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Tag: Brain

  • URMYWO Baby Toys 0-6 Months, Black and White Sensory Toys Brain Development, Tummy Time Toys, Soft Baby Book, Baby Essentials for Newborn 0-6-12 Months Newborn Toys Baby Gifts

    URMYWO Baby Toys 0-6 Months, Black and White Sensory Toys Brain Development, Tummy Time Toys, Soft Baby Book, Baby Essentials for Newborn 0-6-12 Months Newborn Toys Baby Gifts


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    From the brand

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    URMYWO Baby Toy

    We focus on researching and developing baby toys, high quality baby toys, for 0-12+months.

    Baby Sensory Toy

    Newborn Essentials

    Baby Product

    Sensory Toys for babies : Baby born with blurred vision, and gradually increased on 3 months. This high contrast baby book helps stimulate development in the retina and the optic nerve, to train step by step and activate the brain. This sensory book contains 11 different patterns which basically are black and white patterns and 1 baby-safe mirror, all of which will aid visual development in the early stages. Flip little red flag makes more fun for baby.
    Newborn Toys: Baby babies love these newborn toys. There is crinkle paper hiding in the page, which encourage baby to explore and gives baby endless hours of fun. The bright colors and contrast background will attract baby’s attention. Black and white patterns also help babies to develop their ability to focus their attention and concentration.
    Safe Materials&Verlcro Straps for Attachment: Our newborn sensory books from soft polyester. Non-toxic, strong stitching, hand washable, and absolutely safe for your baby. Also, there are verlcro straps that easy for keeping on a crib, stroller, baby fence or the wall.
    Ideal Toy for Tummy Time: You can also put these baby books on the floor for the tummy time. The high contrast patterns and the baby mirror can attract the baby’s attention for a long time, which could improve their fine motor skills, prevent flat head and help strengthen baby’s leg and arm muscles. Babies will enjoying touching and flipping thses sensory books, making tummy time fun.
    Great Gifts for Babies: The baby sensory toys books are lifelong and never-get-old gifts for infants and toddlers. Whatever age and gender you are planning to gift, our soft baby books are ideal newborn developmental toys for 0 – 12 month infants, perfect gift for Shower, birthdays and Christmas.

    Customers say

    Customers find the product engaging for babies, with a good design and sturdy construction. They appreciate the bold colors that are accessible for newborn vision. Many consider it a worthwhile purchase and appreciate the stimulation, weight, and size of the product.

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  • Bananas Some Very Interesting Facts and Uses

    ” BANANAS…”

    A very interesting FACTS

    Never, put your banana in the refrigerator!!!…

    This is interesting. After reading this, you’ll never look at a banana in the same way again.

    Bananas contain three natural sugars – sucrose, fructose and glucose combined with fiber. A banana gives an instant, sustained and substantial boost of energy.

    Research has proven that just two bananas provide enough energy for a strenuous 90-minute workout. No wonder the banana is the number one fruit with the world’s leading athletes.

    But energy isn’t the only way a banana can help us keep fit. It can also help overcome or prevent a substantial number of illnesses and conditions, making it a must to add to our daily diet.

    DEPRESSION:

    According to a recent survey undertaken by MIND amongst people suffering from depression, many felt much better after eating a banana. This is because bananas contain tryptophan, a type of protein that the body converts into serotonin, known to make you relax, improve your mood and generally make you feel happier.

    PMS:

    Forget the pills – eat a banana. The vitamin B6 it contains regulates blood glucose levels, which can affect your mood.

    ANEMIA:

    High in iron, bananas can stimulate the production of hemoglobin in the blood and so helps in cases of anemia.

    BLOOD PRESSURE:

    This unique tropical fruit is extremely high in potassium yet low in salt, making it perfect to beat blood pressure So much so, the US Food and Drug Administration has just allowed the banana industry to make official claims for the fruit’s ability to reduce the risk of blood pressure and stroke.

    BRAIN POWER:

    200 students at a Twickenham (Middlesex) school ( England ) were helped through their exams this year by eating bananas at breakfast, break, and lunch in a bid to boost their brain power. Research has shown that the potassium-packed fruit can assist learning by making pupils more alert.

    CONSTIPATION:

    High in fiber, including bananas in the diet can help restore normal bowel action, helping to overcome the problem without resorting to laxatives.

    HANGOVERS:

    One of the quickest ways of curing a hangover is to make a banana milkshake, sweetened with honey. The banana calms the stomach and, with the help of the honey, builds up depleted blood sugar levels, while the milk soothes and re-hydrates your system.

    HEARTBURN:

    Bananas have a natural antacid effect in the body, so if you suffer from heartburn, try eating a banana for soothing relief.

    MORNING SICKNESS:

    Snacking on bananas between meals helps to keep blood sugar levels up and avoid morning sickness.

    MOSQUITO BITES:

    Before reaching for the insect bite cream, try rubbing the affected area with the inside of a banana skin. Many people find it amazingly successful at reducing swelling and irritation.

    NERVES:

    Bananas are high in B vitamins that help calm the nervous system..

    Overweight and at work? Studies at the Institute of Psychology in Austria found pressure at work leads to gorging on comfort food like chocolate and chips. Looking at 5,000 hospital patients, researchers found the most obese were more likely to be in high-pressure jobs. The report concluded that, to avoid panic-induced food cravings, we need to control our blood sugar levels by snacking on high carbohydrate foods every two hours to keep levels steady.

    ULCERS:

    The banana is used as the dietary food against intestinal disorders because of its soft texture and smoothness. It is the only raw fruit that can be eaten without distress in over-chronicler cases. It also neutralizes over-acidity and reduces irritation by coating the lining of the stomach.

    TEMPERATURE CONTROL:

    Many other cultures see bananas as a ‘cooling’ fruit that can lower both the physical and emotional temperature of expectant mothers. In Thailand , for example, pregnant women eat bananas to ensure their baby is born with a cool temperature.

    So, a banana really is a natural remedy for many ills. When you compare it to an apple, it has FOUR TIMES the protein, TWICE the carbohydrate, THREE TIMES the phosphorus, five times the vitamin A and iron, and twice the other vitamins and minerals.. It is also rich in potassium and is one of the best value foods around So maybe its time to change that well-known phrase so that we say, ‘A BANANA a day keeps the doctor away!’

    PASS IT ON TO YOUR FRIENDS…

    PS: Bananas must be the reason monkeys are so happy all the time! I will add one here; want a quick shine on our shoes?? Take the INSIDE of the banana skin, and rub directly on the shoe…polish with dry cloth. Amazing fruit !!!

  • This Mama Knew Something Wasn’t Right

    Where do I begin? Our baby, Sienna-Rose has always been so unsteady with her balance.. we thought nothing of it at first. We assumed it was down to being short sighted and having a double squint! She was still hitting all of her milestones on time. Nothing to worry about right?

    Wrong.. fast forward to January the 30th 2019. Sienna has her injection and we were pre warned there would be a fever. She had the fever.. followed by sickness, unsteadyness, lethargy and a high temperature. We firstly rang our GP who recommended calpol and lots of rest. The sickness still came. After a few weeks of constant sickness and crying we took things further. We took her to A&E who did their checks and diagnosed “gastritis” she was prescribed a course of amoxicillin which she did dont take down neither did it fix the sickness.

    We returned to our childrens walk in centre only to be told the same thing.. “gastritis” again she was prescribed a stronger form of antibiotics only for her not to take down again.. then the motor neuron issues took place. Sienna was showing clear signs of balance issues and could no longer walk/crawl/sit upright. She was very lethargic and hot. We went to A&E for the third time just to be told her immune system was weak and that some babies take longer to recover than others.

    Weeks went by while she rapidly reclined. She was soon stuck in a corner of the sofa watching TV and sleeping all day. We tried to contact our health visitor but she left the service and forgot to transfer her notes over to the new health visitor who didnt know she existed. I came to the end of my tether and broke down to the lady in the weigh in clinic who took my concerns seriously. She refered her to paediatrics but we wasnt going to be seen until June.

    7th of May came, I rang 111 (emergency service information) because Sienna couldn’t lift her head from her shoulder and was struggling to straighten her back. I was told to wait for a phone call of a paediatric doctor. They finally rang back 2 and a half hours later. They asked if she was still tilting to one side. She wasnt. So they told me to keep an eye on her and bring her in if she did it again!
    Friday the 10th of May 2019 Sienna fell off the sofa. She bumped her head and her eyes rolled back. I didnt bother phoning. I took her straight in. I lost all faith in the emergency phone services/GP/Health visitors. When we arrived then again didnt believe what I was saying, when she was too poorly to move and her cry was weak. Eventually the most amazing doctor came and spoke to us. She listened to everything. Even wrote it all down. She measured Sienna’s head and demanded an urgent MRI. 
    11th May 2019 We had our diagnosis. Within 2 hours of the MRI. We was taken to see the consultant. He broke the news Sienna has a tumour just a slight bit bigger than a golf ball in the back of her brain. We were heart broken. She had an external shunt fitted to drain the mass of fluid on her brain. In 48hrs they collected 650ml of spinal fluid from her head stabilizing her condition ready for her operation 14/06/2019
    Surgery day came, they’ve so far removed what they think is all of the tumour.. 

    17/05/2019
    We had the results! Had a meeting with the consultant..
    This Mama Knew Something Wasn't Right
    This Mama Knew Something Wasn’t Right

    Good news – They’ve gotten rid of 95% of the tumour. 
    Bad news – Its defiently a stage 4 aggressive medulloblastoma. The 5% that remains is attached to a membrain that the surgeon didnt want to remove as it would effect her brain development. In two weeks time she will have chemotherapy.

    We expected this outcome.

    Still doesn’t stop the pain, anger and emotion. I know she is a strong ass girl who will kick cancers ass! 

    I want to raise awareness about the earlier detection of a brain tumour especially in children. Because nobody should have to suffer what Sienna-Rose did! For months she was miss diagnosed. All it takes to diagnose is an MRI brain scan! Here are some symptoms to look out for..
    – Involentry eye movement
    – Tilting of the head 
    – Growth of the head 
    – Vomiting and nausea 
    – Lack of interest in food 
    – Poor movement 
    – Behaviour changes 
    – Unable to hold balance/Regression in milestones!Even if you think it’s not.. request to be seen my a neurologist to rule out a tumour! Earlier detection means better treatment and a higher survival rate! Trust your gut instincts and if you feel something is wrong, please fight until you find out what is! 
    – Sienna-Rose’s Mum xx

     

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  • Can You Help Save A Police Officers Life

    My name is Helen Rayner, I am a publican in Hounslow, west London. I have two daughters 30 year old Jade and 25 year old Amber I am also grandmother to Jades 5 year old daughter, Eva. Jade is married to Gareth who is ex military and now a fitness instructor. Jade is a serving officer in the Metropolitan police force. Life was looking good, they were about to buy their forever family home and turn it into their dream place. Then, overnight, their dreams turned into a nightmare.

    In February of 2017 Jade was diagnosed with stage 3c triple negative breast cancer which for those of you that don’t know is a rare and aggressive form of cancer which had already spread to her lymph nodes. Well as you can imagine we as a family were all blown away by this news with the exception of Jade whose attitude towards it was ‘OK, I have it lets get on with it’.

    Months of aggressive chemotherapy, surgery and a good hammering of radiotherapy followed yet all the way through Jade was amazing and an inspiration to us all. Not at any time did she complain or whinge, not even when her hair started falling out, she just reached for the clippers and took control. Her sense of humour never faltered and, to be perfectly honest, helped the rest of us through. Her whole focus was on beating this disease and getting back to work and continue with her life.

    The day Jade was given the news that she had had a complete pathological response to treatment (the all clear) she left the hospital like her backside was on fire. Her mother literally had to run to keep up with her!

    In February 2018, as soon as the doctors permitted, Jade returned to the job she loves albeit on recuperative duties slowly building up her hours with a view to return to full duties in September. But, in late May Jade began suffering from a persistent headache, she just couldn’t shift it. By the first week of June she could stand the pain no more and took herself to A&E. Jade insisted on a CT scan, after revealing her recent medical history they finally agreed to do it. Sadly the results of the scan revealed several masses to Jades brain that were suspected to be the breast cancer that had metastised. Further scans, an MRI and PET resulted in the following diagnosis:

    Stage 4 Brain Mets a Total of 7 Tumours

    Yes you read that right…..7 metastatic brain tumours. Due to the location and number of tumours surgery to remove them is not an option in the UK.

    Jade was referred to the Royal Marsden hospital in London where they performed 3 sessions of stereotactic radiosurgery (the cyber knife). They treated all 7 tumours in a bid to shrink them as much as possible. If this treatment is successful it will buy Jade some time but we wont know how the tumours have reacted until September 2018 when she will be scanned again. In the meantime we are trying holistic therapies, diets and anything else that may help. Then there is the relentless search for treatments in other countries.

    In the UK Jade has been given 12-24 months to live, yet in the USA, with the right treatment, people are living for many years with their cancer being classed as dead or sleeping.

    We have met with a young woman from the UK by the name of Melissa Huggins who 10 years ago was also given 2 years to live by doctors in the UK and, like us, Melissa’s parents refused to accept the prognosis and took her to the USA for treatment. 10 years on, Melissa is now married with a young daughter. She has no idea if her cancer is dead or sleeping…..but shes still here.

    We have found a fantastic clinic in the USA, Duke Health, that believe they can treat Jade, they are currently working on a care plan for specifically for her. But this is going to cost, we are not sure as yet of what that will be in terms of money, but there is no price too high to put on such a sad waste of a beautiful life and the devastation and loss that would ensue should we not achieve our goal and GET JADE WELL so she can watch her daughter grow into as wonderful a woman as her mother is.

    As a police officer Jade runs towards danger to help others, now she needs others to help her to be here for Eva.

    Please help Jade here https://www.justgiving.com/crowdfunding/justjade

  • A Routine MRI Ended Up With My Baby Having Brain Surgery

    August 2016 my beautiful little baby boy went for a routine MRI, this was to check this was to check everything was ok due to him being born early at 31 weeks and his first 3 months were touch and go.

    We had expected it to be an in and out appointmen…IT WASN’T!

    Before he had come around from the sedation the doctors came into the bay, pulled around the ‘sound proof curtain’ and delivered the news that my tiny baby boy had a huge build up of fluid on his brain.

    A blow we were not prepared for! How do you cope with being told that the tiny baby laying in front of you has something seriously wrong with him, a baby wh no chance to live.

    We had 5 months of calm our baby boy was a perfect addition to our little family and his big sisters doted on him and then it’s like everything around you shatters.

    We had to prepare ourselves to watch our baby face something we knew nothing about, we had to tell our young daughters that their much-loved baby brother had a poorly head and the doctors had to make him all better, they were too young to understand but I could see they were worried.

    The next day he was taken to Addenbrooks where he would spend nearly a month!

    We were presented with the choice between a shunt or ETV (endosopic third ventriculostomy) a hard decision and we followed what we thought would be the best long-term solution along side the advice from his neurosurgeon.

    After 3 and a half hours we got the call that our tiny baby boy was out of brain surgery.

    The ETV had failed he now had a bleed on the brain, seeing him laying there with a tube coming out of his head and blood filling up the pot that it was attached  was absolutely heart breaking, if I could have swapped places with him I would have.

    Our daughters were amazing throughout all of this, we didn’t want to scare them and let them see their little brother with a tube coming out of his head and them not being able to pick him up but they got tearful not having him at home with them, they had moments of being sad but they kept us ‘distracted’ and helped us to keep going forward.

    Our little fighter had to have an external drain to relieve the pressure and to allow the blood to clear, brain surgery 2 was 9 days into this to replace the tube and reduce the risk of infection.

    It took 3 weeks for the blood to clear and then it was time for his 3rd surgery to place his shunt, he was home the next evening!!!

    The shunt drains the fluid from his brain to his abdomen.

    To look at you would never know he had it, it just means we have to be extra cautious with his head and any type of hit to the head could end up with him back in hospital for more surgery.

    When he is poorly or sick it puts us all on edge as not only is it horrible seeing your baby ill but sickness is also a symptom of a malfunction.

    As of August 2016 our boy has hydrocephalus, a chiari malfunction (the route cause of hydrocephalus)and epilepsy.. these join a list of problems he’s had to face and continues to.

    A Routine MRI Ended Up With My Baby Having Brain Surgery
    Our little fighter now.

    But he is our little superhero! He’s battled a lot and has come such a long way.

     He is always happy and such a character, your typical boy who loves cars, dinosaurs, paw patrol and being on the move non stop.

    Shunts are far more common than I ever realised and they save lives, I thank my lucky stars every day for the person who invented the shunt without it our boy would not be with us today.

     

     

  • My Baby Has An Inoperable Brain Tumour

    This is Edie Molyneux, she is three years old and was recently diagnosed with an inoperable brain tumour, her only chance for survival is a hospital in Mexico who have a number of success stories through this condition.

    She has a condition known as DIPG, Diffuse Intrinsic Pontine Glioma, commonly referred to as pontine glioma, infiltrative brainstem glioma, or DIPG, is a rare tumor of the brainstem that occurs almost exclusively in children. A pontine glioma occurs in a most delicate area of the brainstem (the “pons”), which controls many critical functions, including breathing and blood pressure. Its location, as well as the way it infiltrates normal brain tissue, makes it especially difficult to treat.a rare cancer affecting children.

    Which in Edie’s case is a tumour in the centre of her brain, making it unreachable by uk standard methods without poisoning her whole body, this is where Mexico come in, they have the advancements to treat and shrink the tumour and have 2 cases of No Evidence Detected in other children.

    However we need to raise £300,000 to make this possible, every share, awareness raised and £1 means the world to us.

    Here is a photograph of Edie and a scan photograph of her tumour, also a link to her fundraising page, thank you ever so much, your support will be eternally appreciated.

    Come on Mums advice ladies lets help this little girl, how much do you pay for a bottle of wine or a chocolate bar? Every pound could make a huge differnce and save this precious angel https://chuffed.org/project/the-spider-ede-appeal

    A Chrismas Miracle is what we need

    All my love,

    Emma Fessey

     

    My Baby Has An Inoperable Brain Tumour

     

     

  • My Husband And His Energy Drink Addiction

    Brianna and Austin were so excited to meet their new baby boy. 

    But one morning, Austin’s mum phoned with life changing news.“Austin had an accident” she told the worrier mum to be.

    After a long drive to the hospital, Brianna learned that Austin had had a brain hemorrhage.

     But the reason behind the sudden horror was just as unexpected.

    Austin had been drinking energy drinks ever since he’d started picking up over time and had to commute more regularly.

    Brianna learned that Austin had had a brain hemorrhage. But the reason behind the sudden horror was just as unexpected.

    It became a regular habit and soon, Austin was drinking them excessively. Doctors say they’re ultimately what caused Austin’s brain hemorrhage.

    Brianna said Austin had to have a lot of brain surgery to save his life, everyone was terrified. 

    Following this were strokes, seizures, swelling, and more things we weren’t prepared for.

    “Then the time had come for me to deliver our baby”.

    “I’m not going to lie to anyone, it was so hard. I had planned on Austin being a part of this huge moment. Being by my side. Holding my hand. Being there to cut the cord. Being there to welcome our son into the world. It didn’t feel right”.

    “But a beautiful miracle happened as I delivered our son. Austin woke up”.

    Austin was still too weak to see his son and was in and out of consciousness.

    Brianna said ” At a little over 2 months old, our son finally met his dad. A day I wasn’t sure I would ever see. That was the day that my heart gained some of its happiness back.

    Some time after that he could finally come home to me. Our life isn’t normal. There are doctors visits and hospital trips — so many that I lose count”.

    “But we are here. Fighting”.

     My Husband And His Energy Drink AddictionMy Husband And His Energy Drink Addiction

      

     

  • Cancer Made Me A Single Dad

    My story So some quite a few years ago I met my lovely wife, as time went on I knew she was definitely the lady for me.

     She had often said she wanted children, to me I wasn’t fussed either way.

    Shortly before going on our holiday my girlfriend Stacey said she was going to the doctors as she has something weeping from her nipple. So she went to the doctors and was told not to worry it’s just an allergy, and to put some cream on it and perhaps change our washing powder.

     She had a sigh of relief and off we went on our holidays. On our return she without me knowing did a pregnancy test and found out she was pregnant. I wasn’t over fussed but she was happy. 

    As the time went on she was having a number of issues, bad back pains, leg and hip pains and starting to hunch over a lot so went to the doctors, and we were told she’s just one of the unlucky ones who’s having a bad pregnancy, she was sent to physio etc.

    A few weeks later a lump had formed on her left breast which again she had checked out by the doctor and was told it’s just a blocked milk duct you just won’t be able to breast feed. 

    At the time I was working away a lot so she had to go to either her mums or sisters as she was struggling to do things on her own, I was helping her shower. 

    We did all our scans as you should found out by the nurse blabbing that we were having a boy which I was a bit more excited about if I’m honest.

    Then we were at home and she went to the toilet and saw some blood in it so went off to hospital, we were told that her waters had broken at 21 weeks. 

    We were then told our hospital was not kitted out to deal with a baby that premature so she had to be moved to Luton hospital and monitored.

     There she was for 2 weeks constantly being monitored and checked, after the 2 weeks she was discharged and we were told that yes the waters had broken but only a small amount of fluid had escaped so all was ok.

    I returned to work that weekend, to get a phone call from Stacey’s mum saying they had to take her back to hospital and the hospital think she has got pneumonia.

     I asked if I should leave work straight away but they said just come back in the morning as usual. The next morning I went to Stacey’s mums before going to the hospital, by this time she had been moved to intensive care ward. 

    I came in and saw she had been put in to an induced coma and they had been doing tests on her. 

    After a few hours a doctor and nurse came and saw me and said that they found Stacey had breast cancer, which had also spread to the glands under her arms her lungs, and all of her bones causing 2 vertebrae in her neck to collapse. This aggressive amount of cancer had spread so far because of her being pregnant.

    They then told me that they need to give her chemotherapy there and then and needed my permission to continue. I was not sure what to say as we weren’t married at that time, but they said if I didn’t she would definitely be dead within a weekend, I asked about the baby and they said that they have done it before but as it stands Stacey was here and the baby wasn’t. I agreed and they gave her the treatment. 

    After a few days she was still going down hill on a breathing machine, they said they wanted to try giving her a tracheotomy (putting a breathing pipe direct in to her wind pipe ).

    This seemed to help and gradually she improved, all the time still pregnant.

    Eventually the doctors were saying about delivering the baby at 30 weeks while she was still in a coma. But they ended up not doing that. 

    She was then revived and we had to give her the news of what had been going on. 

    After a few more weeks she was stable enough to be moved to the cancer ward.

    They were also  saying that they wanted to deliver the baby and finally made the decision to do so on April the first, however my baby didn’t want to be born on April fool’s day so Stacey went in to labour on 28th march.

    We were shortly moved to  a maternity ward and we were taken up to delivery at about 7am on march 29th. She was told she had to have a Caesarian as her body couldn’t deal with a normal birth. 

    I was allowed in as Lind as the epidural worked which it did, so there we were and out came our little boy about 7 weeks early weighing 4lbs exactly. We chose his name Thomas and off he went to baby intensive care.

    After Stacey was stitched up and sorted we went to see him, we were told he would be on a breathing machine for about 2 days but he was off after about 2 hours!!

    As the weeks went on I would take Thomas from intensive care over to the cancer ward and also take Stacey over to see Thomas, eventually we were all allowed to go home on the same day. 

    All was great Stacey had fought off all the cancer except for in her bones which was being managed by regular treatment. Thomas was growing and doing fine then after about a year Stacey started getting headaches so we went to see the doctor to be told that she had secondary cancer on the brain which they might not be able to do much with. 

    We were managing but arguing a lot because of all the medications she was on. 

    Rapidly approaching was our wedding day and Stacey was really upset she lost her hair again just before getting married. Then on the week before we were getting married I was mugged I had my head stamped on etc so had to wear make up to my wedding haha! 

    It all went great, but over the next few months Stacey started having nose bleeds and fits etc..

    Finally she was taken in to our local hospice for what I thought was rest bite but once she was there I found out they were stopping her medication as it wasn’t doing anything they would just be giving pain relief, they expected her to be there for just a few days. But after a few weeks I started to think they must be wrong, but I was, on the 9th week of her being there I arrived and I had been there for no longer than 10 minutes and she passed away 10 days before out 1st wedding anniversary. Thomas was 2. 

    Thomas is now 8 it has been very hard for me especially when he’s upset about missing his mummy. But we get through it.

    I’m not looking for sympathy. I just hope my story will educate people of some of the early signs of cancer