Posted on November 07, 2019 by Amber Moon
As someone who had primary breast cancer and then diagnosed with secondary incurable breast cancer, I wanted to show my support for this campaign as Fiona and her team have helped me every time I have been away on holiday.
Posted on August 14, 2019 by Amber Moon
Chemo bells are a controversial topic with very split opinions. Heidi (@storminatitcup) spoke about the subject on her blog not too long ago and it instantly struck a chord with us. So much so, that we decided to join in on the discussion. Read more
Posted on April 03, 2019 by Amber Moon
Things don’t always quite work out as planned. Can you believe that? Don’t know about wool over your eyes, I must have had a whole sheep.
The biggest part of (my) life is figuring that out and being ok with it. Despite (or in spite of having EDS) I am a pretty energetic soul. I spend this time volunteering and donating my experience and expertise to charities and social enterprises. Sharing the wealth is something I have always believed in – particularly as I was raised on a council estate by my single dad. As such, my grandparents wrapped a lot of love and time around us – they injected a huge dose of love into our community via running the Scout Group, (WORD) workshops and craft classes and acting as an extended family to many. Last year a road was named after my Grandad in our village. I’m pretty proud of that.
This investment in the people around me fuelled my spirit and helped me make a heap of friends – some of the kindest folks I’ve ever met. It also contributed to my burnout and I was in total denial. It was if I thought if I keep going things will be ok, I’ll be back to normal any time now. And they are (almost) and travel has played a huge part in that. Depression and anxiety creep up on you, like a fog; descending to rest comfortably on your shoulders.
Me: Oh hey
Fog: Imma sit her for a while, you ok with that?
Me: umm, sure.
*three years later*
Me: So, about this free ride..
I’ve travelled to some incredible places, like Vietnam, Cambodia, Australia, New Zealand, Copenhagen, Tonga and culinary roadie across Italy to name a few. However, my spiritual home is New Zealand and I am back here with an aim to heal and reconnect. In the fog of depression, it’s like you’re doing stuff you think is right, but on reflection, it’s not. Working through that is hard, but necessary.
I am a big fan of Matt Haig and his book Reasons to Stay Alive made a huge impact on my recovery. In the spirit of his amazing book, here is my fuel and love list:
I was diagnosed with Ehlers Danlos Syndrome when I was 11. It’s a genetic connective tissue that manifests itself in many different ways – making it pretty hard to diagnose. Depending on which type you’re diagnosed with (there are several different classifications) you might experience anything from joint dislocations, aortic dissection, Raynaud’s Phenomenon, valvular heart disease, atrophic scarring and the early onset of osteoarthritis. There is no cure for EDS and most people will receive specific treatment for their specific symptoms.
I have experienced a bunch of different bumps in the road with EDS and I count myself lucky that I have not had had a seriously life-threatening moment. With Classical EDS, my main issue is healing and recovery. Sprains and dislocations take ages; my skin tears like tissue paper and then when it finally heals it looks like I’ve scrunched that tissue paper up like rubbish. Annoying and slow, but not debilitating.
When I see campaigns that amplify ’love the skin you’re in’, I find myself thinking back to my teenage years, when I refused to wear anything but trousers and 100 denier tights, even in summer. The scars on my legs had left such a profound dent on my confidence, that I hated the way I looked often refused to have photos and do the things I loved – like performance art, netball, swimming and dance. God forbid anyone sees my hideous legs. I often wonder how social media would have impacted me back then. Would I have followed #EhlersDanlos on Insta and realised I am not alone and not weird and broken? Perhaps. One thing I know about the positive power of social media is the community. The love that can pour out of people feeling the same thing.
My main challenge is saying no. I love to travel and jump and climb but that’s a bit of a challenge when your skin splits open like a peach if you graze it. I have to reign it in most of the time and more often than not it pays to plan ahead and see how my EDS can be accommodated.
In 2018 I jumped on a plane to Tonga and spent a week on a wee island a short boat ride from the main island. This was my first solo trip so far away from home. It was also the first time I snorkelled and kayaked around a coral reef. Long may these ‘firsts’ continue. For me, this is huge progress in healing and recovering from almost two years of depression and anxiety.
Posted on April 01, 2019 by Amber Moon
During remission, it is important to take time for yourself to allow for healing, both physically and mentally, with spas being an ideal place to do so. However, statistics suggest that as many as 97% of spas turn those with a history of cancer away. This is shocking considering that one in two of us will get cancer at some point during our lifetime.
This being said, there are some fantastic remission retreats around the world. These are designed to support guests, providing a space where they can begin their journey of healing and recovery. Read more
Posted on March 29, 2019 by Amber Moon
My name is Emma Rayner. I am a wife and a mother to two beautiful boys aged eight and four. I help run the Lucy Rayner Foundation- a charity particularly close to my heart. We raise awareness and provide support for young adults with mental health challenges. The charity offers services including; free counselling, support groups and monthly informal coffee mornings. No one should ever feel like they’re alone, so we do everything we can to make a difference in young individuals’ lives. Read more
