I totally sympathaise with you Carrottop and like many others I am also a 24/7 carer for my DH. Thankfully most of the time I am fit and healthy but after tripping over a few years ago, I now suffer from Trigeminal Neuralgia, named after the nerves in the face, which was damaged from the fall. The pain is like toothache but ten times worst. It is rare , associated with patints with MS. As no training has been given, doctors think its a migraine; which it is not, nor it is a headache . Anyway the journey to the diagnoses was long, two years of frustration, with just about everyone in the NHS dimissing my plight. Cutting long painful story short I eventually had a MRI scan and a letter from the Consultant confirmed this condition.
This condition can be triggered by anything from a sneeze to a puff of wind. My last attack was so bad I went to GP, with my letter, but was yet again dismissed with a migraine. After two days of total disability, my sick DH took me to A&E. Had the usual wait and was told to come back the next day to the ambulatory unit, There I had the usual checks, and thankful I remembered to give the doctor my letter. She phoned the consultant, who confirmd the problem and prescribe the pills. There is no official medicine for this condition but these pills worked. To this day there has been no follow up and like my husband we are left to get on with it.
This experience did leave me scarred, vunerable and worried about what would happen to my husband if I went first. However, one postive thing that came out of this was that my husband also realised what I , as his carer , do for him and he is now more appreciative of our situation because if I am imcapactiy he has no one.
We also realised the NHS is good for emergencies anything else, take a pill.
What do you think about my situation?
Hair loss ....anyone with any advice please?




