hello all hope you are feeling ok. This past week i seen a neuro who has diagnosed me with fnd (functional neuro disorder) non psychiatric so fully software malfunctions as mri was clean as was ct:)....
well i am now at week 3 of my migraine with one of those weeks being spent in a hospital. hospital put me on 900 of aspirin 3x a day , 1000 paracetamol, 100 tramadol 4 x a day plus 40 of omeprazol,...
My doctor (gp) said i had fybro 'probably' sent me to a rhumy and she said nope its hyper mobility syndrome ( took under 5 mins of bend this way that way and how dose it hurt questions), i have a...
hms = hyper mobility syndrome :) (altho i do have ad with my dyslexia), yeh iv had all sorts for migraines and after 2yrs i am finally referred to a migraine clinic with a huge waiting list......
nothign they gave me nortriptaline and diclofenac :/ i cant take codien so they said thats it....
SO i was told i had hms, ibs and asthma and then to top it all of i get migraines that end me frequently in a&e. Recently iv been flat out tired sleeping till 2pm in the day or not sleeping at all...
yes im to try get a bracelet or something, but as i have lots of allergy too it wont all go on a thing like that so for the now i have a bit paper referring them to a usb stick with my info...
thanks for the replys, im laste in back to this as on friday eventing i was spotted by another student livign in the building and she was shocked by my lack of speech and called fron 24 hr services...
i have recently moved to student accommodation, i have a history of sever acute migraines that can effect speech and orientation along with sickness and other symptoms. The new place im in seems to...
SO i seen my rhumatologist at the end of april, and after less than 15 mins she decided i have Hypermobility syndrome. She did a bunch of other blood tests but as per my body lol they all came back...
Thera im in scotland i dont actualy pay my docs unless i go private, meaning my doctor gp is not really firable and i have changed my gp which was akward since i cant change surgery as there is only...
so on I go .. new doctor more test a year on still nothing :( No diagnosis but at least shes looking I guess last docs refused to diagnose just kept telling me I was diagnosable :/. So I have now...
Its review week.. woot lol. Im up to 100 mg topimax and no migranes and reduced body pain it apears that my docs experament is somewhat working? Downside is this may help lead down fibro/cf path......
on sat I did some xmas kiddie shopping with my gran :) was fun but was back in bed as soon as foot in door as all wandering about for hrs did me in , Sunday It rained and I was still sore but I was...
stickie?...
oh noes I mean it steps up every 2 weeks not entirely over to weeks eep that would be a disaster! tho today im still in pain and ibs decided it wanted to join the party so bed day it is :/ , doc said...
Sometimes im glad I live in a nanny Scotland 'state' where we got weird drug controls and stupid laws over contols over what and who gets what( not inc cancer paitents I feel bad for them as south...
so I was put on this 'topiramate experiment' but doctor upon doing so said only paracetamol! but i get cute migraines the type that cause week long hospital admissions... iv had a migrane for over a...
I personaly dont know, but given iv had migranes since i was 12 and had both ct, mri and fmri all show clear no abnormalitys or leasions etc. Id be tempted to say *imo* that possibly not, but good...
Thank you for the responces, i seen the doc today that seems to know things. He has put me on topimax again till i get to 100 to see if it will help. No referal untill after my my "topimax...
im new here but I thought id post for some advice, ill explain my situation first.So for past year iv undergone a spectrum of tests starting last oct with 6 lumbar punctures that only showed a...