Do you know the month your parents and grandparents were born? If you do, please help with this RESEARCH SURVEY. There is an incredible amount of info on MS out there on the internet. It’s daunting to know where to start. ‘Little Black Book’ takes you straight to the most relevant pages available. Navigate links by topics from the ‘tag cloud’ at the top of the page. The Shift.ms community is for everyone on the internet, but content has a UK bias.
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Vision Money MS info Education Getting about Holidays Work Family Complementary Diet Exercise News Community Research Relationships Equipment Support Blogs LinksWhen should I tell someone I am dating that I have MS? I think this situation is really common. I happen to be one of those people who are pretty open about their MS status, especially since I started writing on the topic (actually, I probably tell far more people far more information much sooner than I need to........   The Face of MS: A Boyfriend's Perspective There are many faces of MS. Not just the persons who are diagnosed with multiple sclerosis, but those around us who share in this experience. Dating when you have MS can present special challenges. I’ve invited Rob to share his perspective and experience with us today, to discuss how MS has affected our lives and our relationship. Please welcome Rob to the community. I'm not drunk, I've got MS My name is Emily. I have MS. I don't think this should change who I am. I really hope it helps others with MS (mystery s as i like to call it!)see that life does go on! Please have a read and let me know what you think! Me, My MS and I Jenna Anderson's blog on living with MS and staying positive. Great info for the newly diagnosed and more experienced MSers alike - "Life is still fab with MS" When Should I Get a Cane if I have MS? Maybe immediately, maybe never. Like everything else surrounding MS, this is a question that is highly individual (and may change on different days or when we are in different moods).Source About.com Multiple Sclerosis 20/10/09 Living day to day with multiplesclerosis My name is Tara. I have been married for 16 years. We have 3 children. I was diagnosed with Multiple sclerosis a little over 2 years ago ..... Complementary and Alternative Medicine and MS This is an American site but nevertheless gives some quite sensible advice on various CAMS. There is a brief explanation of each therapy, with a link to learn more details Skill - National Bureau for students with disabilities We are a UK independent charity that promotes opportunities for people in learning and entry to employment. Since 1974 we have been helping young people and adults over 16 years of age with any kind of impairment including physical and sensory disabilities. MS Society guide to benefits Highly deatailed information from the MS Society about the range of benefits that may be available to you if you have MS MS Trust Guide to Benefits Information on claiming benefits and tax credits for people with multiple sclerosis. From the MS Trust's Living with MS pages. MS and Insurance The MS society provide useful and specific information on this topic including links to specialist insurance brokers Living with low vision NHS resource on low vision and low vision clinics.Nearly 2 million people in the UK are affected by low vision, but you can maximise poor eyesight if it's dealt with properly Low Vision Aids An American website providing comprehensive resource on low vision tec from magnifiers to CCRV's as well as computer and internet access technology RNIB RNIB work to enable people with sight problems to live their daily lives independently.Call our Helpline on 0303 123 9999 for information about sight loss and how RNIB can help you. This sevtion of the site deals with access technology MSRC section on vision & MS An overview of some of the common visual disturbances that can occur in MS. There is a link to the seperate section on thwe most common of these, optic neuritis Wheelchair Kamikaze I'm Marc, a 46-year-old male, living in New York City with my lovely and wonderful wife Karen. Diagnosed with Primary Progressive Multiple Sclerosis in March of 2003, I now require a wheelchair to get around the city. I like to drive the wheelchair at full speed, thus the moniker "Wheelchair Kamikaze" Exercises for MS A nice concise guide to the differet types of exercises that are well worth getting into if you have MS |
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