What is the disease RA

Is disease ‘RA’ is curable if so, the remidy?

http://answers.yahoo.com/question/index?qid=1006042402325

If you are referring to rheumatoid arthritis (RA) no it isn’t curable at this stage. It is a virus that attacks the immune system and causes joint inflammation and permanent damage to the joints. Currently Methatrexate (cancer drug) is bein…

Is there a connection between RA(the disease,not the medication t…?

http://en.allexperts.com/q/Rheumatology-including-Arthritis-986/index_15.htm

Jo-Ann, RA is an auto-immune disease that can effect not only joints but almost any organ in the …

CAN ANTI-CCP ANTIBODIES PREDICT SEVERITY OF DISEASE IN RA??

http://www.jrheum.com/subscribers/06/07/1216.html

Among those already with an established diagnosis of RA, anti-CCP positivity has been able to predict, in numerous studies, the severity of disease. RA patients with anti-CCP have more radiographic joint damage as compared to those without …

Related Questions Answered on Y!Answers

is disease ‘RA’ is curable if so, the remidy?

Q:

A: If you are referring to rheumatoid arthritis (RA) no it isn’t curable at this stage. It is a virus that attacks the immune system and causes joint inflammation and permanent damage to the joints. Currently Methatrexate (cancer drug) is being used by specialists to stave off the growth of RA. Apart from that, there is no cure. You can try Royal Jelly capsules and Glucosamine capsules for joint inflammation. I hope this helps – Kay.

Is anyone suffering advanced stage lyme disease and getting no help?

Q: I’ve been battling this for years, Gone to several doctors and suffered needlessly. Now I am going to a Lyme literate doctor snd hopefully start to feel better. Lyme is now considered to be the great mimicker of all diseases. RA, chronic fatigue amd ever MS are more often misdiagnosed. I have a lot of insight on this subject if snyone should need medical attentionhttp://www.lymeinfo.net/lymefiles.htmlGo to this link and you’ll be surprised at what you read. Hope this is helpfulI have been diagnoses with chronic fatigue and I have had many diagnostic tests…brain MRI, blone scans, MRI of my wrist and several blood test. The blood test for lyme did come back positive but most conventional doctors ignore false negative and even positive. I have cyst resistant lyme now so even antibiotics useless. It is very important that you see a lyme litterate physician. I am seeing a homeopath here in CT and he has been very helpful. the cure is a very long road but you have to be patient and in most cases, you will feel worse before feeling better. I have been fighting this for years so I have nothing to loose. Be your own advocate!I’d also like to add that I have spent thousands of dollars going through the revoling doors of several doctors and getting the same results. They can see things on films, scans, etc but no answers. One of the worst disasterous things I hear quite often is that people that are diagnosed with CFS are almost always sent to a shrink because these so called trained doctors can’t figure it out. That is a generic diagnosis when they can’t prove anything and still people suffer needlessly. It is said that lyme is the great immitator of several diseases. I hope that anyone out there that suffers with debilitating fatigue or any other symptons that have no explanation, seek help from a doctor that thinks outside the box. I am 49 now and am hoping I have a few years left in my life that is worth getting up for. Another excellent book to look into is:http://www.lymebook.com/It tells it all and give people the optiion to look at all treatments to consider. I really hope this helps all of you!

A: battling level 3 lyme myself. i got bit by two ticks last labor day and was diagnosed in december already at level 3. full involvement of joints, especially knees, to the point that i can no longer climb stairs and if i sit for a few minutes my knees hurt so bad standing up i just about cry. heart involvement with arrythmia- i have had coronary spasms for years so already have a cardiologist who is following closely for heart damage from the lyme. the worst is the brain involvement… i have always had a great memory and been very sharp and alert, but with this disease you just lose it. i can no longer concentrate and focus for more than a very few minutes, i get disoriented easily, i forget things and i simply can not process my thoughts any more in a coherent manner. i avoid driving any more than i absolutely have to because i find myself getting “lost” (disoriented) even on familiar stretches of road. i am on antibiotic treatment, but there has been no improvememt and a stronger antibiotic is going to be tried in the hopes of getting a remission. i never knew lyme disease was like this and now i try and educate people so others know just how devastating this disease is.

How do you deal with the extreme fatigue that goes along with autoimmune diseases like lupus and RA?

Q: It’s getting kinda old. I just want some energy and caffiene isn’t giving me its usual kick.

A: In the long run, caffeine will only make the fatigue worse as you stress your body by putting it through a roller coaster of ups and downs. Learn to conserve your energy. Instead of washing a whole sink full of dishes, wash dishes for 5 minutes and then rest for 5 or 10. Instead of cleaning a whole room, clean one corner then rest. Pushing yourself makes the fatigue worse in the long run. Break up tasks into smaller tasks and take frequent breaks.Rest when you are tired. This is hard to do if you are working, but when you are not at work you can do it. Lower your standards. You don’t have to be super person. You have an autoimmune disease that causes profound fatigue. If someone you loved had this disease, would expect THEM to soldier on? Love yourself as much as you love that person.Do not do for others what they are perfectly capable of doing for themselves. Remember no one is indispensable. You or I could fall of the face of the earth today and the world will keep on turning. Prioritize. What’s more important, making sure there are no dust bunnies under your furniture or having enough energy to spend time with your family and friends?Get some exercise everyday. I know, you have no energy and it hurts. Can you take a 5 minute walk each day? If you can’t go out, can you walk in place indoord for 5 minutes? Exercise reduces pain and fatigue. You have nothing to lose by trying. Maybe tomorrow you can do 6 minutes. Set reasonable goals that you know you can achieve.Avoid caffeine. In the long run it makes the fatigue worse and takes a toll on your heart, something people with inflammatory autoimmune disease don’t need since we are more prone to cardiovascular events.Eat a healthy and balanced diet, high in fresh or frozen fruits and veggies and low fat protein. Candy, cake, chips, pop tarts, honey buns, sugary cereal, etc. don’t give your body the elements that turn into long and sustained energy. They cause a spike in blood sugar follwed by a crash where you feel even worse.Laugh. Watch funny movies, read funny books. Laughter improves immune function. Do hobbies that give you pleasure but don’t require a huge output in energy. And always be gentle with yourself. You may not be able to change what has happened to you but you can change your reaction to it.