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.

@lisalucier

Hi, @gemmax and @mickie75 -- I wanted to introduce you to some of the members on this site who have talked about Sjogren's syndrome -- in themselves or in a loved one -- here in this discussion or elsewhere in the Connect community, such as @cmtg @kibwezi @marylou705 @peach414144 @johnwburns @oldkarl @devonsdad2008 @graveltruck @jewel8888 @sebley12 @briansr @frank1 @ccorrconro @mswanda @bettyjeanne @kkteel1 @66andcounting and others.

@gemmax and @mickie75 -- wondering if you'd tell a bit about your story with Sjogren's, and hoping some of the others here might introduce themselves and lend a hand with any challenges you are experiencing with this syndrome.

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@gemmax True. I have always had the 'Village' mentality. We humans are by nature social beings, and are where we are today (not in caves) by standing by one another.

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@gemmax

@peach414144 When I was working on my genealogy, I found a 3xgrandmother who was a slave..born into it after her mother ws taken from Mopzambique. I sat down and cried for her and her mother and younger sisters and brothers. Her burial place remains unknown as does my 3xgrandfather, a european . I still cry for the atrocities of man. I take some solace from these words from Ecclesiastes 12:7 "Then shall the dust return to the earth as it was: and the spirit shall return unto God who gave it.” It is my belief that God knows us all. Our legacies, our prayers are not lost. I can't know your pain, but I can care about all the lives that have been lost to evil. Be blessed.

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@gemmax Sounds like you have an interesting lineage. I have a photo of an oil painted portrait of one of my great greats going back to 1470. His face and hair look exactly like me. When I show it to friends, they think it is me and that I had it done at one those boardwalk shops. You know the ones that take sepia tone old-timey photos? It was bizaar to see such a strong resemblence after so many generations.

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@gemmax

@peach414144 When I was working on my genealogy, I found a 3xgrandmother who was a slave..born into it after her mother ws taken from Mopzambique. I sat down and cried for her and her mother and younger sisters and brothers. Her burial place remains unknown as does my 3xgrandfather, a european . I still cry for the atrocities of man. I take some solace from these words from Ecclesiastes 12:7 "Then shall the dust return to the earth as it was: and the spirit shall return unto God who gave it.” It is my belief that God knows us all. Our legacies, our prayers are not lost. I can't know your pain, but I can care about all the lives that have been lost to evil. Be blessed.

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@windwalker I have a large family, but I look different from most and had always wondered where my appearance came from. Then I came across a gggrandmother who is ¾ cherokee and although my skin is English like my mother, I looked so much like her that I couldn't believe it. I loaded the two pictures one of her and one of me on top of each other in a program that i have and changed the transparency and there we were a perfect match! I find genealogy very interesting. I started years ago and collected documents as i went along. I love to restore old photos too.

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Gem...Where did you learn all these things like genealogy and restoring old photos. Did you take classes or teach yourself

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@gemmax

@peach414144 When I was working on my genealogy, I found a 3xgrandmother who was a slave..born into it after her mother ws taken from Mopzambique. I sat down and cried for her and her mother and younger sisters and brothers. Her burial place remains unknown as does my 3xgrandfather, a european . I still cry for the atrocities of man. I take some solace from these words from Ecclesiastes 12:7 "Then shall the dust return to the earth as it was: and the spirit shall return unto God who gave it.” It is my belief that God knows us all. Our legacies, our prayers are not lost. I can't know your pain, but I can care about all the lives that have been lost to evil. Be blessed.

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@gemmax I find genealogy very interesting as well. I think it would be great to also have health history in that data bank so that future generations can learn what to watch out for.

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@johnwburns

Sorry to hear that.
Sjogren's is a big topic.
How were you diagnosed, as in what were the criteria, positive ANA, positive anti-Ro, salivary gland biopsy etc?
What treatment(s) have you been given, if any?
Do you have any commonly co-occurring autoimmune illnesses such as Hashimoto's Thyroiditis?

Overview might be of help:
http://www.mayoclinic.org/diseases-conditions/sjogrens-syndrome/basics/definition/con-20020275
Thanks

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I have just been diagnosed with primary Sjogren's via a lip biopsy. I was Ro and La negative. I have very dry eyes which I am managing reasonably well with eyedrops and dryness down below which I am using topical oestrogen for, I have been started on Pilocarpine (Salagen) 2-3 times a day. I was led to believe that I would not get any systemic symptoms but I do have some symptoms of fatgiue - not crippling but enough to make my working life difficult, I am 53 years old and have been told the fatigue is just part of the menopause but I am not convinced. What are the best ways to help with the fatigue or is it just a case of accepting it and pacing yourself? Any advice would be very much appreciated.

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@colleenyoung

Welcome to Connect @cmtg. You have landed in the right place. I'd like to introduce you to a few other members who also have Sjogren's. Please meet @johnwburns @blindeyepug @meemer @kyjeanne @uncbball and @ccorrconro for a start. I'm confident others with join this discussion too. I also encourage you to browse the other discussions in the Autoimmune Diseases group https://connect.mayoclinic.org/group/autoimmune-diseases/

CMTG - why type of pain do you experience and what methods or treatment do you use to try to manage it?

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Dear

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@johnwburns

Sorry to hear that.
Sjogren's is a big topic.
How were you diagnosed, as in what were the criteria, positive ANA, positive anti-Ro, salivary gland biopsy etc?
What treatment(s) have you been given, if any?
Do you have any commonly co-occurring autoimmune illnesses such as Hashimoto's Thyroiditis?

Overview might be of help:
http://www.mayoclinic.org/diseases-conditions/sjogrens-syndrome/basics/definition/con-20020275
Thanks

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I was diagnosed by lip biopsy and I have a dry mouth and dry eyes. I use eyedrops regularly and also take Pilocarpine (Salagen) to help my salivary glands be more productive. I have no other auto immune diseases. I was diagnosed a year ago but have had dryness symptoms for many years. I was Ro and La negative on a blood test so my rheumatologist is hopeful that I will not develop the joint problems and tiredness.

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@johnwburns

Sorry to hear that.
Sjogren's is a big topic.
How were you diagnosed, as in what were the criteria, positive ANA, positive anti-Ro, salivary gland biopsy etc?
What treatment(s) have you been given, if any?
Do you have any commonly co-occurring autoimmune illnesses such as Hashimoto's Thyroiditis?

Overview might be of help:
http://www.mayoclinic.org/diseases-conditions/sjogrens-syndrome/basics/definition/con-20020275
Thanks

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Jean,. Good news for you. I have had RA for at least 10 yrs. The drugs are hard on me. I try to get thru the episodes with only Tramadol. Very very light drug. Recently my ocologist is finding something suspicious in my blood. He is not ruling out multiple Myeloma. I am doing one more blood test which somehow was damaged. I truthfully believe I do not have Myeloma. I suspect what you have. I fogot the name of disease. We can survive that. I am so sick of taking pills and being so tired and low energy. God Bless. Lee

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@cmtg

I have all the symptoms above you described except never had a lip biopsy, Dr said not needed, the diagnosis is pretty clear. It took seven years for diagnosis. I guess did't make myself clear to you.

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I find it so hard to accept the time it takes doctors to determine disease. What are they teaching in dr school. I have had so many hard to stand tests with promise that after THIS test we will have a determination. They never do. I must have a new disease or need new doctors.

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