IDES Timeline

Does anyone know what day of the week San Diego gets findings in from DC or what day they usually let people know they’re stuff is in?
 
Does anyone know what day of the week San Diego gets findings in from DC or what day they usually let people know they’re stuff is in?
I’m not to sure if it matters based off of the area. But should be around every Tuesday. Some days it’s later in the week and sometimes the PEB doesn’t get one done and skips a week.
 
Just wondering, does anyone know roughly the turn around from QA to getting your findings? Mine has been at QA for about a week. Just want to know any rough estimates as my PEBLO is not of much help and almost seems annoyed I keep asking about my case
 
Just wondering, does anyone know roughly the turn around from QA to getting your findings? Mine has been at QA for about a week. Just want to know any rough estimates as my PEBLO is not of much help and almost seems annoyed I keep asking about my case
Mine was at QA for 23 days to when I got my findings.
 
Just wondering, does anyone know roughly the turn around from QA to getting your findings? Mine has been at QA for about a week. Just want to know any rough estimates as my PEBLO is not of much help and almost seems annoyed I keep asking about my case
Currently I'm at day 19 of QA
 
Does anyone know what day of the week San Diego gets findings in from DC or what day they usually let people know they’re stuff is in?
Im in San Diego also, I heard its normally on Tuesdays but heres to the long wait. Hopefully youll get your results soon. Im at 156 days
 
a little update:
submittted 09sep21
mo since 05oct21
Found unfit today, peblo said should be receiving official call in about 3 weeks (won’t cross my fingers) but there is hope!!
 
Ohhh got it. Mine is fibro too and I’m waiting on my percentage. The way I understand it the rate should be 40% based on not cured by therapy (no one is cured for fibro from therapy) but my assumption is they will give me 20% also…
Soo.. I actually know why I got 20. The va dr asked me what my symptoms of fibro are. I started naming them, and he stopped me and said, yeah but how do you know those are because of fibro? I was like uh idk. So the DOD says they’re related and under the fibro umbrella. VA says they aren’t.. va had to be challenged within a certain amount of days and my doctor said she was going on leave in a few days and had scheduled c-sections in the days prior. So I’m getting out because I have a great job in my hometown that I’ve been interviewed a few times for…
 
A higher evaluation of 40 percent is not warranted for fibromyalgia unless the evidence shows:
• Widespread musculoskeletal pain and tender points, with or without associated fatigue, sleep
disturbance, stiffness, paresthesias, headache, irritable bowel symptoms, depression, anxiety, or
Raynaud's-like symptoms that are constant, or nearly so, and refractory to therapy.
 
A higher evaluation of 40 percent is not warranted for fibromyalgia unless the evidence shows:
• Widespread musculoskeletal pain and tender points, with or without associated fatigue, sleep
disturbance, stiffness, paresthesias, headache, irritable bowel symptoms, depression, anxiety, or
Raynaud's-like symptoms that are constant, or nearly so, and refractory to therapy.
The doctor for my DBQ decided not to listen to my answers for Fibro and didn’t check refractory to therapy, didn’t conduct tender point checks, and didn’t check box for constant pain. Having my PCM write up a supporting statement so I can upload to VA.
 
The doctor for my DBQ decided not to listen to my answers for Fibro and didn’t check refractory to therapy, didn’t conduct tender point checks, and didn’t check box for constant pain. Having my PCM write up a supporting statement so I can upload to VA.
Yeah it might help it. It’s just crazy to me that one of my symptoms of fibromyalgia could be rated 70 and yet my overall fibro is only 20 when all my symptoms are clearly because of it
 
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