Autoimmune Diseases and Fatigue
Fatigue is probably intertwined with the definition of "illness", almost any illness, but with some conditions fatigue becomes ingrained into the afflicted person's being and is a feature of their daily life. Such is the case with the highest profile disorders, cancer and cardiovascular disease, but it is just as true with at least some autoimmune diseases. I have a long history of dealing with autoimmunity and the complaint that kept bringing me back to doctors persisting in finding out what was going on was the dogged lack of energy, vitality. I got guess after guess after guess and when I got the "answer" it was basically that fatigue was part of the deal with the autoimmune disease that I have, Sjogren's, as well as I'm sure many others. So what I'm asking here is if you experience it, fatigue, how has it impacted your life and how do you deal with it? Have you found anything that you are sure mitigates it?
In my case its exercise, rest, and a fairly regulary low dose, around 50 mgs (usual recommended dose 200 mg) of modafinil, which I don't take for Sjogren's but rather for "Excessive Daytime Sleepiness" linked to Obstructive Sleep Apnea. I accidentally found out that it mitigated my general weariness. I've read some solid studies that found that American Ginseng can help cancer-related fatigue but apparently it doesn't work for Sjogren's, for me at least. Since fatigue impacts a person's total life experience in all domains, any information that might lead to dampening or controlling it would be very helpful to a lot of folks I'm sure.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
If this what you mean there is a way out of it.
http://www.irondisorders.org/hemochromatosis
Hi @barb54, you may also wish to join this discussion "Interstitial Cystitis - I would like to connect with others" http://mayocl.in/2babJXN
Im 53-4 I cant even clean my house my fatigue is so intense I spend a lot of my time researching to beat fatique let u know if I find anything out Best to all Dee
Hows that work? I am badly fatiqued if you care to share ? Would be much appreciated thanks and Nothing to loose thanks good day Deena
I control my edema aka belly bloat with Tumeric Curcumin bioperine I was on paleo auto immune diet and set off the worst fatigue I have put some Gluten free carbs back in my diet I feel better just 1 serving a day gluten free pasta or a wrap I have auto immune PBS and a stone in pancreas for 5 years before they found residue from stone passing which put me at highest risk for pancreatic cancer. I been taking astragulus root seems to give me a little energy or is it the carbs .Checking out magnesium seems 80% of population is deficent and #1 supplement in Japan ! Watch your salt intake it you bloat and lemon water is vital to keeping our PH up! Acid and sugar create a happy cancer envioment!
I understand I am relentless when it comes to feeling better! Dont give up keep moving forward there is got to be something over looked? Feel better payers for your well being Deena
I so agree that it seems like you have to suffer a long time and go through several doctors and rounds of testing before you find a diagnosis. I was finally diagnosed with RA, fibromyalgia and Sojourn's syndrome after five years! I even went to special diagnostic hospitals. I have had these conditions for 10 years now - actually 15 since it took five to get any one who knew what was going on with me (all started around age 40). I am doing better. I have good and bad days, but more good. It took a long time to come to grips that I would never be as active or feel as healthy as I used to. I pray you find answers and relief soon. Don't give up! It does get better. Maybe not great, but better.
I agree. But you need to try to move and not succumb to the pain. I am not, and understand will not ever be, the same as I used to be before the downward spiral of my health. However, I know I could be so much worse. Took me a long time to learn how to pace myself. Move enough to help but not do too much to where I flare and hurt too much to move at all! You can feel better - never the same, but better. Walking or swimming is a must, though. You have to move - even though I know it is really, really hard at the beginning. And try your best to ignore "friends" and family who don't understand. Try giving them some literature to read about your chronic illnesses. If they still are difficult, I just wouldn't bother much with them any more. Forums like this are helpful because we have been there, done that (and that and that) and understand. Know you are not alone and there is hope. Just don't give up!
Thanks for site!
Take a vaca from your issues maybe a yoga or tai chi class massage therapy you need to destress music? Something calming you deserve to do it for your self