Glastonbuddy 2014

14 Aug 2014

Well we’re now back from our Summer holidays and I thought it was about time I wrote a post, so here goes…A week and half ago we packed up our car filling every single available space with camping equipment and headed off to Glastonbury – sadly a month or so too late for the festival!We broke the long journey and stopped over at our dear friends, Ric and Claire’s near Bromsgrove. Ever the perfect hosts and it was great to see their lovely son Ruben and Rosie playing so well together. Rosie certainly isn’t shy when it comes to meeting children she doesn’t see a lot of or indeed children she’s never seen before, this will be a valuable tool for her to take through life and I hope she continues with this confidence.So onto camping… remembering that Rosie is only three and we are still relatively new to having a child with DS I guess it’s normal (or at least I hope it’s normal) to wonder and perhaps worry a little about how you will be greeted to places. Greenacres Campsite near Glastonbury was our destination and we couldn’t have been made to feel more welcome, we were treated with complete normality which is so important given that this was to be our home for the next week.Duncan & Mary who run the fabulous family friendly campsite had a genuine interest in our whole family and that normality is totally priceless to us. Alice (9) their daughter (shown in the picture below) expressed a huge interest in Rosie and over the the week became our Bud’s new best Buddy. Alice asked so many intelligent questions – so keen she was to educate herself and find out as much as possible about Rosie and what it’s like having a child with Down’s syndrome. She regularly took Rosie off to the play area encouraging her to get up on her feet. Alice is such a delightful young girl and we can’t thank her enough for the moments of respite she gave Karen and I as she looked after our Bud. We will most certainly be back to camp at Greenacres in the near future and wouldn’t hesitate in recommending it to any family.Rosie was no trouble going to bed and took to camping really well, we had done a few short trips first so knew she’d be okay but it still surprises me just how adaptable she is to environment changes.Breaking up the journey again on the way back home we treated the kids (and ourselves) to a two night stay at a luxury spa hotel in the Cotswolds. Rosie is being extra clingy and super demanding for Karen’s attention at the moment and I was a little apprehensive as to how it would work in the environment of a hotel. Not always the most family friendly of places!Rosie’s constant need for attention coupled with shouting and sometimes screeching in public is becoming increasingly harder for me to deal with. As usual Karen just takes it all in her stride but myself well, I’ve been having a few wobbles again. I’ve been battling with that mistake parents of children with DS often make – ‘Looking to the future’. I know it’s counter-productive but I can’t help it sometimes, rather annoyingly it’s in my nature to be a little anxious. I keep thinking to myself is this Rosie from now on? Will this be our life, constantly worrying everyone’s tutting or feeling sorry for us? I’m sure its just a phase but it consumes me at the moment.Whilst getting ready for dinner I took the kids to the bar area giving Karen time to get ready without Rosie’s constant need for her. For the first time in a long time I felt that wobble come over me as I struggled to contain her neediness, screaming and crying for Mummy. I took her outside held her and cried. I know all of this is contrary to the blog title but I’ve always promised to be honest and yes for a moment there I stood and wondered if I can cope. Life isn’t always full of the Friday smiles, to be fair it mostly is, but equally there are moments that I struggle with.That said when we sat down for dinner she behaved impeccably and enjoyed dipping her vegetables in a sauce for her starters, showing signs of OCD with the dinner plate! (see video) – swings and roundabouts as they say.Tomorrow Rosie has her most important role so far where she is to be a flower girl at the wedding of our friends, Nicola and Brian. I can’t wait to share some photo’s of Rosie from the day. Table manners from The Future’s Rosie on Vimeo.


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The Future's Rosie

I'm Tom, a thirty something father to three beautiful children and husband to my soulmate Karen. I started this blog as a means to talk about stuff, get things out in the open, a bit like an online therapy I guess and to celebrate the progress of my beautiful daughter Rosie who was born in March 2011 with Down's Syndrome (DS) and a Complete Atrioventricular Septal Defect (AVSD). Maybe the experiences shared on here will help others too, hopefully help illustrate the bright futures our children with DS will have if we can break down common misconceptions. When I first found out Rosie would be born with DS I found reading literature with open and honest feelings on the subject, extremely helpful. This is not intended to be a written masterpiece and I can promise you it won’t be. I don’t pretend to have a large vocabulary and to be honest the further behind me my school days become the more my grammar has deteriorated!... however, you will find what is written on these pages comes from the heart.

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