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 . Bye for now -look after yourself and also your darling LauraSee you soon and all love Betan (and Tiggie) xxxxxxx Tomorrow I will try to send you a photo of Tiggie -he is completely an indoor cat -not wise these days to let any cats out -even the RSPCA advise any cat owners to keep their cats indoors -Byeeeeeeeeeeee x x x x x x, Complain about this comment (Comment number 67), What a great documentary ! Good luck mate. Complain about this comment (Comment number 10), What a great bloke you are Jono. and whati wanna say to u is tht u r an inspriation to the world xx, Complain about this comment (Comment number 63), Just watched the programme, so what if my baby is born like me, found it very moving, you both are so brave and I wish you both every success in the future, Complain about this comment (Comment number 64). I honestly wish you and Laura all the best for your future together!! 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. Complain about this comment (Comment number 28). All I really wanted to say though is that I wish you both the very best of luck whatever your final decision. Thank you so much Jono for sharing your journey with us. I wish you and your family only the very best for your future and I do hope to see a photo of you holding your own perfect baby (because that's what it will be whatever path you both decide to take) very soon.With love and admiration ....Sue, Complain about this comment (Comment number 85), Jono, your programs have reduced me to tears every time (though i cried at neighbors the other day) and i really admire you.I just wanted to say to Laura that i've been through IVF myself and my reaction to the idea of the egg collection procedure was much the same as yours, but when the time came they gave me a sedative (not a general anaestetic) which worked wonders, i didn't feel a thing, and now can't remember any of it!I really hope things work out for you two in the future and that whatever you decide you enjoy it.

I'd like to wish you both the very best in all that you do and long may it continue (what you're doing!!).

I think all the negative comments on the site Jono mentioned are the disabled people in this world and they don't deserve any love. 05/17/2020; Author ad. She is a very lucky priviledged girl to have you by her side and how I really wish that eventually your dreams and hopes of having a darling baby materialise -you would both, I feel sure, make wonderful loving parents whether your baby is completely healthy or not. You are a beautiful person, with a beautiful girlfriend and beauty is not a condition. Keep your heads high guys, the treacher collins isn't who you are Jono, and shame on the idiots, hard hearted enough to even think, much less write things about you both!

Complain about this comment (Comment number 60). Learn more about our, iy_2020; im_11; id_02; ih_23; imh_26; i_epoch:1604388386215, py_2020; pm_11; pd_02; ph_14; pmh_12; p_epoch:1604355140631, link-block-publisher; link-block-publisher_link-block-publisher; bodystr, pn_tstr:Mon Nov 02 14:12:20 PST 2020; pn_epoch:1604355140631, https://www.littlethings.com/jono-lancaster-abandon-baby/. At the age of 26, Jono is happy with how he looks, but the genetic disorder that affected the way his facial bones developed in the womb has caused him years of anguish. 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. Copyright © 2020 BBC. Ultimately, as your mother said, wrt IVF, you are thinking of your child rather than your own morall maze. Complain about this comment (Comment number 81), Hi Jono and Laura, I watched both of your programs. Well done Jono and Laura for raising awareness can't wait for the next documentary :), Complain about this comment (Comment number 68), Hi Jono I've really enjoyed watching your documentaries so far, I hope you do continue with your baby plans!! I have a genetic condition myself called osteogenesis imperfecta, and like you I have a 50/50 chance of passing it on. Jono Lancaster was born with Treacher Collins Syndrome, a genetic disorder that affects the development of the bones and tissues of the face.

I wish you all the best for your future and will be sure to check in on how you are doing.

I hope you & Laura will continue to have a happy life & that someday you make your "mum" a very proud grandma! Your sensitivity to others is amazing. Jono Lancaster, a 33-year-old man from England, was born with Treacher Collins Syndrome that caused deformities on his facial structure. You are awesome! Even when he tried to contact his birth parents as an adult, he was met once again with rejection. What ever decision you and your girlfriend come to, it will be the right one as everyone can see you'll support that baby wether its adopted or not, genetic disorder or not. It must help a great deal having someone offer understanding AND practical advice. I just want to say that I have watched both your documentaries now and that I am truly amazed by your courage and determination in raising awareness of Treachers Syndrome. In this article, we take a look at Jono Lancaster's net worth in 2020, total earnings, salary, and biography, Jono Lancaster. hope you have a lot of luck with your child. Complain about this comment (Comment number 15).

Just have to say how brilliant I think you are for doing what you're doing. You are a fantastic role model though Jono and should be a full time councillor and motivator for kids with similar problems to you, you relate so well to them.

Just saw you again on BBC 3. Finally, I want to wish you the very best of luck whatever you decide, i'll be watching any future programmes you do. At least people with genetic conditions have the option to decide which route to take. God bless and good luck. Complain about this comment (Comment number 71), I have watched So What If My Baby Is Born Like Me? I will be sat watching 'So What If My Baby is Born Like Me?' Jono came to speak to us as part of our anti-bullying week. “I don’t want the children growing up with Treacher Collins now to make the same mistakes I did,” Jono said. YOU ARE A TRULY BEAUTIFUL PERSON JONO - AND YOU AND LAURA MAKE A TRULY BEAUTIFUL COUPLE. My heart goes out to you both with the decisions you're facing re a baby, I hope things work out for you x, Complain about this comment (Comment number 7), i think you and your girlfreind are amazing ..i think that it would be a lot easier for people if children were learnt about it while they are in primary ..i have epilepsy and i know its not the same i found out i had it when i was ten because i had a seizure in infront of the class and because non of the teachers explained about it i got teased intill i was in yr nine and i took it upon my self to do an assembly to explain what i had and all the children understood i think if alot of school did this children wouldent be scared to ask about it and wouldnt grow up to be so niave i think that you two are amazing and that you should keep on going strong the way you are because you are giving alot of children hope, Complain about this comment (Comment number 8), Just watching the programme on bbc3 and just want to say i think you are a lovely looking guy and it is totally obvious what laura sees in you! Good luck!!

dokumentarni, Jono Lancaster is a English Person from England, United Kingdom. The Heart Of A Champion: Boy Born With No Legs Pursues Baseball Dreams.

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