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

13 Replies

  • Posted

    Hi Please go and see a doctor its taken me four months from my first gp visit to get a diagnoses of RA it really does sound like you need to have blood tests. Keep perservering till you get an answer too. 
    • Posted

      Thank you very much!! I've been debating I guess telling myself all the reasons why I wouldn't have it but I will ask my doctor specifically for the blood test!! Thank you for your time!!
  • Posted

    I'm new to ra.  I first noticed my thumb on my right hand was sore.  Unusually when I was blow drying my hair. I started having psin in my right hand and then it went to above my knees on both sides.  I couldn't get off the couch without difficulty and sometimes had to roll myself off because I couldn't use my hand to brace  myself.  I went to the doctor and asked him if there was a blood test that would show why this was happening.  He said "you mean RA?"  He looked at my hands and said I didn't have any nodules so he just put me on arthritis medicine which didn't help.  

    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!

     

  • Posted

    Please go to the doctors it sounds very much how my r.a started keep on at doctors for bloods I hope that it's not the case for you good luck x
    • Posted

      Thank you Tina!! I hope it's not the case as well. I'm just trying to get someone else's POV!! Thank you for your time!!!
  • Posted

    Hi Brittany sounds like Ra, but you'll need to go through the system, which will take a while. Don't worry though their treatments are pretty good for this autoimmune disease, although there is no cure there is a good chance of remission. Ask to be referred to an early arthritis clinic asap regardless of your blood test results. The blood tests can be negative, but you still have it, this happened to me. I paid for a private consultation in the end. I'm 28 so I know what it's like, good luck to you. I've had to wait 6 months to get to the early arthritis clinic! If treated early the prognosis is better oftentimes.
  • Posted

    Hi, your articulation of your symptoms is so well described. It sounds very much like you have full blown RA, rather than early RA, and as if you are in a painful flare up. While in this highly inflammatory state, the damage is so very high on your body and joints and is irreversible. Before more damage and pain incurr, please go for medical care so you can be treated fir this, being prescribéd a prednisone pak to get your inflammation down and hopefully managed well. I found many things were triggering this state of the disease, which evolved around malasorbing of nutrients in my colon, caused by my eating gluten, high sugars, dairy, soy, and other highly inflammatory or allergery sensitive foods..as well as high stress within myself and/or environment, less than 10 hrs of nightly sleep and an improper balance of vitamins, nutrient and minerals to which I had to supplement. I found that I strongly needed calcium( with 2000 mg D3) and magnesium glycinate, taken in a 2:1 ratio and a good multi vitamin along with fish oil capsules (do not use unscented). I also found most of the RA medications prescribed (methotrexate, biologic injections, sulfa drugs) were not effective for me and because they cause immune systems to be compromised, triggered infections, and kept me in consistant flares, such as you are describing. An anti inflammatory is highly needed for you and I finally ended up with plaquenil which takes some time getting into my system, but did not trigger or cause underlyinging infections. What now causes the high inflammatory states for me are the things I've shared above, rather than a painful combination of the contributing factors with the RA treatment that just made the disease worse and unmanaged. I would make an appt as soon as possible and then be very proactive in what works for you personally.
    • Posted

      I'm sorry I didn't read your post before I updated! Thank you so much for all of your ideas I will take def take them! Thank you very much for you time!!!
  • Posted

    I also need to take prescribed Tramadol for the pain, caused by the damage that has been done to my body caused by unmanaged and improper treatment of my high inflammation rates. The calcium with D and magnesium glycinate ratio of 2:1 took away all of the fibromyalga all over pain, which I've been able to manage for 4+ years due to this.
    • Posted

      Your description of your experience seems like I can def relate to yours. The triggers you describe are all areas that I have been lacking lately. I need someone that I can relate to through this bc my family doesn't seem to understand. If you have extra time my e-mail address is _________. Its always good to have people to connect with while dealing with this terrible disease. Looking back I feel I have been dealing with this my whole life even in childhood and that may be a reason I've dismissed these symptoms.

      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

  • Posted

    Hello everyone thank you for your encouragement to see a doctor!! I don't have insurance at the moment I'm in the process of filing for some so I went to an immediate care facility. The doctor there did diagnose me with RA without any blood test just from the damage I already have to my pinky and ring fingers and same on my toes! I was very shocked and scared to hear that. I know at 27 the prognosis isn't good. Does anyone have any ideas for lifestyle changes such as diet etc that I could make until my insurance goes into effect? Thank you all so much for your encouragement to see a doctor!!
    • Posted

      Hi Brittany,

      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

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