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On 4th July 2014, Robyn & I were thrilled when our beautiful baby boy, Noah, was born. The first 5 months of Noah's life were the happiest we have ever been.

Just before Christmas we took Noah to see a pediatrician, as we were becoming a little worried about his lack of leg movement. We expected to be told that he may need some physio, but to our utter dismay we were told the unbelievable news that Noah probably had a serious neuromuscular condition.  In early January it was confirmed that he has SMA Type 1.

SMA stands for Spinal Muscular Atrophy. It's a genetic disease that is currently incurable. One person in every forty is a carrier of the defective gene that causes SMA and if both parents are a carrier, their child has a 1 in 4 chance of having the disease.  In the human body, messages travel from the brain, down the spinal cord along motor neurons to the muscles. In a person with SMA, these messages can not get through. This means the ability to control the muscles gets less and less to the point where they get weak and waste away. SMA Type 1 is the most severe form of the disease and is generally picked up by the time a child reached 6 months. It is the biggest genetic killer of under 2's in the UK. About 80% of babies with SMA Type 1 sadly pass away before their first birthday. 

Currently Noah is very weak in his legs, back and neck and has limited movement in his arms, however SMA does not affect the brain at all and he is one happiest babies you could ever hope to meet. Noah has the most beautiful big brown eyes and the cheekiest smile you will ever see. He is always giggling and laughing and making funny noises. He is always chattering away! If ever we feel sad all we have to do is look at him for second, listen to him for a moment and he makes us laugh.

Every night Noah is looking forward to the morning and every day is his best day yet. Robyn and I are determined to stay positive and to enjoy every single moment we have with Noah. We are blessed to be his parents. 

When we were first told that Noah was poorly, we called ACT for SMA. The very next day Emma and Karl drove down from Lincoln to see us. Emma and Karl are the founders of the Ally Cadence Trust for Spinal Muscular Atrophy. They lost their beautiful daughter, Ally, to SMA Type1 six years ago. Following their experience they felt that parents with recently diagnosed children needed support and information quickly. They set up ACT for SMA to try and generate a new line of funding and to raise awareness of Spinal Muscular Atrophy nationwide and to provide support to affected families. Emma and Karl came to see us so quickly and spent hours with us, answer questions and discussing their experiences. They also brought with them a new travel system for Noah, sensory light weight toys for him, monitors and a camera. They advised us to start doing activities with Noah, such as going to the beach and the zoo, which we are now doing. They continue to provide on-going advice and support.  Without their help, myself and Robyn could not have coped as well as we have. 

Robyn and I are very lucky to have our families' close by and to have lots of wonderful friends. The support we have received has been amazing. So many people have asked how they can help and if there is a charity they can raise money for. We have had amazing support from the NHS, Diana Nurses and Rainbows Hospice, however ACT for SMA have been incredible and we would like to focus on raising money for them.

I work for Navitron Ltd and they have been so supportive. They have organised a trek up Snowdon on the 24th / 25th of April to raise money for ACT for SMA. Employees, friends and family have signed up for the trek, so hopefully we will raise a lot of money. 

ACT for SMA were there for us when we needed them, so please give generously, so they can be there for the next family who call them.