1 in 17 people in the UK will be affected with a rare disease1. I am number 17 is a campaign to help the voices of those with a rare disease to be heard.

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This campaign is initiated and funded by Takeda.

Statistically speaking, I’m sat on your bus to work every day; I’m out keeping active on a Tuesday; I’m there when you’re grabbing last-minute dinner ingredients from the supermarket. Who am I? I am the 1 in 17 people in the UK affected by a rare disease at some point in their life1. I could be on my way to yet another appointment with a perplexed doctor, or just back from a world record attempt. I could be the parent of a child with a rare disease, learning to deal with the complexities of my child’s condition. Or I could have the most perfectly blended eyeshadow, which I nailed despite my arms being too weak to raise more than an inch.

I might have tuberous sclerosis, hereditary angioedema, Ehlers-Danlos syndrome, or any one of a myriad of conditions you’ve probably not heard of. Don’t worry, hardly anybody’s heard of my condition. I might have a rare disease or one that is extraordinarily rare. Whilst my experience gets shared with my family and friends and people similar to me, it’s not been shared much beyond that.

I am number 17 is a campaign to help the voices of those with a rare disease be heard, brought to you by Takeda, together with rare disease patient groups from across the UK. Our goal is to increase the understanding of what it is like to live with a rare disease and show that rare isn’t always that rare.

Helping spread the word are #IAmNumber17 changemakers, each with their unique experience to share.

Meet the changemakers

Alan's portrait


I live in a very small village of 17 people, so I am that 1 person out of 17 who lives with or is affected by a rare condition.

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A whole village came together for my lymphoma journey, and I wish this same village was present in my sickle cell days.

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Chloe and Ronnie portrait

Chloe and Ronnie

I would like to raise more awareness of the different rare conditions and make it easier for people to get diagnosed, so you don’t have to wait so long and fight for everything.

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David portrait


I have occipital horn syndrome. I call it OHS, it’s ultra-rare and I’m the only person in the UK living with it. The disease affects every aspect of my life.

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Emma portrait


I want to be part of representing disabled people, help create inclusion and diversity. I want to be a role model I wish I had when I was growing up with my disability.

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Jack portrait


After taking up swimming at the age of four, I never dreamed that I’d end up representing Team GB at the London 2012 and that it would be the best experience of my life.

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June portrait


I was diagnosed with sickle cell, a genetic blood disorder that affects the red blood cells. My loved ones are an essential part of me getting through this disease. I am one of the 17.

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Karen portrait


I have lived with Hereditary Angioedema (HAE) all my life, I was born with it, and was symptomatic from about 2 years old. When I was diagnosed, I didn’t know anyone else with the same condition as me, which was rather challenging.

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Lara portrait


It would be so wonderful if I went up to someone and said I have EDS and they didn’t say ‘what’s that?’.

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Lucinda and Nola portrait

Lucinda and Nola

It would be brilliant if there was more awareness of rare diseases and an increase in public understanding. I used to be one of those people; I was unaware.

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Mel portrait


They thought I was okay at first, but by the time I was 6 months old I couldn’t sit up. As I got older, I got worse. I had two beautiful girls, but as soon as they were old enough, I taught them to hang on to me, rather than picking them up.

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Nicola portrait


I live with Feingold syndrome. I suffer from the shortening of my fifth finger that curves inwards, and also have webbed toes. I was often bullied at school because of them.

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Prabhjot portrait


Once you tell people that you have a rare disease, they start treating you differently. They start feeling sorry or pity for you. Although, we truly appreciate their support, that’s the last thing we (living with invisible disease) want.

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Rachel portrait


I received my Ehlers-Danlos syndrome (EDS) diagnosis at the age of 21. This is the first time I’ve ever been this open. The reason I’m putting myself in this vulnerable position is so awareness increases about rare conditions.

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Rebecca and Hannah portrait

Rebecca and Hannah

Hannah’s primary diagnosis is Inv Dup Del 8p, a rare genetic condition with only 65 known affected worldwide. She is also a daughter, a sister, a granddaughter and Nana’s Hannah. She is a cousin, a friend, a student and a teacher.

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Sally portrait


I was diagnosed at 18 months old when I started to walk, so I’ve lived with X-linked hypophosphatemia (XLH) as long as I can remember. I always have some level of pain and stiffness; however, it can be manageable.

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Shona portrait


It is important to have as many voices out there as possible. Not one person is the same. People underestimate the value of using their own voice.

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Zainab portrait


On 28th February 2014, my son Adnan was born. Adnan was rushed to intensive care as soon as he was born. After a few weeks of multiple tests, the doctors told us he may have a rare genetic disorder called Mucolipidosis Type II.

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This campaign isn’t just about us – it’s about you. If you live with, or care for someone with a rare disease, share your experience on social media using the hashtag. Help us be heard.

This campaign is initiated and funded by Takeda and supported by:

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