Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum. ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
jmbirds Female, 43 years gloversville - NY Member since Jun 2008
Mood: jmbirds stressing
Thanks for your suggestions. I've been to a chiropractor for 3 months. My insurance has paid for all they are going to pay for that treatment. I am also low in Vit. D and am on 100,000 IU/week. I'm on my third month of that.
Mood: PlateletGal zapping mycoplasmas ! Journal Entry: "
The feel good story of the day:
Woma..." [Read]
, Jul 09, 2008 02:14PM
To: All
Add me to the list of people with either CFSChronic fatigue syndrome or fibro who have a positive ANA titer. Mine is also very high ---- 1:640 (speckled pattern).
The high ANA pattern is probably due to the Raynard's, although 29% of fibromyalgia patients do have a positive ANA titer (normally not that high).
You say you have a red rash on your cheeks... have your physicians ruled out lupus ?
http://www.labtestsonline.org/understanding/analytes/ana/test.html
God bless,
KaraJo
I have done plenty of research on the subject. The only meds I'm on is Armour Thyroid and Vit. D. I do takes tons of vitamins and herbs trying to get well. But I've been sick with them and sicker without them. Trust me, I'm almost dead w/o them.
Thanks for the internet site. I'll check it out!!
God bless,
KaraJo
What does Pomegranet juice do for you? I am really into natural supplements, but whatever I have has kicked me good. I've been sick for over a year. First it was my gallbladder that quit working, then they discovered hydronephrosis and and obstruction in my ureter. Then the elevated ANA along with all of these crazy symptoms.
What was your ANA level, and what was the pattern?
KaraJo
Ever since I got CFS my ANA was always positive. It used to always be either 160 or 320 and this year has went to 640.
The Rheumatologist thinks my rash is malar but don't have enough of lupus symptoms. He said I do have a connective tissue disease. My body attacks my white count so it's always low.
Postie
Postie, 10 years is a long time to have CFS. I've read that CFS usually last only 5 years.
PlatletGal, are you satified with the CFS diagnosis? Do you think you really have lupus instead?
so i would again say those with CFS or FM JUMP on the VIT D and ask for synthyroid trial and after 3 days of synthryoid 50 mcg and vit D i almost feel normal now i would try taking digestive enzymes walmart has them look for amelyase lipase and protease these enzymes are part of our filtering system liver gallbladder spleen pancreasis now pomegranit juice is another big antioxident can't hurt to try if your organs are not making the right amount of enzymes aka thyroid we need a booster to balance out the levels now i was just reading on webmed or medicinenet.com lots of hypo thyroid things and so take a peek can't hurt