Welcome to my blog, feel free to follow my journey below.

Hi, I'm Shahn!

Hi, I’m Shahn. I’m 32 years old and based in the UK. I was diagnosed with Noonan Syndrome (NS) at birth, a condition that has shaped my life in many ways. Over the years, I’ve undergone numerous operations and faced many challenges. You can learn more about my experiences in the ‘Living with Noonan Syndrome: My Journey So Far’ and Blog sections of my website.

While Noonan Syndrome has undoubtedly presented challenges, it does not define who I am. I’ve always believed in overcoming obstacles, and I continue to embrace life with resilience and a positive outlook.

This website is a platform for me to share my personal story and raise awareness about Noonan Syndrome. Through my experiences, I hope to shed light on the medical conditions, physical challenges, and other battles that come with living with NS. My goal is to help others understand the condition better and provide support to those who face similar challenges.
Thank you for taking the time to read my story. I hope that, by sharing my journey, I can make a positive impact and encourage greater understanding of Noonan Syndrome.

Living with the Physical Aspects of Noonan Syndrome

Having the genetic condition Noonan Syndrome (NS) presents a wide range of challenges, particularly on the medical front. Over the years, I’ve experienced many of the health complications commonly associated with NS. However, I’ve been fortunate when it comes to physical features—many of the more visible traits are either subtle or have changed over time.

As a child, my shorter stature was more noticeable compared to my peers, but by my mid-teens, my growth had caught up, and I now appear to be of average height. Physically, I do have some characteristics associated with NS, such as a slightly different nose shape, a tendency to bruise more easily, and a lazy eye with reduced vision, which has meant wearing glasses for most of my life.

In addition to these features, I also experienced some developmental delays, which are common among individuals with Noonan Syndrome. These challenges have shaped my journey, but they’ve also given me a deeper understanding of resilience and self-acceptance.

Unfortunately, not all of my experiences were shaped by the condition itself. From the moment I stepped onto the school grounds in high school until I finally left in Year 11, I was relentlessly bullied. This was one of the most difficult periods of my life, and I open up more about it in my next blog post.

If you’re interested in learning more about the physical characteristics and the development issues of Noonan Syndrome, I’ve included a helpful link at the bottom of this page.

https://www.noonansyndrome.org.uk/faqs/puberty-growth

https://www.noonansyndrome.org.uk/faqs/facial-features

https://www.noonansyndrome.org.uk/faqs/neurology

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