The resurrection of breakfast

It had always bBreakfast Smoothieeen drilled into me that “Breakfast was the most important meal of the day” but I had always ignored it in favour for that one last snooze or two in bed, and quite frankly I’m never that hungry in the morning.

After my diagnosis with CFS, I went to a nutritionist who helped me figure out the best foods to eat to try to relieve some of my fatigue, it was during this process I found out I had a gluten intolerance.

I worked with my nutritionist to come up with something that worked for me, as breakfast became even more important with my diagnosis. Continue reading

Starting down the Gluten free (GF) path

Starting down the Gluten free (GF) path

When my nutritionist told me I had to go gluten free, I genuinely wanted to cry.

I thought that my baking and days of eating out were over, I love all things full of gluten goodness from pizza, pasta, bread as well as cakey things and I felt like it would have to cut out everything I loved out of my diet.

Luckily this was not the case, three things really helped me get on the right path. Continue reading

Review: Waitrose LOVE life gluten free millionaire blondies

Waitrose BlondieI brought this product assuming it was just millionaire shortbread, which at a glance it looks like.

Turns out these actually have a blondie base (white chocolate brownie), these are pretty sickly one is defiantly enough to satisfy any sweet craving you might be having. Continue reading

Getting Diagnosed CFS

In the beginning
In the fall of 2013 I started to experience a variety of symptoms that included extreme fatigue (worsening 24/48 hours of activity), headaches, muscle ache & weakness as well intermittent dizziness.

It really stopped me in my tracks. I went from being able to juggle work, studying for my ICAEW exams, Chairing a local charity as well as having a very active social life; to being house bound (sometimes even bed bound), I felt like everything I had worked so hard to build was slowly slipping through my fingers.

My work &  GP were great really supportive, I initially got signed off for a few weeks whilst we tried to figure out what was wrong, work straight away put me on a phased return (3 days a week & reduced hours) as well as getting an external vocational rehabilitation adviser involved.

This however was still too much I was calling in sick on a regular basis, getting frustrated at myself for not getting better or understanding what was going on. The GP ordered endless blood tests, all of which continually came back negative.

Getting Diagnosed
As things worsened my GP explained to me that she thought that I had CFS/ ME, but I needed to have yet more blood tests done as a process of elimination before she could make the diagnosis and refer me onto a specialised clinic.

Once these came back negative at the end of Jan 14, she made her diagnosis and I made the decision to get signed of work at the recommendation of my GP (something that I resisted up to this point). She wanted to sign me off initially for 3 months, but I was very taken back by this so compromised at 1 month, as at that point I was not psychologically ready take so much time off (I later got signed off for a further 2 months, taking my time off to around 3 1/2 months).

I was referred to the South West ME/CFS Clinic held in Frenchay Hospital, I got my referral through in March, but had to wait until June 14 to get my first appointment.

Having a supportive and understanding GP is essential, if you don’t my advise to you is keep switching until you find one that understands what you are going through.

I found the NHS website pretty useful in letting me know a bit more about the condition and what I should expect.