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My Journey with CFS

Nutrition. Love. Healing.

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Alot of people ask me what I take to treat my Chronic Fatigue/Lyme Disease so I thought I would do a quick blog post on what I do currently to heal my body:

  • I've been doing the Cowden Support Programme from Nutramedix for over two years now and its made an incredible different to my health and all my symptoms.
  • Nutrition (obviously) - I eat a clean varied diet of organic whole foods, fruits and veggies, home made meals, mostly gluten free & dairy free (& lots of herbal tea)

    • I take basic supplements for optimum health & mitochondria support (for energy production)
    • Medication for an under active thyroid after multiple tests
    • I sleep on a grounding sheet and keep my exposure to wifi and electromagnetic stress to a minimum. I also try to be in contact with the earth as much as I can (bare foot) Why grounding?

    • I try to use natural body products as much as I can (exfoliate with salt, lemon juice & olive oil, remove my make up with coconut oil) - most products contain nasties which we absorb and struggle to detox, clogging up our system. Check your make up, shampoos and products for parabens, phthalates and sodium lauryl sulphate.

    • I keep my environmental toxins to a minimum - be aware of mould exposure and the dangers of it, paint, household cleaners, perfumes, tap water, pesticides on foods (eat organic) - again producing toxins our bodies are not made to detox
    • I did Cognitive Behavioural Therapy (CBT) for 2 years so I am very aware of 'how to think' basically thinking positively, being gentle with myself (thats a challenge), taking time to relax, being aware of toxic thoughts

    • Pacing - knowing how much I can and cannot do physically and mentally
    • The Perrin Technique - I've been doing this for 6 years. It is designed for CFS patients and it is draining the lymphatic system of all the toxins in our system.
    • Pray and trust in God - it gives me peace and a trust that God has got it all covered and he's in control

    August 2014

    OK that was meant to be short, it seems like alot but thats life with CFS/Lyme. I see it is a lifestyle change in order to be well.
    It's different for everyone but some of the above are so important if we are looking forward to a healthy future.

    Lots of love xoxo
















    It's that time again... You know... Relapse time? I hate relapse time it's so less than ideal.


    Relapse time is like the most surreal of times, like someone has come in and in one swoop taken everything you enjoy away and your like "Wow what happened there?" - you know what I mean.

    It's so annoying because there were no signs, I live by signs and there was nothing!! I felt so well, which makes it even more frustrating!

    I'm pretty much house bound, just in bed and the sofa. Thank goodness for Joe's Netflix account and these two Cockapoos. The severe fatigue, the aching, the weakness, the emotions, the brain fog, the loss of appetite, the frustrations.


    Don't get me wrong I know i am very lucky, alot live in total relapse and i'm moaning about 2+ weeks. It's so typical CFS/Lyme, who knows when it will strike and we live not knowing how long it will last for. I can't get too frustrated because it only makes things 10x worse.

    Lets just wait it out and see what happens I guess.
    It's given me alot of time for reflection, not sure on my conclusions on life... I will get back to you.
    I do know I have an amazing boyfriend, family, friends, church family & work - so I am very thankful.




    Have a healthy week
    xoxo




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    About Me

    About Me

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    Hi my name is Becky. I have a great love for health & nutrition, currently finishing my Nutrition diploma with CNM & cuddling lots of Cockapoos.

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    My Journey with CFS

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