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Our daughter was born with Pierre Robin's and Stickler's Syndrome. She has a cleft palate that affects the hard and soft palate, but not the lip. When she was nine days old she took a marked dislike to the bottle. A bout of thrush in the mouth, didn't help. She seemed scared of the bottle, of the milk spurting into her mouth and hitting the back of her throat.
Every feed ended in tears for both of us. A representative from the distributing company came to the hospital demonstrating various things including the new Haberman Feeder*. The sister in charge begged to borrow it and try feeding Belinda. From the first time it was like feeding a different baby. It was slow going. We brought her home at seven weeks by which time she was drinking 100ml an hour. The design of the bottle is perfect. My husband and I are both totally blind. With the lines on the teat and the markings on the bottle being raised, we can measure the milk and operate the bottle without any assistance. The bottle is a God send. Belinda was one of the first babies to use this bottle in Australia. We were so lucky it arrived when it did and we cannot thank you enough for inventing it. It just goes to prove that mothers really do know best!
Heather Gleeson, NSW, Australia.
My little boy James was born severely asphyxiated and they never expected him to feed orally. The Haberman Feeder* is marvellous for him and I only wish people were made aware of this wonderful invention. It will certainly recommend it to any of my friends whose children suffer with feeding difficulties or colic.
Mrs. G. Griffin, UK
These bottles are fantastic. I'm using one now on a Down's Syndrome baby with major heart problems awaiting urgent surgery. Many thanks.
Mollie Lloyd, UK
Our daughter Kimberley was born with a respiratory problem known as Pierre Robin syndrome. Despite gloomy predictions, Kimberley has gone from strength to strength and your feeders have assisted the development of the muscles surrounding her jaw…
Please accept our heartfelt thanks….
Margaret and Ray Hutt, Australia
Sophie, who is six months old and now weighs 6lb 2oz, has a condition called Patau syndrome and is not expected to live for much longer, so all we can do is love her and make life as easy and as comfortable as we can for her. We have been using the feeder for just over one week and she has put on 6oz…
To us, Sophie's Haberman Feeder* is priceless.
Sue & Sophie Havill and family
Our son was born seven weeks premature and suffered from a cleft lip and palate. Therefore, he was unable to breast feed and conventional teats were not suitable. We tried your valved teat at two weeks and he started feeding much better…He is not growing fast. Many thanks for your great idea.
It is certainly making quite a difference to our lives and has helped to make feeding the enjoyable time it should be.
Caroline & Jamie Wilson and baby William, UK
*Haberman and Haberman Feeder are registered trade marks. |
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