I’m Claire. I’m a vet and live with my husband, Mark in the North East of Scotland. I was diagnosed with Addison’s 2 years ago. We also live with our Jack Russell terrier, Monkey, who also has Addison’s. She was diagnosed 6 years ago and hasn’t let it slow her down.

I would like to raise money for the ADSHG because they have been such a valuable help since being diagnosed. From support during the early days to advice for travel, sickness and exercise. Their work is so important to all those living with adrenal disease. The training has been going well until I sprained my ankle and have had to take a bit of a break from running.

I’m Mark and I’m supporting my wife, Claire, who was diagnosed with Addison’s nearly 2 years ago. We both like climbing hills and riding bikes but we’re not runners. So training has its ups and downs.

Claire found the ADSHG really useful after her diagnosis. So I’m keen to raise some awareness and support for what the charity does. I’m currently able to run 3 miles a couple of times a week. It’s hard because the days are short in Northern Scotland so all our training runs are in the dark just now. I’m hoping to maintain this level for now and then start to do more as the days lengthen.

I was diagnosed with Addison’s disease on 1st April 2021, after being unwell for quite some time. I’ve found it really hard to adapt to having this lifelong disease, however, I want to prove that having the diagnosis doesn’t mean your life is over. I am not a natural runner, in fact, I get out of breath by just running up my stairs at home so this half marathon is going to be a huge challenge, with the added complication of Addison’s on top of that.

When I say I am a couch potato, I really mean it. I haven’t done any exercise for years. I started training 10 weeks ago and had to pause training due to being hospitalised. In my last run, I managed to run 23 minutes - I have a long way to go but with determination, I will get there!

When I was diagnosed with Addison’s disease 12 years ago, I was very grateful to have the ADSHG to turn to. I previously knew nothing about adrenal insufficiency! I spent the first 6 years of MY diagnosis still unwell and struggling but once I found the right treatment regime tailored specifically to me, I can now live life fully!

I started running regularly at the beginning of 2023. Running two half marathons in 7 days (Reading is one week after LLMH!) next year for the ADSHG will be a huge challenge! With their advice on updosing for exercise and support hopefully, I will be successful. Wish me luck!

I am raising money for the charity as my mum was diagnosed with Addison’s in June 2022. I am 22 years old and enjoy running and going to the gym. The ADSHG has been a great help and source of information to my mum since her diagnosis. She attended the AGM this year and has gained a lot of knowledge from the website and forum. My mum is so strong and I am so proud of her. She is the most selfless person I know and will always put others first. This diagnosis has changed all our lives. Mum copes really well but can never forget that she has this condition and has to listen to her body and make adjustments when needed. I can't wait to do this for my mum as I want to make her proud but also raise money for this amazing charity that has given us so much guidance and help through her Addison’s journey.

I have been running infrequently for the last 3 years. I have been very inconsistent with my fitness but I am determined to race a strong time in April. My main goal is to run a sub 2-hour half marathon, which would take a huge chunk of time off of my personal best.

Hey! I'm gearing up to run the London Landmarks Half Marathon on 7th April and it's not just about the miles for me. I'm lacing up my running shoes to support the Addison’s Disease Self-Help Group in honour of my incredible wife, Becca. In 2021, she faced a pituitary tumour, showing immense strength throughout. Now, she's tackling life with adrenal insufficiency. Becca, an amazing mum to our daughter, has worked non-stop throughout it all. Adrenal insufficiency isn't a walk in the park and the ADSHG has been our guiding light since her diagnosis.

So, here's the deal: I'm hitting the pavement to raise funds for this awesome charity that's been a lifeline for us. Their support means the world, helping improve lives and spread awareness about Addison's. Let's make each step count!

Initially, I wanted to support this charity as my Mother-in-Law has adrenal insufficiency as a result of brain tumour surgery in 2011. However, since signing up my 18 year old niece has been diagnosed with Addison's after spending 10 weeks critically ill in hospital. Both are dependent on replacement hydrocortisone and are at risk of potentially fatal adrenal crisis. I am so thankful that the ADSHG is there to help them both.

The ADSHG works to increase knowledge and support for the serious condition of adrenal insufficiency. Their support has and continues to save lives. I have taken on this challenge to support in raising awareness, as well as raising funds, for the ADSHG's very necessary work.