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[...] Resources: Arthritis Message Boards/Online Support Groups (fightingfatigue.org) [...]
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[...] Fighting Fatigue CFS & Fibromyalgia Blog Carnival #9 (fightingfatigue.org) [...]
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[...] CFS can be a difficult illness to diagnose because the severity of symptoms fluctuates among each patient. The only way to diagnose CFS is through eliminating all other possible illnesses and by following the CDC diagnostic criteria for CFS. [...]
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[...] June News From the CFIDS Association (fightingfatigue.org) [...]
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[...] had my quarterly check-up yesterday with my family doctor and I told her about my instance of brown urine I experienced last month and she didn’t write it off immediately as IC symptoms as the [...]
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[...] Fibromyalgia & IBS News Around the Web : FightingFatigue.org [...]
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[...] Resources: Arthritis Websites & Blogs (fightingfatigue.org) [...]
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[...] Why Weight Gain Is An Issue for Fibromyalgia Patients … By Sandy Robinson Hypoglycemia. Hypoglycemia, or low blood sugar, is also common with FM. According to Dr. Pellegrino: Increased sensitivity to insulin will result in too much glucose being removed from the blood stream and pushed into the muscle. … FightingFatigue.org – http://www.fightingfatigue.org/ [...]
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[...] cystitis that really got my attention. It included a link to a post on her site, Fighting Fatigue: Urine Test Developed To Diagnose Interstitial Cystitis. On July 24th, the Interstitial Cystitis Association (ICA) reported regarding the development of a [...]
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[...] ME/CFS Research Abstracts from ProHealth : FightingFatigue.org By Sandy Robinson Red yeast rice is an herbal supplement that decreases low-density lipoprotein (LDL) cholesterol level. ["Bad" cholesterol.] Clinical Case Report: Ultrastructural Evidence of Skeletal Muscle Mitochondrial Dysfunction in Patients With … FightingFatigue.org – http://www.fightingfatigue.org/ [...]
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[...] Original post Share and Enjoy: [...]
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[...] Urine Test Developed To Diagnose Interstitial Cystitis [...]
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[...] Back in May, I posted on Fighting Fatigue about Dr. De Meirleir’s discovery of a diagnostic test for ME/CFS. For more information, please read my post Breaking News: ME/CFS Cause & Diagnostic Test Found According to Researchers. [...]
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[...] bag while they get together the needed materials (you can read Ampligen from a patients perspective here). I know its summer time, but seriously the guys down at the FDA need to pull it together and let [...]
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[...] Personality Changes with ME/CFS (fightingfatigue.org) [...]
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[...] today I will start by stating… I’m not lazy–I’m sick. (Thank you to the author of this article.) “How many times over the years have you been accused of being lazy since [...]
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[...] month I wrote about how Celiac Disease can be misdiagnosed as ME/CFS and why this happens. Just last week I found out that a friend of mine who has been suffering [...]
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[...] SheSource: Fighting Fatigue RSS Feed [...]
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[...] The Fibromyalgia Cookbook : FightingFatigue.org – I just finished going through The Fibromyalgia Cookbook and found some interesting information on what foods should be avoided for Fibromyalgia patients. The author of The Fibromyalgia Cookbook, Shelley Ann Smith, suffers from … [...]
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[...] and I have found the book to be rather fascinating. I wrote recently on Fighting Fatigue about how Celiac Disease can be misdiagnosed as ME/CFS but I never realized that Celiac Disease is only one type of gluten intolerance. You don’t [...]
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Feeling your pain with the ears, sinuses, etc. It’s been constant for months. Just got diagnosed with menopause. I’m thinking Fibro too.
Just wanted you to know that you’re not suffering alone.
I was just diagnosed with a vitamin D deficiency on Monday. My level was 14.5, pretty low. I walk an hour outside everyday but use sunscreen and I also take a caltrate with D and a one a day with 400IUs of D. Now he has me on 50000iu once a week for 8 weeks. He said if I can go south in the dead of winter, that would be the best thing…yah. Hubby would love to, maybe visit Mickey Mouse. My doc said we can build up a reserve but it won’t take you thru the whole winter so keep taking supplements. The best ones to take are D3 and take about 2000IU a day for optimum protection without overdosing. This has been a hassle getting diagnosed but I think it answers lots of questions of how I’ve been feeling the past year. Hope the supplements work.
My doctor has me taking 500,000 units or mgs. of Vit. D once a week. Is there anything I should be concerned about by taking this high of a dose?