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Sjogren's and Other Auto Immune Diseases

Started by mompain, April 18, 2008, 03:09:16 PM

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mompain

I was curious to see how many Sjogren's patients have another autoimmune disease besides Sjogren's, which one(s), what symptoms do you have, and how do you deal with them?

I am asking this because I have POTS (Postural Orthostatic Tacachardyia Syndrome - a form of Dysautonomia) and have recently been diagnosed with Sjogren's.  I also have Fibromyalgia but I do not think this is considered an autoimmune disease.  I would love to hear how you cope with these illnesses and just some things you could offer in the way of encouragement or any things that you have done that helped you better manage your illness.

Thank you in advance for any comment or help you would be willing to offer.

Tamik

I have Pernicious Anemia in addition to Sjogrens. I get B-12 shots regularly as well as physical Therapy to strengthen my neck muscles -they are not strong enough to hold my cspine in place I guess... Still asking why - could be because my B-12 was low for so long...  Also have Fibromyalgia.  How am I coping?  I am taking each day as it comes and finding the joy in it -I find something to look forward to each day.   THe only meds I am on is an acid blocker for the burning esophogus, vitamin D, and the B-12 shots.  Usually I feel O.K. -I do take a nap everyday as i work from home -the fatigue is the worst -that and the neck and headaches right now.  I was told I probably had the Pernicious Anemia my whole life - but wonder if that is true or if Sjogrens had something to do with it.  The most frustrating part is finding a doctor who doesn't think I am crazy and who will really listen! My rhumy just shakes her head when I am talking and says see you in 6 months - last time as seh walked out the door she said "Oh -you do have antibodies for that and you need B-12" and continued into the next room with another patient.  I found out from my GP that I have pernicious anemia!  Tami K 

Scottietottie

Hi Mompain  :)

I have Sjogrens/lupus overlap and Hashimoto's thyroiditis. All definitely AI diseases. I also have irritable bowel and irritable bladder syndromes and osteoarthritis.
I cope by taking every day as it comes and trying to have a laugh and I have a long sleep every Sunday.

Take care - Scottie  :)
http://sjogrensworld.org/   (our home page)
http://www.sjogrensworld.org/chats.htm   (find our chat times here!)
https://kiwiirc.com/client/irc.dal.net  (way to chat + nickname and #Sjogrensworld)


Never do tomorrow what you can put off till the day after tomorrow!

Linda196

Mompain, I have Hashimoto's thyroiditis, Raynaud's, dermatomyositis, autoimmune vasculitis, rosacea and Sjogren's...all autoimmune diseases; plus sarcoidosis, an immune response disease. I also have IBS and fibro, which aren't AI, but are linked to AI much of the time.

I never really thought about how I cope...I just do what needs doing, and when I have a chance, I rest or pamper myself somehow. I suppose one way that I "cope"  is by learning to redefine "what needs doing"...it was a bit of a surprise to me, but I discovered that I'm not solely responsible for the world spinning on its axis, and things move along just fine without my input!
Please check out our home page at http://www.sjogrensworld.org/index.html {{INCLUDES A LINK TO AMAZON SHOPPING!!}}
; and live chat at https:https://sjogrensworld.org/index.php?board=30.0

Rania

#4
I have several autoimmune diseases too. It started out with one, then the rest came along.
Quite normal according to the docs I've seen.

Rania  :)

irish

Mompain, I have Sjogrens, Myasthenia gravis, Hashimotos, Bullous Pemphigoid(skin AI), Asthma and low T-cells and very low IgG subclass 1 and 3 which are also part of the white cells etc that help fight infections. The doc thinks the T-cell problem is most likely hereditary but could be autoimmune also. I am 65 years old and have not had good health for many years including when the kids were little.

I just plugged along and rested as much as I could, went to the doctor only to be told it was "my nerves". I also worked part time as a nurse and did a lot of work outside on our hobby farm. Sometimes I felt like I would die standing up but I never died to I just kept on working. lol

Finally got diagnosed in 2003 and 2006 and since November 2006 I have been on monthly IVIG Gamunex for the myathenia and the t-cells. I can't take the DMARDS. Now I do what I can when I can and just get up and am thankful for each day. Don't get out a lot socially as I seem to not do well in crowds with my right sided deafness and fatigue factor. If I have too much fun I pay dearly for it the next day with increase in myasthenia symptoms of weakness and occasionally affects my breathing.

I just enjoy the things that I can do. Read a lot and like to cook and love to shop. I hang on the cart at the stores and rest when I need to. I told hubby the other day that when the kids were young I couldn't shop for long periods of time as always had to be some place to pick up kids etc. Now I have no set schedule and I just love to look---can't afford to buy that much but just enjoy being out of the house. Irish ;D

wordnerd

These AIs seem to come in groups, don't they?

Let's see... I've got

AI Pancreatitis, AI Hepatitis, Hashimoto's, Fibro, Seizures, Asthma, Sleep Apnea, IgA deficiency, Raynauds, Erthymyalgia, Tremors, Migraines, Autonomic "weirdness", motillity problems, bladder problems, GERD, and more I can't think of right now

which, according to my doctors are all thanks to Sjogren's

mindytyson3

Ok so I just got diagnosed with Sjogren's. Will I end up with another autoimmune disease? Or could I just stay with just one? lol.

slccom

You could stay with just one. Keep in mind that the people who post to these boards are the sicker ones. A lot of people check it out, find their answers and don't need more support.

Sharon

Styx

I remember 7 years ago, I came to this board with nose and GI problems and thought "ok, I know I'm sick, but these people are hypochondriacs. There is no way that these people contract so many distinct, albeit related, diseases."

7 years later, I'm now one of you all, and I know the hard way that you all are not hypochondriacs nor am I. I suppose that's poetic justice for my ignorance.

I now have eye, nose, GI, lungs, skin, and mouth symptoms :)

Styx

Duchess

Sjogrens, Lupus, Raynauds, GERD, Interstitial lung disease, Asthma, Chronic constipation, Overactive bladder.


Duchess
58 y/o, Sjogren's, Lupus, Raynaud's, Mitral Valve Repair, Asthma, Myofascial Pain. Plaquenil, Inhalers, Ibuprofen,Exovac, Vitamin D, Vitamin B-12, Omega 3, Eye Drops, Quinipril, Massage therapy.

Diane54

AI Hepatitus,  Antiphospholipid Syndrome, Hypothyroid, Diabetes, Raynalds, and RA...just to name a few!
Sjogren's diagnosed Dec 20, 2010, Hypothyroid, Diabetes 2, Autoimmune Hepatitis, Mitral Valve  Prolapse, Gerds, Antiphospholipid Syndrome,  Synthroid, Paxil, Prilosec, Evoxac, Plaquenil, Tramadol, Simvistatin, Restasis, Baby Asprin, vitamin D, Januvia, Amlodipine, Gabapentine

jpd54

I have SJS, Fibro, Osteoarthritis, Osteoporosis, GERD, chronic constipation.  So much fun!!!!

                      Jennifer
SJS, Fibro, Osteoarthritis, Osteoporosis, GERD, Rosacea, TMJ

Celebrex, Gabapentin, Lasix, Potassium,Hydroxychloroquine, Lexapro, Lisinopril / Hydrochlorothiazide, Linzess, Metoclopram, Nexium, Oracea, Savella, Simvastatin, Vitamin D, Voltaren

cargillwitch

I have Primary Sjogrens and Raynauds; also have gastroparesis and IBS as well as degenerative disc disease.

I cope by doing things i enjoy with people I love. I love to be outside, hiking gardening and spending time with animals.
I also blog, its another form of catharsis!
47 female, Sjogrens ,Raynauds,degenerative disc disease.Rheumatoid Arthritis, gastroparesis.

MaryBee7

Was told I have RA...then polyarthritis...then Chronic Fatigue Syndrome brought on by EBV.  Now Primary Sjogren's with a gut that is threatening mutiny.  I think Brain Fog should be its own AI disease!  It certainly is enough to handle by itself.