Wordless Wednesday: Purple Haze
Today didn’t start very well but it certainly ended on a high note! I was up less little more than an hour before having to take myself straight back to bed. I remembered to set an an alarm as I had an important date to make this evening! Having got up for the second time, I threw on some clothes, fed the cats and rushed off to get the train up to London to meet Simon and our friend Julia. Our destination was the beautiful Union Chapel venue in Islington for a 35th Anniversary screening of the film Breaking Glass.
This was followed by a Q&A with Hazel O’Connor, a performance with her band, Sarah Fisher and Clare Hirst, who were then joined by a full choir in front of an audience that really was packed to the rafters! I was able to copy a couple of images from my camera onto my phone to process on the train returning home. The rest of my photos today were taken on the phone, including a lovely one of me and Simon that Julia kindly took for us! Lots of interesting purples for #PurpleFriday including Heather’s dress 🙂
#EveryDayIsDifferent #7daysofIBD #crohnscolitis
I thought you’d all like these wonderfully different chrysanthemums to mark the third day of Crohn’s and Colitis Awareness Week. Purple is the themed colour for IBD awareness and I’m having fun with my purple blooms. These ones always make me think of a big, colourful firework exploding! I really enjoy the way those petals start drooping as the flower starts to die back. Such interesting shapes 🙂
Today I had a chat with a friend in Vienna who also has IBD. Messenger is a great way to keep in touch! Dani and I met over fifteen years ago. We were representing our country’s IBD Charities at European conferences for young adults with the disease. I helped organise one of these meetings here in London in 2000 and attended others in Amsterdam and Stockholm. They were all fun, informative and rewarding meetings. I’d never been to Sweden before and absolutely loved Stockholm itself!
My ears are improving with the antibiotics now and I have been less fatigued and more productive. Today was a good day 🙂 I’m hoping my energy levels will stay raised for the next few busy days! I may have to take naps between events but I am absolutely determined to have fun and get some new photography done too.
It’s Crohn’s & Colitis awareness week and this year we’re all trying to highlight that every day with chronic illness is different. I thought that I would share my life with Crohn’s alongside something that is beautifully different! Today it’s a chrysanthemum, a favourite flower of mine to gaze upon, photograph and create artwork with.
Today I woke up feeling awful from a night of sweats, cramps and night mares. That’s usual for me though! I also woke up with another day of horrible earache. I take medication that reduces my immune system in order to treat the Crohn’s, which is an auto-immune disease. This means that I get a lot of infections but I refuse to let it deter me from getting out and about.
I set an alarm for 8.29am so I could try, for the second day in a row, to get an emergency appointment at the doctors. Yesterday was an epic fail as I slept through my alarm and by the time I contacted the doctors there were no appointments left! I tried and tried to get through today and all I got for about seven minutes or more was the busy tone. Then I fell asleep with the phone still in my hand and no appointment! That happens a lot to me as I have such bad fatigue and my nights are anything but restful.
My care assistant came to help me get up, washed, medicated and dressed at 11am and by the time we had finished and I finally got through to the doctors – no appointments! I tried pleading, telling the receptionist that I’m immune compromised and explaining my difficulties in the morning (I have lost count of the number of times I have had to repeat this conversation). She just kept telling me that I had to phone at 8.30am and everyone else was in the same boat as me. I asked her to check with my GP and she said that she’d already asked her administration manager and there was nothing they could do. I broke down in tears. An infection can get really out of control with me if I don’t get treatment quickly. I felt so stupid, it’s just earache after all! But it really hurts 😦
My hubby, Simon, called me on his lunch break (he always does, lovely man) and was utterly dismayed that I still couldn’t get an appointment. Bless him, he got straight onto the phone to the doctors and had a discussion with the receptionists about what the NHS says about their duty of care for patients who need to be seen (strong words but a calm head!). He discovered that only 13 emergency appointment had actually been available today! That’s not healthcare, it’s a lottery based on whose phone connects first. Anyway, to cut the story down just a bit, suddenly they CAN fit me in but it’s a one-off special favour?!?
I was seen by one of the doctors that I really like at 5pm who confirmed that I do have quite an infection, possibly inner and outer ear from how red and inflamed they were. So finally I have the antibiotics I need, a soothing ear spray and the relief that I will feel better soon. My hubby, my hero, thank you so much for backing me up and always being here for me!
Wordless Wednesday: Soft
Wordless Wednesday: Colour Me Purple
Happy Flower Friday everyone 🙂 Hope you all have a great weekend!