USA Trip For Lyme Disease Treatment | third week of treatment

It’s Karen posting here (Sophia’s mum) as she is still recovering from the treatment and the journey home. Sophia’s fourth vlog shows her third week at the USA clinic when her treatment stepped up to 5 days a week, causing a lot of herxheimer (herx) symptoms – and her dad arrived to give us some support.

We really hope you enjoy watching :)

Sophia’s Fundraising Page: https://www.gofundme.com/sophiafightslyme

1 Comment

  1. Jon January 3, 2017 / 6:00 am

    Awww, reading all your struggles really bought a tear to my eye, you look so young and fragile, must be so horrible for you. I am searching for help on my symptoms which are very similar to Lyme and POTS, which lead me to your blog. I haven’t been well for close to 20 years now and sadly never had a diagnosis, I can completely understand your frustration with the healthcare diagnosis system. I was surprised how small a world it is, as I notice on one of the posts it said about you going to Falmouth, I lived there for the first 20 years of my life, I moved away 18 years ago and quite miss the place. I really hope you get the treatment you need so that you can feel a lot better or even be cured. Take care and I am sending you all my best wishes.

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