There’s nothing better when visiting a new place than finding a local market to explore and uncover any treasures hidden amongst the stalls. Manchester proved to be no exception and we were tempted by the vast array of produce, handcrafted gifts and other knick-knacks on offer. G was drawn to the trays of sparkling jewellery, whilst M investigated the various food items to see if anything was M-friendly and worth considering. He was delighted with the fresh fruits on offer as well as the multiple flavours of Turkish Delight that seemed to be calling his name, whilst G was drawn to the jewellery stalls, particularly the rings. We found a variety of small items to pick up for future occasions, well Christmas is fast-approaching after all, but the out-and-out winner for the day has to be the amazing “Curry On Cooking” Korma curry kit
Company founder, Veena Josh was on hand on the market stall and more than willing to spend some time chatting to me about their curry kits, which are fantastically top-14 free and definitely worth a try at home with the children. G isn’t the biggest fan of curry, but M loves Indian food and I was hoping that this would give him a more authentic taste than the concoction I usually manage to scrabble together for dinner from whatever spices are lurking in the back of my cupboard. Veena shared with me that not only does each pack include a recipe on the packaging, but also either she or her sister try making their curries using a variety of milk alternatives to check that the curry can be prepared to be as allergy-friendly – and delicious – as you want and need it to be.
Having bought a kit and brought it home with us after the indoor sky-diving adventures, it was a case of waiting for the perfect opportunity to give the recipe a whirl and just a couple of weeks later, we decided on a curry for our Saturday night family dinner. M read through the ingredients listed on the inside of the pack, made a note of anything we needed to buy to make it and then helped prep and cook the meal itself. A delicious meal was prepared and served to our discerning family audience. M, Mike and I all very much enjoyed the flavours of the curry and whilst G was far more reluctant to give it a glowing review, she did manage to finish her plate,eventually!
The curry kit has since been used to make another dinner for the children as well as a handy safe alternative to the biryani spices needed for M to cook with at school. We will definitely be trying out some of the other curry kits available and seeing just how far we can push that spiciness factor!
It’s hard to believe that we’re already at the start of May, which means that in just 12 days time, it’ll also be the start of National Eosinophil Awareness Week 2016. For me, every year seems to follow the same pattern:
At some point in late February/early March I realise that #NEAW16 is approaching and think I probably ought to do something about it…
Mid-March arrives and I finally get round to discussing with M and G what they think we should do this year to raise awareness of EGID and might even make some notes…
April begins and I realise that time is flying past far quicker than I imagined it would and begin to mildly panic about getting started on our preparations…
End of April and, depending on what I’ve managed to arrange thus far, I suddenly go into full-blown melt-down and panic mode as I realise that the start date is just around the corner and absolutely nothing is ready!
This year has been even more hectic than usual and not just because of the additional efforts needed in coping with M’s broken leg and what looks to be a rather nasty flare-up of his EC as a result of it. Between the children and I, we’ve determined to make this year’s Awareness Week bigger and better than ever before, which meant starting much earlier than usual too. In the past week I’ve organised, arranged and pencilled in dates for various events and whilst some will be happening ahead of May 15th, there are others planned for the week itself. Our current plans include:
a stall at our local Scouts’ May Fair, raising awareness and money
an article in our local paper all about our plans and an update on where M is a year on since the last Awareness week
yet another interview on our local BBC radio station, who are willing and delighted to have me in talking all things EGID for the 3rd year in a row
M and G have written, illustrated, filmed and directed a brand new video for #NEAW16, which I will be posting a link to in due course
M is in discussions with his Headteacher and is hoping to have display boards up in the school hall or library during #NEAW16. He has also planned some lunchtime games to raise some money for Over The Wall, our chosen charity for this year, and wants to show his presentation during an assembly too
a stall at our local market at the end of #NEAW16, again an opportunity to get information out there about EGID as well as fundraising once again
Mike, G and I have all committed to “Eating like M” for the week, which is the first time that G has wanted to be fully involved and will require lots of inspirational cooking from me
Finally, I have committed to attempting to post a new piece of information about EGID, be that fact, photo or update, via my FB and Twitter feed throughout May – and have given fair warning that I’ll be doing so!
Over the next few days, profile pictures across FB and Twitter will slowly turn purple as those families living with EGID around the world start to raise awareness of this chronic illness. It won’t just be me posting facts and information to share with families and friends about how it impacts on everyday life, but others will be doing it too. So, if you see a post, or a blog, or an update that particularly resonates, either from me or someone else, please share it on and help us reach another person who has perhaps never heard of EGID before.
We have decided to support Over The Wall and their serious fun camps through our fundraising this #NEAW. If you’re able to donate even a very small amount, you can follow this link to my JustGiving Page and help us to help OTW make a difference to another child with a chronic illness and their family.