Extreme Fatigue
| 3 forum posts | 0 articles | 0 doctors |
Coping with Fatigue
by engel
In Lupus Support Forums > General & Support
"From all the symptoms, I find the hardest to cope with, and the most debilitating, the extreme fatigue. It gets so bad at times that I have to lie down, whenever time of day, wherever I am and whatever I'm doing. It's invisible, I don't even get pale or anything, and I know that sometimes people think I'm crazy, lazy, spoiled or all of the above. I want so much to be able to do stuff, to be ac"
In Lupus Support Forums > General & Support
"From all the symptoms, I find the hardest to cope with, and the most debilitating, the extreme fatigue. It gets so bad at times that I have to lie down, whenever time of day, wherever I am and whatever I'm doing. It's invisible, I don't even get pale or anything, and I know that sometimes people think I'm crazy, lazy, spoiled or all of the above. I want so much to be able to do stuff, to be ac"
Related Discussions:
EXTREME fatigue! posted in Fibromyalgia Support Group
Help with Fatigue posted in Fibromyalgia Support Group
Help with Fatigue posted in Fibromyalgia Support Group
Doctors say - 'Everyone thinks it's Lyme'
by Aly
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have a question for you all:
Since 2/26/07 I have had constant headaches, joint pain/soreness, muscle soreness, and extreme fatigue. Doing anything makes me feel worse, and I've been trying to fight the pain and go to work, but I've called out more than I've been in - I haven't worked a full week or a full day since 2/26. My brain feels sluggish and I haven't had the best"
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have a question for you all:
Since 2/26/07 I have had constant headaches, joint pain/soreness, muscle soreness, and extreme fatigue. Doing anything makes me feel worse, and I've been trying to fight the pain and go to work, but I've called out more than I've been in - I haven't worked a full week or a full day since 2/26. My brain feels sluggish and I haven't had the best"
Related Discussions:
Joint pain and he... posted in Acromegaly Support Group
Anyone have joint... posted in Fibromyalgia Support Group
Anyone have joint... posted in Fibromyalgia Support Group
NDPH and joint pain?
by Aly
In NDPH Support Forums > General & Support
"Hello everyone. I'm new to the site, my name is Aly, and I finally found a doctor who has been seriously treating my headaches. He thinks it might be NDPH, but I won't be starting on any medication for it until my MRI results come back - first he's looking for blood clots in my brain.
My question is this: Have any of you experienced any joint pain/soreness? Or muscle soreness? My headac"
In NDPH Support Forums > General & Support
"Hello everyone. I'm new to the site, my name is Aly, and I finally found a doctor who has been seriously treating my headaches. He thinks it might be NDPH, but I won't be starting on any medication for it until my MRI results come back - first he's looking for blood clots in my brain.
My question is this: Have any of you experienced any joint pain/soreness? Or muscle soreness? My headac"
Related Discussions:
Anyone have joint... posted in Fibromyalgia Support Group
Joint pain and he... posted in Acromegaly Support Group
Joint pain and he... posted in Acromegaly Support Group