Still on that boat…

Strawberry blonde in a dizzy world!

More quality time…

February7

…with the floor. It has been such a bad few weeks. I had a trial escape but I managed to have a ‘Power Down’ so it wasn’t that successful. I was going really wild having a cup of tea at my Aunts. I mean who manages to pass out in a chair?!?! Me evidently. After being carried to the sofa, where I remained for a couple of hours as I couldn’t move, I decided leaving the house isn’t really an option. Laying face down on someone else’s sofa for what felt like an eternity was a pretty big clue! I mean a gal just wants be on her own floor if she’s gotta be on a floor right?

It has become so normal now that when my Mum comes to my house and it’s quiet she presumes I’m on the floor somewhere and has a good look around. Problem is if I can’t leave my house how am I going to leave the country for Washington? Only time will tell.

No picture. I am fed up. All creativity has been sucked out of me, oh here you go this will have to do 🙁

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Who am I?

Was – independent, intelligent (with plenty of dizzy moments), successful, busy, funny (depending on how much Prosecco I and the people around me had!), quite stressed out but overall happy, without even realising how lucky I was.

Now  – ? just a mess really! I was diagnosed with Migraine Associated Vertigo (MAV) two and a half years ago when my life changed dramatically. It’s a variant of migraine that means I feel dizzy and tired nearly all of the time. If I try and do anything ‘normal’ this sparks of vertigo which gradually gets worse and worse until I pass out unless I lie down for hours, sometimes days. What this means is I spend 90% of my time in bed in a quiet dark room. Normal activities like shopping, walking, going anywhere bright or busy, the cinema even visiting friends who have patterned wallpaper or a gravel drive is a nightmare!

I’m continually trying new medications, all of them with quite nasty side effects (worsening of vertigo, weight loss, hair loss and sense of humour loss to name but a few) to try and find the magic one that will work for me. Fingers crossed the one I’m on now will work, time will tell.

A good friend set up this website so I could become a ginger whinger. No I’m kidding, so people can understand what I’m going through and maybe it would help me to have a bit of a rant. I have quite a dark sense of humour, I think that’s the only reason I haven’t gone completely bonkers! I clearly don’t have the most exciting of lives but I live in a small village with some entertaining characters and I’m always having blond moments (I blame the meds but I’ve always been a bit dappy!). Who knows I may even get better, and I can assure you life will be filled with amazing adventures then!

Scrap that! After zillions of Consultants all saying that they know what’s wrong with me and that they can get me better. Endless drugs and procedures I was finally Diagnosed with Chronic Lyme which was great – until I find out that nobody in the UK has a clue how to treat it. That complicates things some what 😉

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