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Hi StabbedBadger (Steve)
I have left a message on your last post in discussion regarding employment.
greetings from the Limpopo Mountains. I am a 49 yo Brazilian artist currently living in South Africa. I am privileged to spend these crazy times in an incredible landscape with amazing non-human animals! If anyone needs a "burst of fresh air" I can send some pictures!
I've been suffering from Chronic and joint pain for at least 10 years, but only this year after severe flare up that made me loose movement in my hands have found a rheumatologist who diagnosed me with RA and urged me to start treatment (and was very blunt when I told her I've gotten used to live with pain... "but now your age won't let you"! ) . Previously I was diagnosed with fibromyalgia, stress, PTST... and tried some drug treatments but mostly relied on exercise, diet and alternative therapies. I have been on Sulfasalazine and Methotrexate for a month now and coincidence or not flare up is gone and serious decrease of pain. On the other had I am suffering with nausea, lack of appetite and really bad stomach pain. Also lotsa of pimples! :(
Looking for tips and ideas on dealing with it! Good day to all!
Welcome to the forum - it's great to have a member from South Africa, we have other European members and some from Australia too!
Now you are on Sulfasalazine and Methotrexate your RA is controlled but you are feeling sick and have stomach ache and no apetite and some spots.
They do sound like side effects of Meth and Sulfa - I'm going to include links to those meds, but the best thing to do is get back onto your rheumatologist and explain, there are remedies - taking folic acid or moving to meth injections perhaps.
I'm sure these will help you check the side effects you are having, do let us know how you get on your appointment - I shall be looking out for it!
thanks for your message. I have already checked the links, thanks. it does feels like side effects. unfortunately won't be able to see my rheumatologist as we are going back to stricter lockdown and interprovincial travel is not allowed, but trying to contact her online. I am already taking folic acid (and lots of ginger tea!) and unfortunately medical aid won't cover meth injections, that's why I am curious to know more from other people who may have experienced the same. will check the other groups ! thanks again. have a good week x
Good to meet you welcome to this lovely community.
Sorry to hear your MTX is causing some side effects for you. Top ten tips are (in my non-professional opinion!) rest rest and rest g=again the day afterwards and eating savoury seems to help a little too. If you only have folic acid once a week that might be incresable if your Doc agrees.
When we are in 'proper' lockdown (and still pretty well here) we couldn't see our Drs either on the whole, but video apts and telephone consultations are doable now.
Might be worth sticking Methotraxate side effects into the search box and see what that throws up?
Greetings! Jump in and natter away. A photo of your dog in Pets Corner would be nice, although I am a cat person.
Hello and welcome to the forum @DonnaC
I am sure you will find information and support from other forum members.
It sounds as if you are doing all the right things, speaking with your GP and physio. Neck pain can be really debilitating, and worrying if it is affecting your ability to drive. For some types of inflammatory arthritis there are blood tests that can show markers. There’s no blood test for osteoarthritis, although your doctor may suggest you have them to help rule out other types of arthritis.
X-rays aren’t usually helpful in diagnosing osteoarthritis, although they may be useful to show whether there are any calcium deposits in the joint. You could ask your GP or physio if they feel you require further investigation into your symptoms.
I have added some links below to information on our website:
Understanding neck pain,
Exercise and arthritis
Driving and arthritis
I hope this information is of help.
I'm sorry to hear of your problems with MTX
I tried methotrexate twice and couldn't handle it at all,15mg per week gave me bad nausea,headaches and made me feel really down and "off".I tried to stick with it,tried folic acid every day apart from mtx day,ate crystallised ginger etc but then I developed cough and breathlessness so was taken off it for a while then restarted at only 7.5mg which made me feel just as bad.
I had to come off it,I felt a bit of a failure as I know of 2 other people in my village who take it with only minimal discomfort but the rheumatology nurse said it doesn't suit everybody, 1 in 10 can't take it.
Hopefully as time passes the side effects will ease for you as you say it is helping your arthritis.
Do let me know how you get on.
welcome to the forum, it's good to see you here.
You have fibromyalgia, arthritis in your knee and Raynaud's phenomenon. If you haven't already, it's worth having a look at the information on our website, which may answer some of your questions and raise others.
If you are worried or feel that you need to talk through some of the issues around your arthritis, please phone our Helpline team, who can help you look at some of the information that's out there and possible support.
And, of course, the online community here will have many members who have experience of some or all of your own diagnoses.
Good luck, Julie and we look forward to seeing you here.
May I share my story, of hip problems.
I am a 42yr old electrician and for the past few years hip pain has slowed my extremely active lifestyle down and affected my work. I would always be running around, dancing, gardening and cycling everywhere. To be honest I have used exercise, over the years, to deal with low mood. 3 Weeks ago while lifting a large heavy box I experienced sudden pain my right hip. I got checked out at hospital and the x ray showed slight progression in osteoarthritis from an x ray 4 years back. I was prescribed exercises and pain relief. I continued working and on Friday while lifting, I had another sudden pain incident in the right hip, which felt far worse than the previous one. I went to A+E, where the prescribed more exercise and pain relief.
The early hours of the next morning I woke in great pain, got up to relieve myself and my partner found me passed out in the toilet. An ambulance team arrived, they ran some obs tests and took me to the hospital. This time they took several x rays and blood tests. The young nurse shared how she believed fainting is a thing with severe hip pain.
The doctor in the hospital said that because I could ambulate (walk) and my pain (whilst not moving was moderate) they would have no choice but to discharge with a referral request sent to my GP albeit an urgent one. So I may get an specialist osteo appointment in a couple of weeks rather than a few months which I had been told after the first incident.
I have built my whole life and career around being physically fit and now this last week I am now wondering what I will be able to do.
I am disappointed that I was referred back to the GP as my business and therefore whole life are on hold. The hospital doctor said that joint problems are one of their most common patient complaint and that criteria for immediate referral are;
-severely restricted joint movement
-high level pain etc.
but not the need to make a living seemingly!
From my perspective I argued that, yes the phsio could manipulate the joint, and I am able to hobble with crutches, but the severe pain comes when under load, particularly when bending. I am unable to resume actively running my business and as the last 3 weeks experience has demonstrated, carrying on as usual with supplementary exercises and pain relief has not helped and in fact brought the issue to a head.
As I said to the doctor, it seems you have to be practically crippled to qualify for treatment, ie an MRI and who knows then possibly, surgery, yet wouldn't prevention be better than cure? Or do I now throw away my business, all the training, let my apprentice go, and try to start a new career which accommodates limited mobility? Desk work etc?
I will wait and see what the GP says in the next week or two, and make use of this forced rest to do my tax return.
I know it is early days but my gut instinct is telling me this is not a rest and recover situation now.
Thanks for hearing my story and I look forward to learning about these conditions with others.
Welcome to our forum. Here you will find our members are friendly, empathic and will offer you answers to your queries and problems as they have been related to their own conditions.
You are going through a tough time at the present with your hip pain. Versus Arthritis have produced many booklets and leaflets related to arthritis and related conditions. Below you will find links which you may find useful:
There is a Versus Arthritis freephone helpline where you can speak to someone one to one. it is : 0800 5200 520 (Monday to Friday 9am to 8pm) The only thing to remember no one on the helpline or on this site are medically trained.
You have an appointment with your GP in the near future. It may help you to make a list of the things you need to ask him so that you do not forget something that is the most important thing. Also it may be helpful for your wife to go with you, so she can remember what the doctor has advised you to do. When people go to the doctor's they sometimes forget points that he has said to you, having someone with you means that they can help you if you are a little hazy about what he has said.
I look forward to reading your future posts and reading how your getting on. Take care.
Welcome to the forum,lovely you have found us.
You say that you have only been diagnosed with PsA a couple of weeks ago and you had a steroid injection at the same time, but the knee has had a flare up again.Firstly I would go back to your Rhumatologist for the flare up to see what else they can do. I also have a link with some information that may help youhttps://www.versusarthritis.org/about-arthritis/conditions/psoriatic-arthritis/
Take a look round our forums the most popular being Living with Arthritis, Chit Chat and Vals café.
please let us know how you get on Christine
Hi I’m Alex and I’m 26. I have arthritis in my hip and spine still going through diagnosis. My dad and nan have severe arthritis which has led to wheelchair use and joint replacements and honestly I am a little scared I am going the same way because I have a 9 year old and I want to be a fun mum. I’m hoping to talk to people who can support and help each other 😊
Welcome to the forum good to see you contacting us
You say you have Arthritis in your hip and spine and still going through diagnosis.
Here is a link that may help in explaining what is happening to you.https://www.versusarthritis.org/about-arthritis/conditions/osteoarthritis-oa-of-the-spine/
also on the forums you will find people who are going through what you are at this moment.
I remember being pretty scared after I was first diagnosed so I know what you are going through.
the most popular forums are Living with Arthritis, Chit Chat and Vals café.
Please let us know how you get on.
I am 64 years old, had arthritis in both my hips and both hands for over 15 years. It has been not only painful but debilitating as I am sure you all understand.
I am going to keep this short and sweet, I have tried many different treatments over the years and nothing has really taken even the edge off. 3 months ago my son was talking with his naturopath, he told her about my arthritis and she told him that I should try cannabis oil. From the first day I tried the oil within 2 hours the pains in both my hands were gone, however I put that down to me wanting it to work (placebo I have just been told is what thats called). However, I have now been taking the oil for 3 months and it has changed my life. I don't feel any pain at all now (touch wood) and I have not slept like this for years. My brother now takes the oil and so does his daughter (both also have arthritis in different areas) and they would tell you that what I am saying here is gospel.
I wanted to share that because, I am sure there are people who have had enough of the constant bleeding nagging pains it causes, my moods have been so much better (my wife will testify to). I could not recommend the oil highly enough.
Hi @Jayman29481 and welcome to the Versus Arthritis forum.
So you have been suffering with arthritis for over 15 years and have found that cannabis oil, which you started taking 3 months ago, has helped alleviate your pain.
For your benefit and those of other forum members Versus Arthritis’s thoughts on Cannabis Oil can be found here https://www.versusarthritis.org/news/2020/march/complementary-treatments-and-arthritis-from-turmeric-to-cannabis-oil/
Here is an extract:
“Cannabis oil (CBD)
CBD is type of cannabinoid – a natural substance extracted from the cannabis plant and often mixed with an oil (such as coconut or hemp) to create CBD oil. It does not contain the psychoactive compound called tetrahydrocannabidiol (THC) which is associated with the feeling of being ‘high’.
Research in cannabinoids over the years suggests that they can be effective in treating certain types of chronic pain such as pain from nerve injury, but there is currently not enough evidence to support using cannabinoids in reducing musculoskeletal pain. We welcome further research to better understand its impact and are intently following developments internationally.
CBD oil can be legally bought as a food supplement in the UK from heath food shops and some pharmacies. However, CBD products are not licensed as a medicine for use in arthritis by MHRA (Medicines and Healthcare products Regulatory Authority) or approved by NICE (National Institute for Health and Care Excellence) or the SMC (Scottish Medicines consortium).
We know anecdotally from some people with arthritis, that CBD has reduced their symptoms. If you’re considering using CBD to manage the pain of your arthritis, it’s important to remember it cannot replace your current medicines, and it may interact with them, so please do not stop/start taking anything without speaking to a healthcare professional.”
If at any time you fell it would be useful then please do call our free Helpline on 0800 5200 520, or email [email protected] (Mon - Fri 9:00am – 8:00pm) if you ever feel they could be of help.
Thank you for your message.
I just wanted to share my experience as I felt obliged to.
Just to say Hi, and looking forward to joining this forum.
Hi @Bex and welcome to the online community.
There's a lot going on here, and the members are friendly and wonderfully helpful. Would you be able to tell us a little more about yourself and how arthritis affects you?