Still on that boat…

Strawberry blonde in a dizzy world!

Day 39, 40 and 41

November29

Almost there. Had to put the last few days all in one post as that is how exciting they have been, can’t even get a flippin paragraph out of it! The Patch was far from successful, it gave me blurred vision which made the vertigo that little bit more problematic – just what I needed! I’ll write more when I can see again, this is so far from funny!

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7 Comments to

“Day 39, 40 and 41”

  1. Avatar December 10th, 2015 at 10:01 am Snowy Says:

    Fingers crossed it begins to pay off soon Sues xxx


  2. Avatar December 15th, 2015 at 5:27 pm Susan Cartwright Says:

    I so hope so!


  3. Avatar December 12th, 2015 at 8:28 pm Emma Says:

    So how are things now? Any better?


  4. Avatar December 15th, 2015 at 5:27 pm Susan Cartwright Says:

    No, I can’t tell you how disappointed I am 🙁


  5. Avatar December 16th, 2015 at 8:26 pm Emma Says:

    How long can it take to see an effect?


  6. Avatar December 17th, 2015 at 7:57 pm Susan Cartwright Says:

    I’m not seeing my specialist for a couple of weeks but speaking to his colleague yesterday I got the impression that it’s looking like it hasn’t had the effect expected/required 🙁


  7. Avatar December 18th, 2015 at 8:41 pm Emma Says:

    That’s a shame Sues, but don’t let it get you down – don’t think ‘the treatments haven’t worked’ but instead focus on ‘the treatments haven’t worked YET’. Keep the positive thinking! Enjoy the mulled wine xx


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Hi, My name is Susan and in 2010 I suddenly got very sick with vertigo and extreme fatigue. My life as I knew it changed forever. I had to leave my job as a junior Doctor to move back home with my family as I was unable to look after myself, let alone other people. It took a very long time, about 2644 doctors visits and ALL the tests to be told ‘congratulations, all your results are normal there is nothing wrong with you’, which was the most devastating news of all as there clearly WAS something horribly wrong, we just could not identify it.

 

Eventually, I was diagnosed with Chronic Lyme Disease which was great news as I finally had a reason to feel so ill. That was until I realised that there is no real recognised treatment and I was once again left to trying to navigate debilitating symptoms alone. More doctors, more tests, protocol after debilitating protocol and plenty of ‘ah ha’ moments later I finally started to heal. It was quite the journey and I have learnt a lot about what treatments are out there, and perhaps more importantly, the body’s amazing capacity to heal. I am now in a position where I want to help others to reclaim their health.

 

@still_on_that_boat