Hi
I am in another flare of dryness and I am hoping it will die down but from experience I know it is likely to take months at least. The first long flare I had lasted 5 months, the second one lasted 7 months and well who knows how long this one will last.
I am told I have sjogrens which was diagnosed via a lip biopsy. However, back to my question. I have now developed the foreign body sensation that I know a lot of you do have and for me it is a new symptom. The last flare was one of a supreme dryness and the first one was dryness and horrible eye pain. But somehow I found them a bit easier in the end(maybe they just dampened down or I got used to it) but I was wondering if when other folk have a flare, does it keep to that one sensation or does it change? My theory is that the eyes are not dry all over and the dry spots are causing the grit feeling whereas before they appeared to be dry all over. And what sensations do people find more unpleasant? I know that some people do have whatever symptoms all the time and I am wondering if that is now going to happen to me?
If anybody has any coping mechanisms, I would be very gratefull as this is driving me up the wall!
There are so many depressing stories about sjogrens eyes and I have had some probs coping with that outlook as although I am trying to accept my lot, I have not very on top of things at the present moment. I am doing lots to attempt to help this. Sparingly using unpreserved eyedrops as they only help for a few moments, cyclosporin eye ointment for 2 years at night. Moisture chamber specs and I have always worn wrap around sun glasses since my first attack in 2007. Pilocarpine started again last week. Have humidifiers.
Another poster did kindly reply to my other post (had to reregister as probs my end) and he did say that his got better but I am also anxious to know how others fare with sensations as it may hopefully give me some encouragement(greatly needed, struggling now). I have other symptoms which I pretty much cope with as obviously no choice but certain things do help them unlike this.
I have one lower plug and one lower scarring due to plug problem. About to have lower plug cauterised.
Sorry about long post. Any help very much appreciated.
Lulu
I am in another flare of dryness and I am hoping it will die down but from experience I know it is likely to take months at least. The first long flare I had lasted 5 months, the second one lasted 7 months and well who knows how long this one will last.
I am told I have sjogrens which was diagnosed via a lip biopsy. However, back to my question. I have now developed the foreign body sensation that I know a lot of you do have and for me it is a new symptom. The last flare was one of a supreme dryness and the first one was dryness and horrible eye pain. But somehow I found them a bit easier in the end(maybe they just dampened down or I got used to it) but I was wondering if when other folk have a flare, does it keep to that one sensation or does it change? My theory is that the eyes are not dry all over and the dry spots are causing the grit feeling whereas before they appeared to be dry all over. And what sensations do people find more unpleasant? I know that some people do have whatever symptoms all the time and I am wondering if that is now going to happen to me?
If anybody has any coping mechanisms, I would be very gratefull as this is driving me up the wall!
There are so many depressing stories about sjogrens eyes and I have had some probs coping with that outlook as although I am trying to accept my lot, I have not very on top of things at the present moment. I am doing lots to attempt to help this. Sparingly using unpreserved eyedrops as they only help for a few moments, cyclosporin eye ointment for 2 years at night. Moisture chamber specs and I have always worn wrap around sun glasses since my first attack in 2007. Pilocarpine started again last week. Have humidifiers.
Another poster did kindly reply to my other post (had to reregister as probs my end) and he did say that his got better but I am also anxious to know how others fare with sensations as it may hopefully give me some encouragement(greatly needed, struggling now). I have other symptoms which I pretty much cope with as obviously no choice but certain things do help them unlike this.
I have one lower plug and one lower scarring due to plug problem. About to have lower plug cauterised.
Sorry about long post. Any help very much appreciated.
Lulu
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