Help Please! Do I have early signs of RA?
Posted , 7 users are following.
Hello,
I am 27 yrs old and have always been in pretty good health. About six months ago I started to notice throughout my day I would feel as if I were running a fever and would be very fatigued. Over time it has gotten more frequent and about four months ago my feet started bothering me on my forefoot both feet. I have a separation between my 2nd and 3rd toe on both feet which I've been told comes from swelling.The bottom of my feet have what I think are nodules one small under my pinky toes at the base and big ones on my forefoot under almost every toe. I have an obvious curve in the 3rd 4th and pinky toes. My toes look like the are going to be "hammer toes" and I have a callus on my 3rd and 4th tip toes. My hands and feet started swelling in the joints. My index finger on my right side has felt sprained for quiet some time. I noticed that even before the fatigue and fever and is getting worse. I also have what I think are nodules on my middle finger, thumbs, base of my pinky and on my palm at the base of my ring finger. I am also swollen around the base of each finger and thumb. Some days I have hardly any swelling but I still have the pain that feels like it moves from joint to joint and also my calve muscles have been bothering me. I have stiffness in the morning to the point I have caught myself shuffling when I get out of bed. My shoulder and hip joints are sore also. My grandmother has RA and she has mentioned my whole life things about my fingers. Can anyone tell me if these are significant signs or if I need to wait on seeing a doctor? Thank you so much for your time!!!!
2 likes, 13 replies
helen263490 brittany19819
Posted
brittany19819 helen263490
Posted
Buckeyes brittany19819
Posted
Wih all of your symptoms, fever, swelling, nodules, fatigue,I would suspect ra but it could also be some other auto immune disease. I only have been reading about ra simce that's what I have. It took me a year to find out what was wrong with me, even going to ortho docs that told me I had minor carpal tunnel and tendonitis. Eventually I went to a nurse practitioner who finally did blood work and that's when I found out!
when you go make sure they do blood work and Check for ra! If I hadn't' pursued it I still wouldn't know!
good luck and please post and let us know what you find out!
brittany19819 Buckeyes
Posted
tina41716 brittany19819
Posted
brittany19819 tina41716
Posted
chris80623 brittany19819
Posted
cheria brittany19819
Posted
brittany19819 cheria
Posted
cheria brittany19819
Posted
brittany19819 cheria
Posted
Emis Moderator comment: I have removed the email address as we do not publish these in the forums. If users wish to exchange contact details please use the Private Message service.
http://patient.uservoice.com/knowledgebase/articles/398331-private-messages
brittany19819
Posted
raralady brittany19819
Posted
i was diagnosed with RA around 18 months ago. By the time I got the diagnosis I'd been in the grips of a severe flare-up for several months which entailed terrible joint pain and terrible fatigue. Everyone's different but I really didn't want to take immune suppressing drugs so I went on a quest to find alternatives. I can only tell you about my own experience but it's worked for me.
I take a drug call Low-Dose-Naltrexone. It works by stimulating your body to produce hormones to help with the pain and swelling and there are no nasty side effects.
I have stuck to a gluten-free, grain-free, dairy-free, legume-free and deadly-nightshade-vegetable-free diet. All of these foods are inflammatory. I eat high protein, low carb, low sugar, high fat (mainly from nuts and coconut oil) and fermented foods such as sauerkraut to heal the gut.
I take omega 3 fats, magnesium, msm, glutamine, probiotics, digestive enzymes and curcumin.
Sounds like a lot but I'm well now, and it feels like a miracle.
I exercise if I can but not if it hurts. Tai chi is great for me and i use a mini trampoline every day which is easy on the joints.
It's not easy but there are alternatives to nasty drugs if you want them. Best way is to work with a Functional Practitioner or Psycho-nuero-immunologist if you can. They can do tests and make the best treatment for you as we're all different.
I wish you the best of luck and strength