PLEASE CHOOSE A REGISTRY LIST TO ADD YOUR GIFTS TO: Messes are easy to wipe down since there’s no place for food to get stuck, plus a magnetic tray you can use with one hand makes things that much simpler when juggling a meal and baby all at once. INNOVATIVE: smart products that do more One handed, tray attachment, with embedded magnets. 3 different height settings. Tray adjusts to 3 different positions. Transitions from a 5-point harness to a 3-point harness as your child gets older. Tray locks into place and requires a parent to squeeze a latch to unlock it with just one hand. Easy-to-clean seat and tray. This item may be shipped via Standard, Expedited or Express shipping giggle currently only ships to locations within the 48 contiguous states. Unfortunately, we are unable to ship internationally or to PO Boxes, APO/FPO addresses, Hawaii, Alaska, or US Territories. Please change your search or select different filters!This is the five-year-old boy who stands at just 2ft 11 inches making him smaller than his toddler sister after an ultra-rare genetic condition stunted his growth.

Ryan Cahill, from Weston-super-Mare, Somerset, is the only person in the world with a combination of two medical conditions that make him so small. He has genetic disorder Bloom Syndrome, which promotes short stature, and another mystery condition that doctors have not yet been able to properly diagnose. Five-year-old Ryan Cahill, from Weston-super-Mare, Somerset, is the only person in the world with a combination of two medical conditions that make him so small. He stands at 2ft 11inches Little Ryan, who has a genetic disorder called Bloom Syndrome, is dwarfed by his younger sisters Lisa-Marie, three, and Lacey, two. Lisa-Marie can even pick him up (pictured right) It means his proud mother Corrie, 28, has to buy his school uniform from specialists in the US and he is dwarfed by his younger sisters Lisa-Marie, three, and Lacey, two. The youngster, dubbed a real-life Tom Thumb, is also so small that he can fit into boxer shorts which were bought for his Build-a-Bear teddy.

But what he lacks in stature his family say he makes up for with his big personality, because Ryan loves nothing more than making friends with strangers and giving hugs. His mother said: 'Ryan weighed four pound eleven ounces when he was born, he was smaller than a premature baby. 'We had to buy dolly clothes because premature ones were too big. 'He got his clothes wet recently and we dug out a six to nine pair of dungarees that fit perfectly, we didn't tell him they were six to nine months. It means his proud mother Corrie, 28 (pictured together), has to buy his school uniform from specialists in the US and he is dwarfed by his younger sisters Lisa-Marie, three, and Lacey, two Ryan, five, is pictured with his 11-year-old step-sister Jade (left) and step-father Barry Cahill Ryan (second from left) is a similar height to his two sisters, who are both younger than him 'We pay £56 for school trousers from America and have to roll up and stitch his jumpers, every bit of clothing has to be altered.

'When he first started potty training we bought him Build-a-bear teddy boxers which he still wears today. 'If he's got a point to prove he will prove it, his whole personality is bigger than him, it shines through.table chair rental louisville ky 'Like most children he can have a bad attitude, he'll stomp upstairs, slam the door and scream the house down.'lazy boy chair measurements Ms Cahill was told she'd never have children again following the tragic death of her twins Phoebe and Jaden in 2007. jumbo bean bag chairs canadaPhoebe was stillborn and Jaden passed of cot death aged 12 weeks.cheap game chairs xbox 360

She fell pregnant with Ryan a short time later but when doctors spotted that he had stopped growing in the womb at 20 weeks, she was advised to have an abortion.stair chair lift around corners However, she said: 'I told them I wasn't getting rid of my miracle baby.'wedding chairs for sale in ontario Ryan was just four pound eleven ounces when he was born - smaller than a premature baby Ryan's step-sister Jade, 11, (pictured in a photo of them when they were younger) is hands on Bloom syndrome is an inherited disorder characterised by short stature, a skin rash that develops after exposure to the sun, and a greatly increased risk of cancer. People with Bloom syndrome are usually smaller than 97 per cent of the population in both height and weight from birth, and they rarely exceed five feet tall in adulthood.

Affected individuals have skin that is sensitive to sun exposure, and they usually develop a butterfly-shaped patch of reddened skin across the nose and cheeks. A skin rash can also appear on other areas that are typically exposed to the sun, such as the back of the hands and the forearms. Small clusters of enlarged blood vessels (telangiectases) often appear in the rash. Other skin features include patches of skin that are lighter or darker than the surrounding areas. People with Bloom syndrome have an increased risk of cancer. They can develop any type of cancer, but the cancers arise earlier in life than they do in the general population, and affected individuals often develop more than one type of cancer. Individuals with Bloom syndrome have a high-pitched voice and distinctive facial features including a long, narrow face; a small lower jaw; and prominent nose and ears. Other features can include learning disabilities, an increased risk of diabetes, chronic obstructive pulmonary disease (COPD), and mild immune system abnormalities leading to recurrent infections of the upper respiratory tract, ears, and lungs during infancy.

Men with Bloom syndrome usually do not produce sperm and as a result are unable to father children (infertile). Women with the disorder generally have reduced fertility and experience menopause at an earlier age than usual. Doctors were left baffled by Ryan's condition until last June when he was diagnosed with Bloom syndrome and another mystery condition they haven't yet been able to pinpoint. Bloom's syndrome is an inherited disorder that causes short stature, a rash that develops after expose to the sun, infertility in males and an increased risk of cancer. Ryan also doesn't produce a growth hormone so needs to have injections given to him by his step-father Barry, who he calls 'daddy'. He also has to wear glasses, struggles with his hearing, he can't be in direct sunlight and has to wear sunglasses, hats and full factor suncream all year round. His small stature means he can be picked up by little sisters - much to his frustration - as well as step-sister Jade, 11.

His mother said: 'Ryan gets upset because all his sisters can pick him up, Lacey can lift him up and throw him over her shoulder. 'He has trouble reaching things and he can't play for as long as the girls because he gets tired. 'I never knew children grew so quick until I had my daughters, it's exciting to watch two different sides of it. 'Jade loves him to bits and the younger girls are best friends with Ryan.' But the bubbly boy loves nothing more than working in his step-father's shop - where he wears a specially made uniform. 'He greets and serves every customer and always persuades them to buy something,' said Ms Cahill. 'He is very cuddly and will have a hug with everybody.' The clever youngster is in his second year at Walliscote Primary School in Weston-super-Mare, where teachers have made sure he has all he needs to keep up with his mates. He has a higher chair to reach his desk, and uses a special buggy for school trips to save his legs.

Lisa-Marie, three, with her five-year-old brother Ryan at their home in Weston-Super-Mare The youngster, dubbed a real-life Tom Thumb, is also so small that he can fit into boxer shorts which were bought for his Build-a-Bear teddy. Despite his height, he still joins in activities According to his family, many people with Bloom syndrome don't live into their thirties due to an increased risk of developing cancer. But Ms Cahill, who also lost a two-week-old son due to a large obstruction in his kidney, is determined to be brave for the youngster. She said: 'He has a lot of questions and I don't have the answers. The main question Ryan asks is 'am I going to die Mummy?' 'What do you turn around and say to a five-year-old? 'Losing Ryan will be like losing the world. I don't know how the girls will cope. 'I have to be brave, inside I'm screaming. Doctors were left baffled by Ryan's condition until last June when he was diagnosed with Bloom syndrome and another mystery condition they haven't yet been able to pinpoint