** Doctors see something coming out of baby’s head, when they find out what it was, it left them in Awe

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I see something coming out of baby’s head when they find out what it was it left them in awe giving birth to a baby is not an easy job having said that it is the most happiest moment a woman can experience that feeling cannot be experienced in words once the process gets over and you see the baby face for the first time you’ll be cherishing it for a lifetime if possible take pictures of the first

 Glimpse of you and baby bonding and attachment happen when you consistently respond to newborns with love warmth and care newborns use body language to show when they want to connect with you good ways to bond with newborns including smiling eye contact singing reading and cuddling most women would say they enjoy childbirth there are parts of pregnancy that are definitely enjoyable like

 Feeling your baby move for the first time and things like that but most of it is not physically enjoyable for most women yet most women would not trade the experience of pregnancy and childbirth for the world it’s like someone who runs a marathon or does something extremely hard and taxing it’s something you prepare for but not necessarily enjoy while it’s happening the perk is that you can look back on it and see how much it made you grow

 Emotionally and how much confidence it gave you for your tolerance and strength a change in the baby’s genes such as a mutation or extra chromosomes some types of medicines taken during pregnancy used during pregnancy a birth defect also called a congenital disorder or congenital anomaly is a health problem that a baby is born with there are many different types of birth defects and they can range from mild to severe

 The story of noah wall is truly amazing as it’s a case of brain growth from an anatomical point of view without a doubt this story represents scientific curiosity but it goes beyond that it also broadens the knowledge regarding the human brain in short this amazing case of brain growth is related to an english boy named noah wall he was born with only two percent of his brain the fact that he was able to live is an unusual fact

 In itself however the most incredible thing of all is that over the years and thanks to care and treatments he managed to develop up to eighty percent of normal brain volume now it’s impossible to overlook something regarding this already fantastic case of brain growth we’re referring to the fight that noah’s parents had to carry out his mother and father are the reason that this british

 Boy is alive undoubtedly this story is an example that some limits only exist in the mind this is a case of foolproof faith effort and perseverance noah wall from carlisle cumbria developed a rare brain condition in the womb and his parents michelle 49 and rob 55 were told by doctors he would likely never walk talk or eat on his own instead however noah has seen his brain grow from two percent up to eighty

 Percent he’s been able to surf and ski and now dreams of one day becoming an astronaut noah was diagnosed with spina bifida which is when a baby’s spine does not develop properly early in his mom’s pregnancy with doctors revealing he would be paralyzed from the chest down early scans also showed he would likely be missing a quarter of his brain at birth due to a parensaphalic cyst on his head which was destroying his brain

 Noah also had a rare condition called hydrocephalus which is a life-threatening condition that leads to an accumulation of fluid within the brain as the pregnancy progressed noah began to develop more complications and doctors believed he could develop edward syndrome and pataus syndrome a baby with edward syndrome has three copies of chromosome number 18 instead of two just 13 and 100 babies born alive

 With edward syndrome live past one pataus syndrome is a serious rare genetic disorder caused by having an additional copy of chromosome 13 only one in 10 children with this disorder survived past a year a do not resuscitate order was placed on noah and his parents were asked five times if they wanted to terminate the pregnancy noah’s mom michelle recalls how difficult her pregnancy was and she

 Didn’t know whether her baby would survive until the moment he was born the distraught parents had gone through the heartbreaking process of choosing a coffin and were arranging for a funeral before noah was born as a parent you don’t want to believe what they’re saying but it’s reality michelle explains but you’ve got to go home and tell your family that we might have to bury him we always tried to be positive always even though we were

 Given such a horrendous situation but against all odds noah was born on march 6 2012 weighing nine pounds seven ounces and was able to breathe on his own his mom cried when he took his first breath as this indicated he had a chance of surviving describing the day noah was born mrs wall added the day he was born was amazing we waited with baited breath the couple were admitted to the hospital

 A week before mrs wall’s due date because the pressure on noah’s brain was becoming dangerous there were 12 doctors in the operating theater as experts performed a c-section but as he came into the world they were given a sign mr wall said he let out this amazing scream we knew there was power there now the families send regular updates to doctors who told them noah wouldn’t make it

 Mrs wall said he’s extraordinary we send them emails and pictures and we take them presents at christmas time the couple have been given an assessment at a pioneering australian clinic where medics combine physiotherapy and cognitive training to train the brain he’s confined to a wheelchair but with the help of the clinic hopes to try out for some of his favorite sports noah took one life-affirming scream when he was born and tears just rolled down

 My cheeks michelle explains it was incredible it was emotional shortly after his birth an mri scan revealed noah was actually born with just two percent of his physical brain after seven weeks he had a shunt put in his head and a soft tube to drain the liquid down his neck into the abdomen he’ll likely require tests and surgeries throughout his life michelle who works as a full-time carer said doctors told us he would be in a

 Vegetative state he wouldn’t be able to communicate they told us he might not be able to speak hear eat or anything but he can tell the time he reads he does math he loves science he can talk about the solar system he has incredible dreams and even more incredible knowledge earlier this month noah celebrated his ninth birthday i love having people around on my

 Birthday this birthday was different but it was still special noah says with a special day michelle said noah’s birthday celebrations are emotional for the family every year as it reminds them of how far they’ve come and how extraordinary noah’s progress has been noah who uses a wheelchair has revealed he hopes to play football one day when i went to newcastle stadium i was on the grass and i was amazed one day

 I’m going to run and score a goal he says he has also outlined his hope of one day falling in love and having his own children although noah has already had 11 surgeries and faces a lifetime of operations the family says they’re still determined and hopeful he will get to fulfill his dreams it’s been an absolute joy to see him grow up and see him become the unique boy that he is michelle explains it’s

 Astonishing to me how smart he is we’ve spent a lot of time with him and every single day he does something that impresses me i’m so extremely proud of him he’s my son his goal in life is to run it’s what he wants to do i’ll help him all i can and always be there for him noah is a proud patron of variety a charity which works with disabled sick and disadvantaged children as well as the music man project which puts

 Disabled children on the uk’s biggest stages as the pregnancy progressed noah began to develop more complications and doctors believed he may develop edward syndrome and patau syndrome a baby with edward syndrome has three copies of chromosome number 18 instead of two and sadly just 13 and 100 babies born alive with edward syndrome live past one patau syndrome is a serious rare genetic disorder caused by having

 An additional copy of chromosome 13 and only 1 in 10 children with the disorder survive past a year but thankfully against all odds noah was born healthy and was able to breathe on his own she added noah took one life-affirming scream when he was born and tears just rolled down my cheeks it was incredible it was emotional after seven weeks he had a shunt put into his head and a soft tube to drain

 The liquid down his neck and into his abdomen which will likely require tests and surgeries throughout his life the alert child has many interests and ambitions even though he faces a number of surgeries his mother told the media but he can tell the time he reads he does math he loves science he can talk about the solar system he has incredible dreams and even more incredible knowledge it’s been an absolute joy to see him grow up and to see him become

 The unique boy that he is michelle explains it’s astonishing to me how smart he is we’ve spent a lot of time with him and every single day he does something to impress me as part of the music man project a music education service for children and adults with a learning disability noah took part in a concert at royal albert hall it’s unclear from media accounts whether noah’s brain was absent or simply very

 Compressed estimated to be about two percent at birth it was about eighty percent of normal on examination when he was three years old what is and isn’t necessary for the human brain to function can sometimes seem to be far from exact science at present it’s sobering to think that many noahs may have been deemed incapable of an assisted normal life and allowed or assisted to die what is hydrocephalus hydrocephalus is a

 Buildup of fluid on the brain the excess fluid can put pressure on the brain and which can damage it noah developed congenital hydrocephalus present at birth caused by the spina bifida he was also diagnosed with long-term complications can include learning disabilities impaired speech memory problems short attention span problems with organizational skills vision problems such as squint and visual impairment and problems with

 Physical coordination the condition can usually be treated using a shunt a thin tube that is surgically implanted in the brain and drains the way the excess fluid let yourself enjoy your baby the same way any new parent would by cuddling and playing watching for developmental milestones even if they’re different from those in other children and sharing your joy with family members and friends some parents wonder if they should send

 Birth announcements this is a personal decision the fact that your baby has a health problem doesn’t mean you shouldn’t be excited about the new addition to your family understanding your child’s condition can help you get them the best care possible go to your child’s doctors and care team with any questions.