Guest guest Posted November 2, 2000 Report Share Posted November 2, 2000 Dear ; You asked us: " Those of you that were turned down or those that got it, do you mind my asking what your age was at that time? " I applied in 1994 for SS disability, due to the fact that surgery brought on my FM, but at the time I thought it was my recovery that was giving me the problems not FM. I was turned down and just left it at that. In 1998, I reapplied because I was not " recovered " and was then dx with FM for all my pains and problems of " Fibro Fog " and all the lovely other symptoms we have. I was lucky because in my first application I did not count the time before the surgery as I was disabled (I was " out " of it, and couldn't function due to needing surgery) so they allowed me to add that time and reapply with " new " evidence. I was turned down the first time again, but stuck with it. I finally won the right to be called Disabled and was awarded retroactive money from when I first applied to SS. But I needed a lawyer and went to court in front of a judge. That was in 1998, two years ago. I am now 33. I still wish I could work, and feel bad at times that I can't work, but I need to cope with that and that is hard. One important suggestion that my lawyer told me and that I want to pass on is, when I went to court she told me not to make it sound better than it is. Wear your hair the way you always wear your hair, don't get all " dressed up " . If you have trouble doing things like hair and makeup then don't do it good for the day in court. Show you as you are normally when you go to court. Also, many people feel embarrassed and will not feel good if they really tell some people how it really is, and they can't admit that they can't do much. We should, cause it is bad. I remember being asked to tell about my normal day routine. Well, when I told the judge I felt like saying wow I don't do much what horror, but I told the truth. I think that that is important, don't feel embarrassed and feel you need to make yourself look better or say you can do more than you really can. It will not give the court a true image of yourself if you make it look better than it is. I hope all that made sense and that it might help someone. Take care Janice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 2000 Report Share Posted November 2, 2000 I was turned down the first time at 46....I also stand to get my late husband's benefits...if I survive the hassle...I can't wait the years and retire....I can't work now...today I think I may have to return to meds as I am burning all over....my pain tolerance is quite good but when the pain gates start to go I get a burning sensation...late husband did hypnosis and taught me to close pain gates that way....a HUGE help..he did it for an injury I had prior to getting fibro but I have generalized it....I'll never work a regular job again....Dee Were ages a disability approval factor? > I was warned by my Dr this is very hard to get an approval by. Sometimes > she approves 3rd time. > > My husband was retired at 62 and went six months later for disability and > got it. > > I have a Dr willing to work on the papers with my attorney. I will be 59 > in Dec. and was told by another attny that would help. This attny didn't > say if it would or not. > > I tried in 93 twice and was told no proof I was disabled was presented and > I had Dr's papers from their office as well as a Church showing I was > disabled and they had helped me during the time period I had to have to > qualify. I haven't worked five of the last ten years and that meant they > had to go back that far. > > If I can't get it this go around I will wait until 62 and 7 months ( can't > retire fully until 65 and 7 months so I guess the 7 is added her also), > retire then apply for disability which will give me full benefits. > > I hate to retire early as we are cut all the way down the line then, even > if our husbands pass away and we take their benefits rather than keep ours > as his would be higher. > > Those of you that were turned down or those that got it, do you mind my > asking what your age was at that time? > > > > > > Add or view webpage links about Fibromyalgia/CFS. > http://www.onelist.com/links/ > > > ~*~CHAT TIME:~*~ > MON Night > TIME:Eastern 9 Pm, Central 8 Pm, Mt 7 PM Pacific 6 PM > WHERE: /chat/ > > The_List_Owner@... > > TO unsubscribe. > Go to: http://www.onelist.com/ to this list and unsub from it. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2000 Report Share Posted November 3, 2000 i was 28 when i got it. but it wasnt for fibromyalgia ~~~Tami~~~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2000 Report Share Posted November 3, 2000 Does anyone know how long it takes for soma and percocet to get out of your system.. I need to stop taking so many and I was curious if anyone can help me on this information as well as withdrawl?? I don't want to bring this up with my doctor because I know that i need medications occasionally for fibro.. Any help is greatly appreciated.. thank you Terri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2000 Report Share Posted November 3, 2000 All you said is true, Janice, but may I add what my attny said to us (my friends with SSD and me)? He told us if it was tolerable to get off any pain meds for the day before court, and of course no meds the day of the hearing..if it is okay with the Dr..sleeping the night before may be interrupted, but that's okay as you look the part of the hurting individual you are....and carry meds so you can take them right after the hearing ..Dee Re: Were ages a disability approval factor? > Dear ; > > You asked us: > " Those of you that were turned down or those that got it, do you mind my > asking what your age was at that time? " > > I applied in 1994 for SS disability, due to the fact that surgery brought on > my FM, but at the time I thought it was my recovery that was giving me the > problems not FM. I was turned down and just left it at that. > > In 1998, I reapplied because I was not " recovered " and was then dx with FM > for all my pains and problems of " Fibro Fog " and all the lovely other > symptoms we have. I was lucky because in my first application I did not > count the time before the surgery as I was disabled (I was " out " of it, and > couldn't function due to needing surgery) so they allowed me to add that time > and reapply with " new " evidence. > > I was turned down the first time again, but stuck with it. I finally won the > right to be called Disabled and was awarded retroactive money from when I > first applied to SS. But I needed a lawyer and went to court in front of a > judge. > > That was in 1998, two years ago. I am now 33. I still wish I could work, > and feel bad at times that I can't work, but I need to cope with that and > that is hard. > > One important suggestion that my lawyer told me and that I want to pass on > is, when I went to court she told me not to make it sound better than it is. > Wear your hair the way you always wear your hair, don't get all " dressed up " . > If you have trouble doing things like hair and makeup then don't do it good > for the day in court. Show you as you are normally when you go to court. > > Also, many people feel embarrassed and will not feel good if they really tell > some people how it really is, and they can't admit that they can't do much. > We should, cause it is bad. I remember being asked to tell about my normal > day routine. Well, when I told the judge I felt like saying wow I don't do > much what horror, but I told the truth. I think that that is important, > don't feel embarrassed and feel you need to make yourself look better or say > you can do more than you really can. It will not give the court a true image > of yourself if you make it look better than it is. > > I hope all that made sense and that it might help someone. > > Take care > Janice > > > > Add or view webpage links about Fibromyalgia/CFS. > http://www.onelist.com/links/ > > > ~*~CHAT TIME:~*~ > MON Night > TIME:Eastern 9 Pm, Central 8 Pm, Mt 7 PM Pacific 6 PM > WHERE: /chat/ > > The_List_Owner@... > > TO unsubscribe. > Go to: http://www.onelist.com/ to this list and unsub from it. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2000 Report Share Posted November 3, 2000 i'm not a doctor but in my opinion some of the pills need to be stopped sooner than the day before. Alot of pills like anti-depressants have to be in your system for 3-4 weeks before they are at theraputic strength so it would make sense that they would be in your system at some level for 3-4 weeks after you stop. Some of the supplements also say that it may 2-3 weeks before you see any change. Some pills stay in your system for 2-3 days. If it were me, I would slowly ween myself off all meds starting one med at time about 3 weeks before the hearing to get the full effect. Besides, all the things that I have learned in classes over the years would indicate that you occasionally stop taking a pill to see if it is still producing the desired effects. That is especially important if you take multiple pills. Who knows maybe you stop taking pill C and don't notice any diference in how you feel, so then why spend money taking it. ** , Stinky's caretaker** Just to be is a blessing. Just to live is holy. Rabbi Heschel Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2000 Report Share Posted November 4, 2000 Dee, Thank you for adding that in about not taking meds, cause that would really show how we are. I did not do that, but that would be a great step to take. Much Comfort and Peace Janice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2000 Report Share Posted November 6, 2000 But it sure is a miserable feeling at the time....Dee Re: Were ages a disability approval factor? > Dee, > > Thank you for adding that in about not taking meds, cause that would really > show how we are. I did not do that, but that would be a great step to take. > > > Much Comfort and Peace > Janice > > > > Add or view webpage links about Fibromyalgia/CFS. > http://www.onelist.com/links/ > > > ~*~CHAT TIME:~*~ > MON Night > TIME:Eastern 9 Pm, Central 8 Pm, Mt 7 PM Pacific 6 PM > WHERE: /chat/ > > The_List_Owner@... > > TO unsubscribe. > Go to: http://www.onelist.com/ to this list and unsub from it. > > > > > > Quote Link to comment Share on other sites More sharing options...
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