Pommy g'day ... is it really sjogrens? - The Australian Sj...

The Australian Sjögren's Syndrome Association

2,436 members779 posts

Pommy g'day ... is it really sjogrens?

Polly2Cats profile image
4 Replies

G'day (sorry couldn't resist)

I'm newly diagnosed with sjogrens... About 4 hours ago! 

I'm afraid to say it makes no sense to me or my GP we both feel I've got more lupus symptoms.  

I'm awaiting saliva gland biopsy (my mouths a little bit dry but no swallowing issues) I've got a little bit of a dry eye (but I can wear hard contacts for 18 hours no bother) and the gynaecologist assures me that's not dry either. 

I've had some blood tests and that's how the diagnosis was made. 

I've had an injection to dampen my immune response and can start hydroxychloroquine if that doesn't help. My worst symptom is the fatigue. 

Does this sound like sjogrens to you guys? Any advice please?

Thanks in advance 

Written by
Polly2Cats profile image
Polly2Cats
To view profiles and participate in discussions please or .
Read more about...
4 Replies
HollyHeski profile image
HollyHeski

You dont say why you had the blood tests but yes,  even though mild symptoms with mouth & eyes, sounds like SS.

Megansheart profile image
Megansheart

Also you don't say what blood tests you had done. Did you have ENA's done (Extractable Nuclear Antibodies)? If so, which of those came back positive? If not, did your ANA's come back positive?

There is quite a lot of overlap with symptoms with Lupus and Sjögren's and fatigue is common with most autoimmune conditions.

You have to be guided by what the clinical symptoms are, the blood tests and from there your doctor. Hopefully your GP will refer you to someone who is more specialist in autoimmune conditions like a Rheumatologist. Who prescribed you the hydroxychloroquine?

G'day to you from an Aussie Sjögrens (most probably).

Polly2Cats profile image
Polly2Cats in reply to Megansheart

I'm embarrassed to say I don't know what blood tests I had or the results. My partner couldn't join me at the appointment due to short notice and I was just told ss and drawn a very patronising picture! I'll talk to GP as suggested. Thanks 

Tassa profile image
Tassa

Sounds very much like SS or Lupus of which I have both. If you have either or both your whole system will probably end up dry inside and out. keep your fluids up and drink water, when  I was first diagnosed I was suffering from severe loss of energy a dry mouth and eyes also skin. I was advised to take a natural product called Mannatech which rejuvinates the cells in your body. I have been on it for 5 years now and am off all medications that have side effects. I live in New Zealand and it is not available here but I order it from Australia. I take the powder form ambrotose and the tablets called Plus. They take awhile to kick in but if you decide to try them you must stay on them don't give up as they need time to work on your depleted system.

They are not cheap but have made a very big difference to my lifestyle in the fact that I have got my energy levels back and can now walk and ride my bike and lead a normal LIFE again. It may also help to take a vitamin and mineral addition as people with auto immune problems are lacking in that quarter. It will not help the dryness but will give you a much better quality of life. You can take this product as a health booster with any illness you may have. Google Mannatech it may be available in other countries beside Australia. Good luck. 

Traveller.     

You may also like...

Sjogrens or not?

pain with morning stiffness , irritable eyes, dry mouth and terrible tiredness for 4 years, i...

Sjogren's or kidneys?

I have finally got a date for my salivary gland ultrasound - but whilst I was waiting I had to see...

Sjogrens or allergies ❓❓❓

wonder if anyone with SS experiences nasal issues ? I'm on Plaquenil and the paresthesia is better...

Sjogren's Syndrome and Coeliac disease.

I've had Sjogren's for over 20 years now and am having issues with bloating, IBS, and food...

Sjogrens and pancreas pain

it's primary SS or not (I'm sure I've had them done before - maybe not - - I've had so many bloods...