Back in 2006…
my daughter was diagnosed with Type 1 Diabetes at the age of 3.5yrs – it was devastating at the time. Whizz forward 18mths and she was diagnosed with Coeliacs at 5yrs old – double whammy! I brought loads of books to ease my transition into the world of GF … guess what, I’ve sold them all since, you heard me, every single one of them! I use ‘normal’ recipes and adapt them. More recently my little boy has been diagnosed with Anxiety. As you can see, we’re your average run of the mill family with a few dramas rolled into the mix.
The idea of a blog had been ping-ponging around my mind for some time. People kept telling me I should write a book or something similar, maybe something to illustrate the complexities of life with a Type 1 Coeliac child. I love to educate people about Beth’s medical conditions and I share these thoughts, wishes, trials and tribulations on this site with the very best of intentions. I take no pleasure in offending or upsetting anyone and trust me, no one is a bigger judge of me than ME. My ramblings are simply this; a reflective account of what’s been, what going on now and what the future might hold because after all, life is a drama!
So, I’m Rebecca and I’m a stay at home mum, married to my childhood sweetheart Brett whom I met at 15yrs old! Brett is an absolute rock, his ability to allow things to bounce off him amazes me and he has supported me leaving a career to focus my priorities on our children. You see, I gave up a 15 year career working with young adults when I had a spate of …. lets call it anxiety. The fact is, I was spinning too many plates at once and during my time off work ill, six months to be precise, I gradually came to realise that being a mum was my primary job, my children needed me to be 100% well in both mind and body and have the strength to guide them through each obstacle course.
Bethany (born 2004), has Type 1 Diabetes (diagnosed 10.04.08) and Coeliac Disease (diagnosed 18.08.2009) and also struggles off and on with a condition called Pica. She’s the most amazing girl whom despite all her medical woes, seems to shrug them off in a matter of fact, who give’s stuff kind of manner, I love her attitude and see so much of me as a a teenager in her, I’d love her to keep it, it’ll serve her well in life.
Lewis (born 2006) is the ying to Bethany’s yang. He’s my sensitive little chap who absorbs people’s woes and anxieties and struggles as a result. Lewis was diagnosed with Autistic Spectrum Disorder in 2016. It’s still very early days in his diagnosis and although we’ve naturally adopted coping mechanisms over the years without realising it, we’re learning about Lewis’ ASD every day. Both children have conditions that often leave me feeling an extreme lack of control, and control something is feel I must have in order to cope!
This site and my blog began as part of my self therapy, I was exhausted spinning all those plates. With the strong urge to regain some control within this drama I decided that my fingers could help to alleviate some of that negative energy, even as I type now, beating down on the keyboard, I can feel an element of calm wash over me, and that can’t be a bad thing can it?
We’re called Glutarama because the gluten free baking is actually the happy ending to each drama, whilst some may be pulling their hair out over perfecting the worlds best gluten free Victoria Sponge, I simply love to bake, like tapping away on this keyboard I love to beat an egg, cream butter and sugar or pound bread… who needs electronic gadgets and gizmos to do all the hard work when you’ve got plate spinning energy in your arms! And whilst that may sound selfish, that the baking is MY release and MY therapy, who can argue with the heart lifting scenes of children licking the spoons and bowls and eating the biscuits, cakes and other such goodies before they’ve barely cooled down!
So, if you’re interested, come follow me and my family in the challenges and toils of Type 1 Diabetes, ASD and Coeliac Disease. Marvel at my my baking successes (I do!) giggle at our little adventures (I promise I’ll always end a post upbeat, no matter what the subject!) and take comfort in the that fact that we’re just your non-average family dealing with non-average challenges…because no one’s truly average right?