he loves, a beautiful girlfriend and takes pride in his appearance. God bless and good luck. Complain about this comment (Comment number 57). And then not long ago I spotted my parents and sister watching it as well.

Good luck to you both and the other wonderful people also shown on the show - you are all inspirational and I wish you strength and happiness.

These physical differences are what caused Lancaster’s birth parents to abandon him 36 hours after he was born. ... Jono Lancaster has no cheekbones or … I saw the first programme and thought you were brilliant, especially with the kids at school .
I look forward to seeing you both living the same experience you deserve it......take care and good luck with everything..ps I love your mum she is a truly wonderful lady the type u want to cuddle xxxxxx, Complain about this comment (Comment number 48), I have just watched your programme and just want to say you and Laura are amazing . You may need to download version 2.0 now from the Chrome Web Store. 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. Complain about this comment (Comment number 21). Going to make a drink now -our darling Tiggie (cat) is fast asleep on his chair but just ONE magic word would wake him up immediately PRAWNS !!!!! I wish you both all the very best for the future. 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. Complain about this comment (Comment number 28). Jono and Laura want a baby but there is a 50% chance Jono's rare genetic condition will be passed on to their child.

Jono Lancaster Follow Up: So What If My Baby Is Born Like .

They have a lot to learn about what's important in life! :), Complain about this comment (Comment number 97), Hi JonoI just wanted to drop you a line to let yourself and Laura know that you are both an inspiration to so many different people out there. A truly remakable story. Complain about this comment (Comment number 61).

Having a child is not a simple decision for anyone. Any child or children that you have will be one of the luckest children around. Jono Lancaster was born with Treacher Collins Syndrome, a genetic disorder that affects the development of the bones and tissues of the face. Please consider upgrading your browser software or enabling style sheets (CSS) if you are able to do so.

Complain about this comment (Comment number 13). He explained about Treacher Collins Syndrome and some of the experiences he had whilst growing up with the condition.

You are a truly remarkable person! Jono Lancaster / Facebook. I know from personal experience it is only you that can make the decision and that decision is the right one for you two. If you are on a personal connection, like at home, you can run an anti-virus scan on your device to make sure it is not infected with malware. I was offered a termination - I didn't ask for it! •

Keep being yourself buddy and I'm sure you will have a very happy future =D, Complain about this comment (Comment number 11), Hi I have seen a few programs with you and your partner, you come across as an articulate and happy couple, I wish you well with all your endeavours.I understand social networking sites can be good, but some people are jealous and narrow minded.All the best to both of you, Complain about this comment (Comment number 12). 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).


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