Later today the phone line will be disconnected and my year in France will be nearly at an end. So this is my last post from France.
There will be more posts on the blog to come when I return to the UK. I want to sum up the year and also fill in a few of the gaps - thoughts I have jotted down in notebooks and on my computer, but never got round to posting here.
I have a busy two days of packing and cleaning, but I feel that I've ended my year on a good note and I am ready to return to the UK.
On Tuesday evening we were taken out for dinner by a French couple who have become good friends. Although I have been plagued by wildly ambivalent feelings about our return, during the meal I thought "I really don't want to go back" and I suddenly felt very much at ease and ready to return.
I guess one of the feelings that had plagued me was a nagging doubt that I wasn't entirely comfortable in France. On Tuesday night that doubt evaporated.
I felt that I would be okay if I didn't go back to the UK - that I could live in either place. I'm not sure I can explain these feelings any more, but it has given me a real sense of peace.
One final thing I want to clear up before I log off is about the NHS and health care in Europe. I've noticed that a few people in the USA have found this blog via a web search - perhaps in response to the huge debates around health care in their country at the moment.
I am critical of some things about the NHS and have found the French system to be better is some ways. However, I do love the NHS very dearly - as do 99.9% of the British population.
My criticisms of some aspects of the NHS and my involvement with Crohn's and Colitis patient organisations and health care pressure groups in the UK are to make the NHS better - and to keep private health care out of the NHS.
My main grumble is that there is too much emphasis on budgets, internal markets and cost-efficiency in the NHS. I believe health care only works for everyone as a public service not as a business.
Having read accounts from young, middle or working class americans getting ill with Crohn's disease, I know I would probably have died or bankrupted my parents - or both - if I had grown up across the Atlantic.
If I was a US citizen and I had survived, I would be knocking on doors 24/7 arguing for health care reform.
There - I hope that is clear.
Au revoir!
Friday, 14 August 2009
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3 comments:
Hey I am a student coming from the US to france and I have Crohn's too. I was wondering where you had your treatments and how you found out which hospitals offer remicade. I am going to be staying in Pau and I will need to receive treatment while I am there. Any tips would be a big help.
Hi Nicole. That's really exciting! The best thing is to check with the French Crohn's & Colitis association - AFA - (link on the blog) and also look up the website of the local university hospital and contact one of the doctors in "Hépato-Gastro-Entérologie". I am sure they will offer remicade and all the other anti-tnf drugs. These are far more common in France than the UK.
Probably best to contact the Crohn's & Colitis Foundation of America and they might help with advice on insurance etc. Your university could help with that too.
Your insurer should tell you what you need to do to 'get into the system' - I think you'll be part of the French national health system, just paying for it differently?
You definitely need a letter from your doctor in the US, giving a summary of your medical history - and get it translated into French!
Most of the hospital doctors do speak good English, but you never know...
It will be a little worrying and stressful getting it all sorted out, but your experience of France will be far richer from your occasional trips to hospital for the remicade. Definitely learn some relevant vocabulary - it's all the French I can remember...
Good luck!
Andy
Why isn't mainstream using Trichimonas suis as found to cure Crohn's by the Universitu of Iowa years ago. Helminths
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