Sorry its a bit lengthy but anyone any ideas or anyone have anything similar to the following:
Last winter 09/10 I suffered quite badly from very cold hands, never experienced this before as generally I tolerate the cold very well. However on this occasion it really meant that even taking food out of the freezer would cause great pain which would last for 20 mins or so, walking the dogs was an issue etc I also had areas of numbness in my fingers but increased sensitivity too, bizarre.
Anyway it went on for a while so I went to the Docs who firstly discounted Raynauds and took some blood tests. I went back a week later after I was phoned to come in and have a chat about the results. Seems a Professor at the Hospital reviewed the results as it showed markers for SLE (Lupus) but on evaluation it was considered that this was a throw up of my Colitis and not Lupus! I saw my GI some weeks later and as the symptoms had settled down he was in agreement with this.
However, a few weeks ago, winter 10/11 just as we have gone into milder weather than the previous month i have again started have some numbness in my fingers but also a great deal of pain if I catch my hand on something or rotate/stretch it quickly, the same for my feet and I have a great deal of jabbing pains and aches going on, worse than the previous year but similar enough to make me think i'll get the same response from the Docs and that its down to my colitis.
I should say that over the years my colitis has caused me a number of the so called extra intestinal manifestations, so this may well be the case, although its doesn't seem documented on any info I can get.
Anyone experience anything similar, worth another visit to the Docs, anyone any thoughts?
cheers
Last winter 09/10 I suffered quite badly from very cold hands, never experienced this before as generally I tolerate the cold very well. However on this occasion it really meant that even taking food out of the freezer would cause great pain which would last for 20 mins or so, walking the dogs was an issue etc I also had areas of numbness in my fingers but increased sensitivity too, bizarre.
Anyway it went on for a while so I went to the Docs who firstly discounted Raynauds and took some blood tests. I went back a week later after I was phoned to come in and have a chat about the results. Seems a Professor at the Hospital reviewed the results as it showed markers for SLE (Lupus) but on evaluation it was considered that this was a throw up of my Colitis and not Lupus! I saw my GI some weeks later and as the symptoms had settled down he was in agreement with this.
However, a few weeks ago, winter 10/11 just as we have gone into milder weather than the previous month i have again started have some numbness in my fingers but also a great deal of pain if I catch my hand on something or rotate/stretch it quickly, the same for my feet and I have a great deal of jabbing pains and aches going on, worse than the previous year but similar enough to make me think i'll get the same response from the Docs and that its down to my colitis.
I should say that over the years my colitis has caused me a number of the so called extra intestinal manifestations, so this may well be the case, although its doesn't seem documented on any info I can get.
Anyone experience anything similar, worth another visit to the Docs, anyone any thoughts?
cheers