I would love to invite all of my followers here to subscribe to my brand new blog on http://www.serenkiremitcioglu.com. Let me know you've subscribed and I'll make sure to follow you back! I'd also love to connect on Facebook and Twitter. Find me on Twitter @serenkwriter, or pop a like on my page: https://www.facebook.com/serenkiremitciogluwriter/ Here's … Continue reading What you missed on my new website…
A Weekend In Brighton
Read my latest blog post about my weekend in Brighton, here!
#SpoonieSeren: Autoimmune Diagnoses Need A Mental Health Care Plan
Read my latest blog about autoimmune diagnoses and mental health care plans, here. Sign up to my brand new blog and never miss a post!
#SpoonieSeren: A Disability Identity Crisis
Read my latest blog about disability and identity, here.
#SpoonieSeren: Living With A Stick
🥄 Welcome to the #SpoonieSeren Series! 🥄 Being diagnosed with Vasculitis at the age of 20 in November 2017, I've been thrown into the deep end of an invisible, chronic disability. This series is going to explore my experience with disability - what vasculitis is, what it means, how I suffer from it, etc! I'll … Continue reading #SpoonieSeren: Living With A Stick
Check out my new website!
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A Personal Update
Finishing off the third year of my degree whilst working full-time has been somewhat of an undertaking - amazing, fun and empowering, but an undertaking all the same. Maintaining a social life and a healthcare regiment alongside this has meant throwing blog-writing into a box and chucking it into the loft to gather some cobwebs. … Continue reading A Personal Update
Rare Disease Day 2018: Rare and Real
According to Rare Disease Day, 'a disease or disorder is defined as rare in Europe when it affects fewer than 1 in 2000.' Searching for my disease on Orphanet, it turns out that I'm between 1/70,000 and 1/100,000. I have scored the EGPA jackpot, that's for sure! https://www.youtube.com/watch?list=PLw82lJoP71WhRRUPnNeap9eYHB7qROv1A&v=CLs5Q1XUiUg Rare Disease Day addresses the common problems faced; "The … Continue reading Rare Disease Day 2018: Rare and Real
The Scratchworks Theatre present The Snow Beast: A Review
Four incredible women made their way onto Barbican Theatre's humble stage this Saturday, gracing their family audience with a show like no other. After battling through the typical Devonshire elements, I sat down to watch The Snow Beast, a show I'd been highly anticipating for quite some time. Created by The Scratchworks Theatre Company in association … Continue reading The Scratchworks Theatre present The Snow Beast: A Review
Sigalit Landau // Barbed Hula (2001)
Winding through the tourist scattered streets of Málaga on a Sunday afternoon, sun beating down on me, I headed to El Centre de Pompidou, a smaller branch of the world famous contemporary art gallery in Paris. Making my way through the gallery, I stumbled across many striking exhibits, such as ‘Self Portraits’ which featured feminist icon Frida Kahlo’s The Frame (1938), as well as a sincerely thought provoking exhibit, ‘The Man Without A Face’. However, it was the gallery’s segment for ‘The Political Body’ that struck my attention most. This is where I discovered Sigalit Landau, an incredible Israeli female artist who uses video, sculpting, installation and her own body to create political art. Her art was astounding, but her message was even better.
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