Sjogren’s Syndrome – Introduce yourself and meet others

Posted by cmtg @cmtg, Aug 20, 2016

I have been diagnosed with this and I'm in pain most days and would like to have discussions.

Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.

My eyes & lips symptoms are what made my Opthsmologist & Rheum suspect Sjogrens. The lip biopsy confirmed it.
2 QUs:
#1: Does anyone else with this disease have constantly severely chapped lips? & what do you do for it?
#2: For women— does this affect anyone else vaginally?
Thanks

REPLY
@jerrysgirl3

Labs for all autoimmune diseases and a petscan or brain scan and scan of the spine seem to me to be in order !! I'm so sorry. I know what you mean about the doctors. I get the same thing because I have odd issues going on and I feel like they think I'm faking it.

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So I have swallowing issues. I saw the radioactive dye food go up instead of down, right where I feel that happens. I felt so redeemed, only to find they wouldn't even acknowledge it!
Fast forward six months, and a group of doctors researching colon cancer found a new organ, in the mouth behind the nasal cavity., they are salivary tunes.
Like, how many times do people have to describe something before irs real? The medical literary previously said patients just imagine these sensations...
I guess the infection was all imaginary too 🙃
Newly discovered salivary tubes, look it up, show your friends, it may be in your head, because that's where they're located 😉

REPLY
@tabuschlen

So I have swallowing issues. I saw the radioactive dye food go up instead of down, right where I feel that happens. I felt so redeemed, only to find they wouldn't even acknowledge it!
Fast forward six months, and a group of doctors researching colon cancer found a new organ, in the mouth behind the nasal cavity., they are salivary tunes.
Like, how many times do people have to describe something before irs real? The medical literary previously said patients just imagine these sensations...
I guess the infection was all imaginary too 🙃
Newly discovered salivary tubes, look it up, show your friends, it may be in your head, because that's where they're located 😉

Jump to this post

Omg. I've had issues behind my nasal passages for years and everyone said "it's nothing ". Gotta look it up! Thank you so much!

REPLY
@tabuschlen

So I have swallowing issues. I saw the radioactive dye food go up instead of down, right where I feel that happens. I felt so redeemed, only to find they wouldn't even acknowledge it!
Fast forward six months, and a group of doctors researching colon cancer found a new organ, in the mouth behind the nasal cavity., they are salivary tunes.
Like, how many times do people have to describe something before irs real? The medical literary previously said patients just imagine these sensations...
I guess the infection was all imaginary too 🙃
Newly discovered salivary tubes, look it up, show your friends, it may be in your head, because that's where they're located 😉

Jump to this post

That's like every time I drink water. Only water, my eyes start running tears. How can that be? I also found out that the vagus nerve on left side of neck up to ear causes so many issues I have been having since 2012 where I actually brought it up to the doctors and was laughed at!!! Gets me so angry.

REPLY
@jerrysgirl3

Omg. I've had issues behind my nasal passages for years and everyone said "it's nothing ". Gotta look it up! Thank you so much!

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Nothing like discovering a new body part 2022 , one that many people complain about and describe

Tubarial salivary glands, it was a team from the Netherlands
I saw a unilad article summarizing, couldn't send link

REPLY
@jerrysgirl3

That's like every time I drink water. Only water, my eyes start running tears. How can that be? I also found out that the vagus nerve on left side of neck up to ear causes so many issues I have been having since 2012 where I actually brought it up to the doctors and was laughed at!!! Gets me so angry.

Jump to this post

The worst of this is that the only reason they didn't research this stuff is because they write people off as old or decrepit or something. That's old school medicine for you. So sad you went through that.

Did you hear about the ekectronic therapy to stimulate the vagus nerve? They have a device they can put on the right ear. There are other physio type devices you could set to that frequency as well.
I have robotics and nutrition background, unfortunately gonna need em both to cure/treat this ... no wonder there was nothing else that the doctors can do, they didn't even look into it. And I wouldn't wish autoimmune neurology and gland issues on anyone, it sucks.
Trying to speak up when I find these new treatments because why should people suffer?
I laugh because autoimmune is autoimmune, I have so much overlap with these other things. They should treat all autoimmune with any approved and helpful stuff that would work best for the patient.
So lucky I have MS, because glatiramir acetate does work for me. I just have what damage was done, and now these gland and muscular things because it affected how my brain even makes neurotransmitters.
I read that opioid addicts also have damage to the parts that make neurotransmitters. Such a hard thing to tweak, no wonder they don't know how to heal 😪

REPLY
@tabuschlen

The worst of this is that the only reason they didn't research this stuff is because they write people off as old or decrepit or something. That's old school medicine for you. So sad you went through that.

Did you hear about the ekectronic therapy to stimulate the vagus nerve? They have a device they can put on the right ear. There are other physio type devices you could set to that frequency as well.
I have robotics and nutrition background, unfortunately gonna need em both to cure/treat this ... no wonder there was nothing else that the doctors can do, they didn't even look into it. And I wouldn't wish autoimmune neurology and gland issues on anyone, it sucks.
Trying to speak up when I find these new treatments because why should people suffer?
I laugh because autoimmune is autoimmune, I have so much overlap with these other things. They should treat all autoimmune with any approved and helpful stuff that would work best for the patient.
So lucky I have MS, because glatiramir acetate does work for me. I just have what damage was done, and now these gland and muscular things because it affected how my brain even makes neurotransmitters.
I read that opioid addicts also have damage to the parts that make neurotransmitters. Such a hard thing to tweak, no wonder they don't know how to heal 😪

Jump to this post

I never heard about the electro stimulation of the vagus nerve until i read up on it in a posting here and further research. When I had my thyroidectomy and left neck dissection in 2012, it was a mess. Surgeon didn't do it. His resident did and nicked my vocal cord nerve and left me with Minnie Mouse voice, inability to swallow food. Then I began to experience pain in left shoulder. Thought it might be the vagus nerve (this was all in 2012!) so I took some Percocet from shoulder surgery a year prior. Didn't help my shoulder but it relaxed the muscles in my throat and gave me my voice back after three months!! The drain for the neck dissection was right along the vagus nerve ! He probably nicked that too!! All these years later now I have leukemia and I have nodes going right up my neck up to my ear, following the drain path. I call them my string of pearls. But they are compressing the vagus nerve and causing all different kinds of issues. Sometimes I take muscle relaxers but they cause constipation which I already have a major problem with, having no sigmoid colon. Of course if I tell my endo she'll say it's not related. Maybe I can get my new primary to do something as he seems to listen to me. Having major problems swallowing. Fricking nightmare. And having chronic leukemia which is a nodal disease......

REPLY

Thanks for the information, its good to have...

REPLY
@dianecox

My eyes & lips symptoms are what made my Opthsmologist & Rheum suspect Sjogrens. The lip biopsy confirmed it.
2 QUs:
#1: Does anyone else with this disease have constantly severely chapped lips? & what do you do for it?
#2: For women— does this affect anyone else vaginally?
Thanks

Jump to this post

Yes to both questions

REPLY
@dianecox

My eyes & lips symptoms are what made my Opthsmologist & Rheum suspect Sjogrens. The lip biopsy confirmed it.
2 QUs:
#1: Does anyone else with this disease have constantly severely chapped lips? & what do you do for it?
#2: For women— does this affect anyone else vaginally?
Thanks

Jump to this post

My lips are pretty chapped. I put Vaseline on them nightly.

And yes, I have trouble with vaginal dryness. Always have. Couldn’t wear tampons because of it. I’m 64 now, so she makes it worse.

REPLY
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