Struggling with work, how does everyone with SS cope?
Posted , 6 users are following.
This is the first forum I have joined since being diagnosed with SS and rheumatoid arthritis. Just looking for anyone's experiences or thoughts on the disease as I feel trapped between a rock and a hard place.
I have just started taking Quinoric and already experienced stomach pain and diahhorrea meaning having to leave work early and iv only been taking them a few days! I already suffer with terrible fatigue and barely make it through the day at work. I rarely attend social gatherings or end up cancelling last minute due to feeling generally awful. I would love to cut down my hours at work but cannot afford it, especially now I have the extra dental check ups, eye tests, prescriptions etc to pay for, nevermind the unpaid sick days I have had to take up to now. I am left drained and totally fed up from the beginning through to end of each day! Any responses would be gratefully received!
0 likes, 11 replies
morelia100 jennifer84972
Posted
lily65668 jennifer84972
Posted
Reactions have been varied, with some people reporting that it helped their symptoms. However, my general impression is that more people stop taking it because of side-effects than benefit from it. But that's just anecdotal.
I'm retired now, but was about 50 and in a very demanding job when my SS started, and only 37 when I had my first attack of RA. I had to take a couple of weeks' sick leave during that first flare-up of RA, but a homeopathic rheumatologist fixed the problem, and none of my subsequent flares of RA have ever been as bad.
Fortunately, my SS didn't interfere significantly with my working life, though it made me feel pretty miserable at times. But then I think I must have been lucky, because I didn't suffer unduly from fatigue.
Like Morelia, I just learned to work around it, working out what triggered my symptoms - mainly in the area of diet - and avoiding triggers.
I know a couple of people on this forum are going to shoot me down for saying this, but don't assume you'll always feel as bad as you do now. You don't say how long you've had SS, but in my case the first few years were the worst. In the 22 years since my first symptoms I've had several almost complete remissions and a lot of periods when my symptoms were quite bearable. I actually feel better in general now, at 72, than I did at 50.
sally83545 jennifer84972
Posted
Don't give up on the meds it takes at least six months to kick in the first month is the worst. Most side effects go away within six weeks. I take 400mgs and split the dosage half in the morning half in the evening... A lot easier on the side effects. Try to change up your diet to reduce stomach issues .you will be amazed how much better you will feel and how much energy you will have I am so much better now..started the meds August of 2014. Try to rest when you can, drink lots of water with the meds. You just have to power through the next few months. It does get better! Good luck
Sally
daniw83 jennifer84972
Posted
I feel for you. I'm recently diagnosed with SS and I get the aches and Pains tirdness & fluy feelings. As well as the peripheral neuropathy. Which is horrible. I do Office work and my right arm is constantly in pain Like its always swollen. I've changed my diet and been taking some vitamins. I was on hydroxychloroquine but i was alergic to it. Rhumy won't give me anything else but to be honest I don't really wanna go on any of that nasty medication so I'm hoping that eventually I'll just be able to put up with the pain. Do you get any support at work ?? Like extra breaks etc.
shaq26875 jennifer84972
Posted
He precribed hydroxychloroquine (plaqunil) to be taken 2x a day (morning and evening). It certainly helped my joints and saliva. I took myself off all meds I was on including plaqunil a few months later. My joint pains come and go but nothing I cant live with and if it gets bad i take panadol or brufen (at bed time) I think I am lucky that my SS symptoms are not bad as some of the others.
I hope your symptons lessen over time.
jennifer84972
Posted
I knew there was something not right around this time last year, my glands kept swelling and were so painful I couldn't eat, I also have the usual symptoms, dry stinging eyes, dry mouth, aching joints, fatigue. I was then referred for blood tests and an ultrasound on my glands, the blood tests showed positive for sjogrens and I have a high inflammation rate. I eventually got an appointment with a rheumatologist around five months later and have been prescribed the Quinoric to ease my asking joints and fatigue.
I'm only 27 years old and have a good job with a mortgage and bills to pay, me and my partner would really like to get married and try for a baby next year and I've been told by the rheumatologist Quinoric is safe to keep taking.
I will certainly take everyone's points and tips on board to striving for a brighter more positive future, definitely cherishing the days I feel near-ish normal! Still just trying to decide whether to continue with the Quinoric or not, such a hard decision, but I will definitely make some diet and exercise changes,
Thanks again everyone,
Jen x
daniw83 jennifer84972
Posted
Its hard isnt it. Im only 32. as SS has so many symptons & trying to explain to friends & family they dont get it.
I hear ya with the looking forward to near normal ish days 👌
Mail me anytime
Danielle xxx
jennifer84972
Posted
Thanks again,
Jen x
daniw83 jennifer84972
Posted
Pain in my right arm is unbearable. It feels like it takes me for ever to type or do anything its like constant toothache do you really not get any extra breaks. My work is not very helpful they dont like it when you ask for things to be put in place. Im waiting for a oh appt to see what they say xx
Xxx
lily65668 daniw83
Posted
I think you should see your GP about this, but without bringing up the Sjogrens connection, as this might put him off the scent and cause him to disregard it. A trapped spinal nerve is a relatively frequent occurrence, and can happen to anyone, not just SS sufferers. It can affect one or, more rarely, both arms. I'm not actually sure there is a connection with SS anyway. My second attack came last year, at the height of a Sjogrens flare-up, but my first attack was when I was 32, five years before I developed RA and nearly 20 years before my first SS symptoms.
If it is a trapped nerve, wearing a foam collar during the day for a few weeks will help a little. My GP ordered an MRI, which confirmed the diagnosis, but I realise this might not be on offer if you're in the UK, or too expensive if you're in the US. I only had to wear the collar for about six weeks and am just coming to the end of a course of physiotherapy to try and improve my posture, which is a contributing factor. I was also able to identify something I was doing which was making it worse.
If it's any consolation, a trapped nerve usually frees itself in the end, and the pain clears up.
daniw83 lily65668
Posted
I've had my cervical MRI and it came back that there was no trapped nerve. Nerve conduction study and EMG said problem in C7C8 area. Neurologist said EMGs are not very reliable and there is nothing he can do apart from the refer me to a pain clinic. (Apt in 4 weeks). Bit sceptical as I've heard mixed reviews about pain clinics. Also had wrist MRI Said ive got to much fluid in the hand & an inflamed tendon. They gave me a steroid injection in the wrist but it didn't really do anything so i dont no what they going to do next. Xx