New here.....and VERY embarrased
Posted: Thu Nov 17, 2016 7:32 am
Hello all......my name is Lisa. I am 42 years old. Recently diagnosed with Sjogren's Syndrome (April 2016). I was also diagnosed with Pars Planitis in Sept of 2015. I have been having a myriad mystery symptoms this past year but something happened last night that I just can't seem to deal with.
I woke up around 3 a.m. to go to the bathroom. On the way to the bathroom I noticed that my sleep pants were wet. When I sat down to pee, I realized my panties were SOAKED!! And my sleep pants were more than just wet! So I emptied my bladder the rest of the way, cleaned myself up, put on dry bottoms and thankfully my bed was not wet! So I laid in bed for over an hour BAWLING!!!! I have been having problems with urgency & frequency lately. But waking up wet....was a first. And I hope the LAST TIME!!!
Some of my "mystery symptoms" include: clumsiness, numbness/tingling in toes & heels, "bee-like" stings on tops of feet, trouble swallowing (despite being on a saliva stimulator) and now the bladder control.
These issues don't happen everyday. I may go weeks without experiencing them. Even then I don't experience all of them.
I see my Rheumy again on 12/12 but I don't know if I should wait that long??? I am dreading going to bed tonight already!! I am already cutting off all fluids at 8 p.m. (I go to bed between 9:30 & 10) and I don't have a UTI or anything like that (just getting over bronchitis & PCP ran blood work and no sign of infection in blood work) and no other signs of infection noted.
So.....what I am getting at is.....since I already have an autoimmune disorder, and I have Pars Planitis (having PP is common in MS patients, for those that don't know) and now the bladder issue......should I be concerned about MS? Would I be justified in moving my Rheumy appt up?
So sorry this turned into a novel. I am just concerned. It seems like everyday since my Sjogren's diagnosis, I wake up and it's something new.
Thanks in advance for any replies!
Lisa
I woke up around 3 a.m. to go to the bathroom. On the way to the bathroom I noticed that my sleep pants were wet. When I sat down to pee, I realized my panties were SOAKED!! And my sleep pants were more than just wet! So I emptied my bladder the rest of the way, cleaned myself up, put on dry bottoms and thankfully my bed was not wet! So I laid in bed for over an hour BAWLING!!!! I have been having problems with urgency & frequency lately. But waking up wet....was a first. And I hope the LAST TIME!!!
Some of my "mystery symptoms" include: clumsiness, numbness/tingling in toes & heels, "bee-like" stings on tops of feet, trouble swallowing (despite being on a saliva stimulator) and now the bladder control.
These issues don't happen everyday. I may go weeks without experiencing them. Even then I don't experience all of them.
I see my Rheumy again on 12/12 but I don't know if I should wait that long??? I am dreading going to bed tonight already!! I am already cutting off all fluids at 8 p.m. (I go to bed between 9:30 & 10) and I don't have a UTI or anything like that (just getting over bronchitis & PCP ran blood work and no sign of infection in blood work) and no other signs of infection noted.
So.....what I am getting at is.....since I already have an autoimmune disorder, and I have Pars Planitis (having PP is common in MS patients, for those that don't know) and now the bladder issue......should I be concerned about MS? Would I be justified in moving my Rheumy appt up?
So sorry this turned into a novel. I am just concerned. It seems like everyday since my Sjogren's diagnosis, I wake up and it's something new.
Thanks in advance for any replies!
Lisa