How many people with PA here feel pretty good? | Arthritis Information

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I'm another newbie to the forum.  I was diagnosed with PA less than a week ago.  I still need to meet with the Rhumatoid specialist to verify the diagnosis. My feet began to hurt 2 months ago and it got to the point where I was having a hard time walking at all.  I'm 30 years old, male, and I've never had any major medical problems in my life until the last few months.  To be honest with everyone, coming on the forum has been kind of scary.  Does anyone have PA and still live, walk, and function as well as they did before PA?  My mother was the first to get online to do research on PA, and it left her with heavy concerns for my well being.  One of her biggest concerns was that PA seemed to affect so many different joints in different people.  She's afraid it's going to move to other parts of my body.  I don't generally get sick and that's how it's been all of my life.  I'm trying to look at this the same way, but it's difficult. Can you have PA and have it treated effectively enough to live a normal life without daily pain? Yes you can be normal you just might have to adjust what normal is to you. I'm sure you will have a muchdifferent outlook once you start your meds. Will you be able to do everything you did before? Maybe, or maybe you will like the majority of us and modify those things. Don't be discouraged you will be okay, and hopefully better than okay. I'm 31 so I totally get where you atd coming from. If you need to vent I'm here. Actually I usually hang out in RA forum, lots more conversation. You will find all the support you want and need here. Take care. Thanks for the response.  It sounds like I will have a better idea of what you mean after I start taking meds.  My biggest frustration has been not being able to walk very well, if at all sometimes.  If I can walk enough to exercise without all of the pain, I'll be happy.  I think I read another post by someone that said when you have PA you develop a very close relationship with pain. That made a lot of sense to me.  I'm just hoping that there are a lot of people out there with PA that live what they consider to be a normal life.   Hi Shade and welcome to the forum.  I was diagnosed 4 years ago.  I also have RA and the disease can overlap.  Once you start meds you'll begin to feel much better.  The pain will be less.  Yes, you can achieve a level of normal.  Don't be too fearful and don't let denial take control of your thoughts about this disease.  You need to be realistic, start the meds that are prescribed and do as much as possible to return your body to it's previous normal.  It's not an easy journey but it's possible.  LindyHi Shade.  This is my first post on here, but I just had to reply to you.  My husband is 38 years old.  He was diagnosed with PA 2 yrs. ago.  He is extremely active:  mountain biking, hiking, surfing, running, climbing; so the initial pain and the diagnosis were terribly hard for him.  He has been on Humira for a year and is back doing all the things he loves.   Along with the Humira he takes glucosamine and condroitin, fish oil capsules and a couple of other homeopathic joint treatments.  He tries to keep his stress under control with meditation, yoga and massage, and he exercises religiously at least twice a day.  He also gets acupuncture treatments when he has severe pain in his wrists, ankles and knees.  In addition, we cut out gluten and artificial dyes, flavors and preservatives from our diets.  All of these things have helped, and he is back to leading a completely normal life.  On occasion, he does have some joint pain in the morning, but after he gets up and goes for a run, he's right as rain.   We recently went on vacation, backpacking for a week through the rain forest and then a week of surfing.  He was completely fine, with no pain or stiffness.

You can live a normal life with PA!  I think the trick is to find out what works for you and go with it.  My husband has been through several doctors, tried several medications, and really worked on diet and stress issues.  Good luck to you.
I really appreciate the responses. It's also great to hear the stories about people that are active and have PA.  It's been a while since I was here on the forum.  Things are considerably better than they were at the time of my first post. I've been on Methyltrexate for about 4 months now.  I also take Celebrex daily and Prednisone on the rough days,  Fortunately I haven't had a lot of rough days lately which means the treatment is working.  The time between my diagnoses and treatment was trying.  I couldn't walk and I think that really scared me, and it made the disease real.  I'm still trying to grip the fact that this is something I will deal with for my entire life.  That's a difficult pill to swallow, but I guess you take it one day at a time.   Hey, Shade,

 
I was diagnosed 15 years ago. Currently I'm in flare mode, but it seems to be winding down. For the most part I have a normal life. I do a lot of sailing and if that ever had to stop I'd wilt. Admittedly, I can't run anymore, but I walk 1.7 miles in 25 minutes [when not in flare mode]. Not bad for an old lady.
 
The key is early, aggressive treatment, a great rheumatologist, and learning how to pace yourself. I'm on Methotrexate and Celebrex [can't take the biologics] and I've learned how to be an expert at time management and pacing myself.
 
I'm glad to hear the rough days are few. And you're right - it's the fear that comes from not knowing exactly how your life will be impacted by the disease that makes it scarier than it is. Yes, you'll have to deal with it the rest of your life, but I'm confident that more and more good treatments will soon be coming from the research community.
 
By the way, you didn't mention taking folic acid. You need to take that when you take MTX. Depending on your weight 1-2 mg per day will do. Call your RD and get a prescription - don't use the OTC stuff.
 
I think we all learn to really appreciate the good days. Good luck!
Shade,
 
I'm curious...... My PsA began after a strep infection. Ironically, my brother caught the same strep infection and, unbeknownst to me until months and months later, he was diagnosed with PsA, too.
 
Do you know what triggered your PsA?
Im curently coming off of prednisone and the lower the dose the worse i feel but i wanted to try a few things before the methotrexate. But i will go back in a couple of days and more then likely be put on metho. My knees realy hurt alot but lately my right anklle has been hurting in the morning better as days go on also my elbos have hurt a few times the last couple of days and they have never hurt me. So i will tell doc this and he wants me on metho so now im ready. Mobic didnt work and prednisone helped a two pills aday. So i hope i teact well to the metho. I feel good as long as i dont do to much my prblems seem to be more prevelant with more activity. some days though it doesnt mater what i do it just hurts.it started whn i turned 29 !  My left knee then my feet than my hands and wrists and now left shoulder.  I have lost the use of my hands.  Drugs like enbrel stop it!  But it's not long term, maybe 4 years of treatment barring no side effects.  I have tried many treatments, now I have run out.  trying  drugs I've previously tried.  I am not happy!  The last 17 years have been hard, and now it's beatn me up hard.  you have to try to keep movin no matter what.  try aleve while your waitn to see a doc.Alive and advil were doing nothing for me. Even at max dose anternating between the two. That and the fact wife was getting upset that i was groaning in my sleep. So now im on tramadol and metho hope it getts the pain down. Thanks for the advise. I took a bath and used my hand to run warm water over knee and that hurt  not on the skin but deep in the knee not a severe pain but pain very weird. I hope all find some pain relief
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