Hi everyone

reading your news and thoughts on MS is very helpful , thank you

I am a full time carer to my husband who has COPD and is very breathless and unable to do very much , i was diagnosed in July 2011

with MS i have already found that there is no support from the medical side and the GP can only sign post to where he thinks might be able to help rather then committing to saying YES it is the MS

Does anyone else find this?