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I wish we had as many TV shows like 'Little Big World' as they do in the US. Ellie Simmonds & Jennette Tough of The Krankies .are the only UK celebrities I know. Which is a shame, there should be way more. I'm a brand new subscriber watching from southern England.👍

you are beautiful

I'm a 4'8 adult but I've never been diagnosed with anything. I have regular sized limbs so I guess I'm just short then

cant lie still looking sexy

Hello im from Philippines i have 2months old son I don't know what kind of dwarfism he have.

I watched a lot of videos about people of small stature. I knew well about the disease achondroplasia, but never heard about my own disease hypochondroplasia. As I understand it, hypochondroplasia is much less common and there are very few videos on the Internet with such people. We are rare

I can keep listening to you forever. Not just when you talk about your height but also your philosophy in general. It is painful to see that you have to experience pain but I wish from the bottom of my heart that you always find strength when you need it. ❤️❤️❤️. Personally speaking, it is absolutely impossible to not fall in love with you.

I feel fortunate that I found your channel. People who bully and are unkind are dead inside. Please do not be bothered by them.

I congratulate you for overcoming all your struggles and sticking with LIFE when it was hard to live. As a fellow human, I absolutely admire your courage. May we find ways to reduce the suffering in future.

I'm 68 and hypo. Life's been hard but I worked my behind off and have retired successfully. No one realizes the pain of being called a munchkin, shorty, and tons worse while I was working hard in my career, than you and I do, and many more like us. Meanwhile enduring the physical pain our bones give us that we silently endure. Thanks for being so brave in speaking up. Sending you hugs and love and I'm here if you want to talk more. Jan

Hi Amy, I came across your profile / videos looking for more information on a person with Hypo and how they get on with things in the real world. As I’ve just found out in the third trimester of my pregnancy that my baby is also Hypo. I don’t know how I am going to cope with people calling her a ‘midget’. I feel like I will get so angry with them. I want to be really strong for her and show her that yes there will be struggles but there is going to be so much love and fun in life too. I’m hopeful that the world is becoming more diverse. But I do agree with you that bullying will continue to be around and I just need to find a way to build her up give her the confidence to say “so what?” Listening to you talk about it is a good insight and I appreciate you speaking out. I’m from London uk 🇬🇧

Thank you for sharing this. My 22 year old son was diagnosed with hypo when he was a year old. He’s 4’9 and an active Sailor in the US Navy. He’s struggled so much, I think it’s even harder for him because of the profession he’s in…male driven. He’s attempted suicide a couple of time and thank the Lord he’s still here. I wish he’d look into the LPA for support but he never has. I admire you so much for sharing your story 💛

Hello I love your accent it sounds Irish or Scottish.

Good keep it up 🙂👍

Hi Amy I have hypochondroplasia a slightly milder form. I was born in 1960 when medical knowledge was limited in South Africa. It was also the apartheid area with segregation of the races. My parents noticed I had a problem after I turned 1 and began to walk. I was blessed to be taken to a Dr Sweden in Queensburgh Durban. He checked me every Sunday and I was always excited to see the Dr. I was treated to a lolly pop every week. In that time he educated my parents and he told them to treat me as normal as possible. At about 3years I was given a brace that I had to sleep through the night strapped unable to move. At about 4/5 I was given metal stuff strapped to my legs with a boot. This was very heavy and uncomfortable. I was treated as a normal child and fortunately grew up well adjusted and was confident. I completed my studies, went to university and then went out to look for a job. I was very lucky to work for a large chain store and then a multinational company. I have 2 children. 1 was normal the other inherited my condition and I did lots of research and she was operated when she was 2 1/2 years. Today she is also blessed to be working for a multinational company. Before I retired I won a competition and competed against colleagues and came 2nd in South Africa. The prize was a trip to the French/Italian Riviera for 2. I am sharing this with you to let you and others like you and me to know, we can achieve anything we set our mind to. We may have limitations with our height but it does not stop us achieving our dreams, being the best version of ourselves, being confident and set goals and aspirations like any other person. I think sometimes with this condition we become over achievers. I would like you to be the best version of yourself, enjoy your life and most of all have fun. I am a grandmother, with 2 professional children 1 is a Environmental research scientist and the other is a Graphic designer. I pray all your dreams aspirations come true. We have no control of genetics but we can have control of our life. God Bless you

You have a beautiful face ..stay strong ..we all are finding purpose in this temporary life..you are a pure soul

I’m not sure how I ended up here, but I’m glad I clicked on your video. You’re a very strong and brave woman. I’m so sorry for the nastiness you’ve had to endure from others, but good on you for taking your power back. Thank you for sharing your story ❤️

Thank you for sharing your experience. 💕💕 I’m so thankful I came across your video today. My daughter was just recently diagnosed with a FGFR3 mutation at 15 years old. I’m just trying to understand what she’s going through and your early experience sounds exactly like her.