Double trouble! 

Gosh, I defiantly have a lot to catch up on since my last post. I apologise for the long writing break, it’s been a very busy couple of months as I’ll soon explain. But firstly the main event AMERICA AND THE PDSA! 

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Life still goes up!

Wow! 4 months have flown by since my last post, and so much has already changed in my personal life. I was not  expecting so much to change in such a short space of time. But every change has been for the better. I’m currently in a new relationship which is very exciting, and all aspects of my life really seem to be falling into place. This time last year was the beginning of my remission, I was still very worried and concerned that my luck would change and my counts would drop, I felt like the worry and anxiety of a relapse would haunt me for the rest of my life. I could not have been more wrong. Continue reading

Merry Christmas!

Merry Christmas and Happy New Year!

I’m not even sure where to start. Reading through my previous post I feel like the worry and anxiety was a lifetime ago!

When my appointment came round I was very eager to talk Dr Whittle about my little episode. However, with high stable counts again their really does seem like nothing to worry about at the moment. That said, I don’t have another appointment for 12 months!!! Now that is Remission! It’s so difficult to get my head around but I am over the moon. As long as I don’t have any reoccurring symptoms, I should be hospital free. (Also providing I don’t have a clumsy episode that lands me in Accident and Emergency, fingers crossed-ey!?) Continue reading

APS Scare!

After my bizarre episode, one of my first ports of call, was the PDSA forum. Everyone there is so helpful, and most, like Sandi, have seen it all. I felt bad posting after leaving it so long without popping by. Sandi and a few other suggested getting checked out for something called APS. APS is a auto immune disorder linked with ITP, where your antibodies basically cause blood clots and TIA’s (mini-strokes). They were concerned that the migraine may have been a TIA, or a warning sign for APS. It can be tested with a simple blood test. I tried my hardest not to panic, but I’d be lying if I said didn’t.

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I wasn’t expecting that…

On Monday 23rd October, something very strange happened. I was driving back from work when I started to lose the feeling in my right hand and the right hand side of my face. I have terrible circulation and its getting pretty cold now, so I didn’t think much more of it. Although when i got home, I was finding it really difficult to speak, I knew exactly what I wanted to say, but every time I opened my mouth, it was like I was speaking a alien language. No matter how hard I tried, the words and letters were all muddled up. I started to feel really uneasy and strange, so when my speech returned to normal I booked myself into the doctors, I figured it might be something to do with my thyroid again.  Continue reading

The Mission Platelet

HAPPY ITP AWARENESS MONTH EVERYONE!

Today I attended my second ITP convention in Bedfordshire. The Support Association was celebrating their 20th Anniversary since the foundation was founded, alongside the Grand opening of the new Headquarters to be known as ‘The Platelet Mission’. Midsomer Murder star Neil Dudgeon cut the purple ribbon that hung from the door, alongside a great speech recognising great things to come. Unlike like the last convention, we had guests that had travelled all the way from the Netherlands to celebrate the opening of the new headquarters. A special thanks was given to the ‘Cavaliers’ whom had raised over £33,000 for the Association after losing a fellow family member with ITP to a severe head injury. In recognition of the money raised and the loss of  23 year old Steven, a room was named the Steven Sim’s room.

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