Reactive Arthritis :: Swimming And Cycling Best Excercises


Dec 4, 2008

Like others here, I've had periodic reactive arthritis since the age of 10. I'm now 33. If you're not into swimming then cycling is in my opinion the best alternative exercise for joints, probably because you're not jarring the joint, or causing undue stress, the same as with swimming. I cycle to work every day, ten mins each way, and it really helps the early morning pain in my knee. The docs say to me 'if it's not causing more pain or swelling then do it.'

My left knee has always been the problem joint and the swelling always impresses even the most experienced orthopaedic specialists. In the past I regularly defied doctors advice and played football once the swelling had subsided enough to make movement comfortable, though the knee is always huge again the next day and has taken a week or so to reduce in size.

I'm now in the middle of another bout of Reactive Arthritis (from food poisoning abroad, which is nearly always the trigger for mine). I was on crutches for 2 weeks, though not hospitalised this time and am not going to risk a set back in recovery so am resisting the urge to play football this season. This arthritis started in April and from experience I'm hoping to see the swelling settle down in the Spring. Takes around a year for me each time. For me the key to getting through is to keep as active as I can with a gradual increase in sports until the swelling reduces completely, while not pushing too hard too soon.

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Low Fat Diet - Treatment Of Reactive Arthritis

I am a woman of 56 and have never been overweight and up to these eleven years ago enjoyed good health.

My first symptoms started eleven years ago whilst on holiday in France. My elbow and knee joints became difficult to move and painful, particularly when carrying shopping. A fortnight later on my return to England the pain had increased, my ankles had started to swell and I felt generally very unwell, not unlike an onset of influenza. My doctor thought it may have been an insect bite and prescribed a course of antibiotics which had no effect. He then tested me for Lyme's Disease and put me on a further two courses of antibiotics, none of which made any difference. The Lyme's Disease test was negative.

By this time, six weeks from the first symptoms I was almost bed-ridden. The joint pains were almost unbearable, I felt itchy all over and isolated little bumps that were extremely painful to touch appeared under my skin, two on my hand and one on my rib bone. After a couple of days they disappeared and I was left with bruises. Some of my knuckle and finger joints were swollen and started to become slightly deformed. I found that I was passing water about every 30 minutes and had pronounced anxieties, insomnia and depression....I had never suffered from depression before. I also started to experience heart flutters and eczema in my ears.

In desperation I began searching (pre-Google days) for clues in some home medical dictionaries. I came across gout and one of the recommendations for managing this affliction was to cut out all rich and fatty food. Although I knew I did not have gout I thought my problem may have been related, particularly with my swollen ankles which by then had turned a rather nasty brown colour. I decided to experiment and immediately cut out cheese, butter, mayonnaise, oils and fatty meats to achieve a very low fat diet.

Within two days I was feeling much better and over the course of the next month I continued with my experiment and found that within about 24 hours of starting on a higher fat diet again my symptoms would begin to return. Over the next four years and after spending a lot of money on private consultations with no diagnosis being given my doctor eventually referred me to the Royal National Hospital for Rheumatic Diseases in Bath. The consultant diagnosed Poly-Reactive Arthritis. I told him about my very low fat diet (under 20 grams a day) which I had been trying. He said if that worked for me I should keep doing it. Subsequently I developed lactose intolerance. Symptoms from this appear two hours after eating any dairy but I have not found any known connection between this and Reactive Arthritis. I also developed problems in my lower back and X-Rays confirmed that this was caused by arthritis. I am unable to lift even fairly light weights and cannot operate a vacuum cleaner without getting severe back pains for a couple of days.

The diagnosis of Reactive Arthritis was six years ago and if I keep to my very low fat diet I am able to lead an almost normal life. However, I now find that in the past year I have had an increasing amount of urological problems such as cystitis and what were though to be bladder infections, although all the urine tests proved negative. I have also been investigated for possible kidney stones but again this has been negative although on one occasion there was blood in the sample. I have found out in the past few days through Google that symptoms like this are often associated with Reactive Arthritis and called Interstitial Cystitis.

Recently I found the web site for the Arthritis Research Campaign which has a very good information booklet on Reactive Arthritis and in an answer to my questions advised me that cutting down on fat can make a difference in most types of arthritis including inflammatory arthritis, particularly saturated fats which can increase pain and inflammation in the body.

They directed me to their information booklet Diet and Arthritis on their web site at www.arc.org.uk. In this publication they recommend concentrating on oils such as olive oil, walnut oil and oil from fatty fish. I thought I would again experiment and only eat the fats they recommended even though I felt sure that too many olives and olive oil dressing would cause a reaction. Twenty four hours after crossing my 20 gram threshold my symptoms reappeared then slowly subsided after I returned to my strict diet.

In all of my research I have not come across any suggestion for treatment of Reactive Arthritis by a low fat diet. I only know that it has worked for me so far.

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Sulfasalazine :: Works For Reactive Arthritis ?

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I've been taking Sulfasalazine for a couple of months now, my hair thinning, I've put on weight (about 8 lbs) I feel really down a lot of the time and my moods can swing, I'm normally such a cheery person

Anyone else had/got reactive arthritis and taken Sulf to treat it? i had most pain/swelling in my knee's.

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Reactive Arthritis :: How Many Joints Are Involved ?

How my joints are left after having reactive arthritis

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Post Streptococcal Reactive Arthritis - Frequent Attacks

I'm a 35 year old woman and last year I was diagnosed with Post Streptococcal Reactive Arthritis. I also have ME/CFS which was diagnosed when I was 15 years old.

In July I had sore throat that lasted for 3 weeks and wasn't getting any better so I visited my GP. She thought it was a virus but did a swab anyway. Over the next few days I noticed weakness, pain and swelling in my hands and knees, worse on the right side of my body. The pain got so severe I could not stand or use my hands. I went back to the GP and was told my swab tested positive for strep. I was given a course of penicillin and told to take ibuprofen and co-codamol for the pain. I was also given omeprazole to protect my stomach as I had gastritis a few years ago.

The pain continued for 2 weeks, I had another course of antibiotics but it wasn't helping so I was admitted to hospital where I was diagnosed with Post Streptococcal Reactive Arthritis. I was given stronger antibiotics and painkillers and a steroid injection (kenalog) and discharged. I gradually improved over the next few weeks but then in October I got a chest infection and another throat infection. 3 weeks later the Reactive Arthritis flared up again.

I was referred to a rheumatologist who examined me and said there was nothing wrong with my joints. He did lots of blood tests but they all came back negative except for a borderline strep count. I was discharged back to my GP as the rheumatologist couldn't help me because my arthritis was caused by infections. He said I needed investigations to find out why I was getting so many strep infections. I went to see my GP but she said there is nothing they can do. She said there is nothing wrong with my immune system because my blood tests are normal.

I had another throat infection in January and another in March, both of which lead to reactive arthritis flare ups. I am very fed up of being ill and in pain all the time. The doctors don't seem to be taking me seriously at all and the only treatment I've been given is codeine and paracetamol for the pain.

I would very much appreciate any help or advice. Surely the medical profession can do more than just give me painkillers?

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Reactive Arthritis Caused Prostatitis And Vice Versa?

I notice lot of people talk about treating arthritis but does anyone here have prostatitis due to reactive arthritis or arthritis caused by prostatitis?

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I do a lot of swimming and can't find a decent remedy or barrier for eczema. To be honest I control it pretty well but it flares up to the extent that it is incredibly uncomfortable and it is always the next day after I have been swimming. I then end up taking an antihistamine which makes me drowsy and then has an affect on my training (doing an ironman) for the days that follow. Can anyone recommend anything?

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Knee Problems From Cycling?

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Atrial Fibrillation :: Sleep Issues And Cycling

I started with a really fast and irregular pulse and heartbeat last Wednesday night and took myself off to A&E. I spent the night wired up to a monitor and had a saline drip with some other medication to try to bring down the rapid heart rate. During the night I had an injection of a warfarin type medicine (claxon?) and beta blockers. The following day I was taken to the Coronary Care unit where I was given a further injection and more beta blockers, bisoprolol fumarate. I met with the cardiologist she explained that I had Atrial Fibrillation, although my heart rate had come down the irregular beat was still there. Further treatment a couple of months down the line were explained to me but now, one week after discharge I have a few questions I would like to ask fellow sufferers who have permanent atrial fibrillation. Oh, I am currently on 5mg of bisoprolol fumarate and 3 mg Warfarin.

1. Do people have any tips for getting off to sleep, I can't seem to settle at all with a banging heart even though my pulse is sort of normal, (with a few missing beats).

2. I have just come back from a cycling holiday and usually walk about 4 miles a day, after a very slow walk today I am exhausted, any tips on getting back to normal.

3. I saw my own GP yesterday and he said that I should get back to 'normal' cycling etc, I did ask if I could have a glass of wine or beer, he said that's fine, however I have read that this  can make the AF worse. Any thoughts?

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Lichen Sclerosus :: Cycling With Vulva Issues?

In a bid to get fitter, I bought a mountain bike, since I did used to love cycling. I guess I did not think it through and realized so, once I sat on the very hard seat. 

Any tips for people who are cycling currently with vulva issues? I have seen some saddles with what I can only call 'slits' in, which seems like a good solution, since the pressure on the vulva area would be less?

I also read that wicking away material is good and I to measure one's sitting bones. (Not an easy task). 

So, question. Any other ladies managing to cycle with LS on the vulva? I also suffer vestibulitis, vulvodynia. However, not to be thwarted (!) I am happy to look at a new saddle. It would appear one with a cushy part for the sitting bones and a slit for the vulva to relieve pressure is the way to go?  Any tips, any experiences, that may help would be much appreciated. Or, names of seats (that are not too expensive if possible). 

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Arthritis :: Mild Arthritis - Skin Feels Sore

After MRI my diagnosis was "Lots of mileage left, another 10 years, at least!" (I am 75)! Good to hear but still have to be careful going DOWN stairs! Not too bad going up! Some pain now and again. BUT I sometimes get a strange feeling on upper left thigh, (the worst knee), as if it is wet but when I touch the skin it is totally dry! Happens after I have been standing for a couple of hours.Also, sometimes the skin feels sore, but there is no evidence to show. Has anyone had similar feelings?.

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Hepatitis :: I Have A Reactive HBsAg

I am a fresh graduate and I was looking for a job then found one, I was hired and before I could start they wanted to get my medical result first. They told me I won't be able to get the job anymore since my result in HBsAg was reactive. In the medical it says "3516.26 S/CO; The Cut-Off value reported for this assay cannot be correlated to an end-point titer; rechecked and verified." Is my Hep B chronic? And can I still get a job even though I am now a carrier of this disease? I am really depressed now it's like I've wasted 4 years of studying

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Idiopathic Reactive Hypoglycemia

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Im 20 years old and am currently taking ortho tri cyclen, and occasionally take vyvanse and ambien.

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Recently I read somewhere that it can be caused by vitamin D deficiency. Well that would make sense timing wise, I live in Scotland (no sun here) and I stopped sun holidays 3 years ago due to drop in income.

I was excited by this discovery but well 8 days in (5000iu) and no improvement. I know it probably takes a lot longer and I'm still going, but I hope it's not just a red herring.

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