The ECHO took place in a brand new part of the hospital and was cool and air conditioned. The opthamology review took place in the old hospital and WAS NOT cool and air conditioned. It was so hot and claustrophobic, it was the closest my imagination could come to conjuring images of hell. Migraine!!
**Note: Miya's ECHO was normal and (insert trumpet fanfare) her corneas are only lightly clouded. Her iris colour can be seen through the light, and her eyes are hazel!!
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The onslaught of warm weather means that our back garden has suddenly become home to a paddling pool. Despite the hosepipe ban, we have been permitted by our water company to fill the pool with buckets. About 40 of them. And it's not even full. Miya has had a blast in it but putting sun cream on her remaining hairy body parts is a NIGHTMARE!!
She's got a hairy back!! |
Miya has started speaking in short sentences which usually revolve around cats, shoes, and doors. She has also started saying "Daddy" as opposed to "Dada". She has starting whining and having small tantrums (typical of a nearly two year old). She makes me laugh and she makes me shout and sometimes, I feel like I might have a nervous breakdown.
She did this to herself |
At the cafeteria at Great Ormond Street Hospital |
I was recently contacted by another mum of a Hurler's baby. She reads this blog!!! I was amazed that someone other than my father reads this blog!!! We're meeting up on Tuesday!! I love meeting other MPS families because they know what I'm talking about when I mention "enzymes" and "GAGs". They don't think I'm long-winded when I talk about MPS and they understand Miya's unique appearance. (Although a frined of mine told me the other day that Miya's unique look makes her very pretty. Awww shucks!!)
I'm unimaginably tired. Miya is busy, therefore I am busy. There aren't enough hours in the day and by the time Miya goes to bed, I just want to sit and stare out the window and vegetate.
As a family, we are looking forward to the summer time and I am planning on taking Miya to Peppa Pig World for her birthday (Chirs has been notified of this plan. I'm assuming he's coming along too).
It was great talking to you & can't wait to meet you all xxx
ReplyDeleteJust to let you know there are more people reading your blog... My name is Sandi and I live in Australia. I have a daughter with Hurler Scheie who is 5 years old.
ReplyDeleteThanks for reading, Sandi!! I've read your blog, too! How is your daughter?
DeleteIm reading your blog too! Our daughter Chloe was just diagnosed with hurler's and we are just starting treatment at GOSH.. It would be great to meet you... Thanks for blogging we need all the info we can get...
ReplyDeleteMy email: teresa.alvarez.pino@gmail.com
Hi Teresa! I've sent you an email. Thanks for reading!!
Deletehello! My name is Katrina, and I am a sophomore in high school. I am currently doing a project about Hurler's Syndrome, and was wondering if I could interview you for a couple of questions that I have about this disease. It would be great if you could email me back at my email: katrinamarirufin16@mittymonarch.com
ReplyDeleteplease respond as soon as possible... thanks :)
Hello Sarah!
ReplyDeleteMy daughter is currently being diagnosed for Hurlers... is there any way I can contact you? Your blog has been a consistent source of hope for me.