| About Sensitive Foodies |
Nowadays, for a variety of health or lifestyle reasons, more and more people are making the decision to eliminate certain foods from their daily diets. Unfortunately, doing so is easier said than done. An incredible amount of time can be spent trawling through recipes books, reading the tiny print on ingredients labels, quizzing shop assistants and waiting staff, and finding places that serve suitable meals. That is what we found when starting to follow the Best Bet Diet (FAQs). We would like to ease the process of eating well on a restricted diet, and that’s why the idea for Sensitive Foodies was born in 2007. Our aim is to make following a restricted diet easier and more enjoyable, and to enable others like us to share and exchange information about food and eating experiences at home, out, or abroad. We were lucky enough to catch the eye of UnLtd, a charity supporting social entrepreneurs; they awarded us the funding we needed to get the site up and running in 2008, and eventually launch in February 2009. Who are we?Kathy KohlKathy's story ![]() In 1985, when I was a feisty young student of 20, I woke up with what appeared to be a stroke: the right side of my body was almost completely paralysed, and even my mouth was lop-sided. I was soon diagnosed with Multiple Sclerosis (MS) and given steroids, told that there’d be no more late-night partying for me, also that I should lose a bit of weight and that unfortunately there was no ‘magic cure’ for MS... For the first ten years, I suppose I was ‘in denial’. I didn’t tell people about the MS unless I had to, and apart from going to the gym, taking Evening Primrose Oil and giving up red meat, I didn’t focus much on what part I could play in managing my own health. However, despite intermittent relapses, I lived life to the full, spending most of those years living and working in Portugal.
Pics: Dinner at Lisa's in 2010, yum! Abseiling to raise funds for Sussex MSTC, summer 2008, yikes! Lisa FinchLisa's story When I first had optic neuritis (inflammation of the optic nerve leading to temporary loss of sight) in 1998 the hospital didn’t tell me it can be early symptoms of MS, and offered me no support with dealing with the condition. You can imagine the shock I had when I went on line and did my own research. It was at this point I decided I had to find how to manage my health to avoid my condition getting any worse. ![]() Thanks to Kathy, I discovered the MS Treatment Centre in Southwick where I go for High Dosage Oxygen Treatment, pilates, shiatsu and support. It’s a fantastic centre with all sorts of therapies to help you maintain a healthy life . What is more, the therapies are subsidised making it affordable so you can have regular treatments. Contact them at www.mssussex.com. There are MS Treatment/Therapy centres across the country if you want to find out more, go to www.msrc.co.uk. In June 2006 I decided to try the Best Bet Diet (or Palaeolithic Diet) after meeting several people who had tried it out and strongly recommended it. I can certainly feel the benefits and the more I research, the more sense it makes; it has also made me aware of how many other people have food intolerances and could benefit from the information Kathy and I have gathered. Don’t worry so much about what you can’t eat, it’s just a change in habits and lots of fresh food and chopping. The hardest time for me is eating away from home and being tempted by homemade cooking at friends’ houses that might contain wheat or dairy. Most restaurants that serve good healthy food will have something for you on the menu and most chefs are happy to adapt dishes where possible. Look out for features on our homepage about other people’s experiences and go to the numerous links to find out all you need. Photo: Lisa unwrapping some fragrant and delicious Thai-style baked fish, January 2010. Watch out Masterchef! |