G.I.F.T: Do you write poems?

G.I.F.T: Do you write poems?: Hi everyone! After receiving great feedback on facebook about poems, I thought it would be a great idea to get everyone to send in their ...

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What to do if you think you have Gastroparesis #Part 2

Please click here for  #Part 1 So, you went to your GP and the chances are... you came home with a bunch of pills and were told to go back if things didn't improve. This is standard practise and you mustn't feel that this is a brush off in any way. There are several medications that help improve gut motility and nausea so it's highly likely that you will try a few before you find a regime that suits you. Remember: When they say come back.... they mean it. Doctors don't chase their patients and if they don't see you they will presume you are ok. It is best to give any medication a good chance to get into your system so don't expect immediate results. 4 weeks is usually enough time to know if something is working for you or not but some medications can take longer than this. In that time, there are many things that you can do for yourself to help minimise your symptoms. Dietary changes are a must when it comes to gastroparesis, no matter how hard ...
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Gastroparesis, EDS & the Final Piece of the Jigsaw Part #3 / Cranio-cervical Instability!

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I know I left Part 2 somewhat in the middle of the consultation, so I'll try and start where I left off and see where it goes. Obviously there are inevitably going to be more "parts" to this series the deeper we go, so bear with me I WILL get it all down on here eventually. To sum up the last post in a few words, the diagnostic term for my neck issues is, Cranio-Cervical Instability. Naturally our next question was, "What can we do about it and what does it mean for the future?" This is where I struggle to explain. When it comes to brain/spinal surgery the decision process is not so cut and dry! So, the only way to actually fix the instability in my head and neck and prevent any further neurological damage would be to fuse my skull and top two vertebrae together using metal rods (permanently immobilising my skull C1 & C2) and remove the excess tissue that is causing the brainstem compression. Obviously this is a very risky procedure and not one...
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Please help me to create a useful resource for people who suffer from functional gastrointestinal disorders. Your comments would be most valued. I would like to hear from anyone who suffers with pain after eating, unexplained vomiting, irritable bowel syndrome or general stomach pain on a regular basis. I would also like to hear from people who are unable to eat for medical reasons and are either living off supplements or fed through a tube (PEG). It would be great to hear your stories and how you cope. After 10 months of pain I finally have an answer! I have now been formally diagnosed with Ehlers-Danlos Syndrome and would love to hear from other people with this condition. xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx Please post any comments or suggestions you have below. Unfortunately I can't enable comments on individual pages, I'm still learning lol. 19 October 2010 10:47 
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