Guest guest Posted April 22, 2004 Report Share Posted April 22, 2004 In a message dated 4/10/2004 4:36:58 PM Eastern Daylight Time, moondancer@... writes: > I am sorry but am totally misunderstanding the part about you making above > the SSI limit-were you making over 800 dollars? per month? Yes, But ... subtract rent of 940, Medicare and other stuff. You get sick and the final SSD is in a range you barely can keep the place you are at. Or, I just do not qualify for SSI at all. I have/had no resources or a working car after over ten years of being sent home on disability almost every year. And, this recent disability is for five years. With a fixed income, how am I supposed to replace my car, pay car insurance and all those extra things that happen? > I mean I'm sure his income was included in the calculations but I have seen > many couples where both have SSI or SSD........ So I totally don't > understand what they are trying there. His income was ZERO. But that meant nothing they said. He said he was disabled and had not worked since 1997. That also meant nothing. They said my income for family of two, was two much. But if the second person in my house was a child I would have gotten a benefit. If Bill was not my < > spouse I could get benefits. If I had a room mate living with me each could get benefits. But, not the spouse. > I like your idea about rare disease discrimination.............. that was > definitely rude and unfair treatment........ No matter what you have, visible > or not, rudeness should make them lose their jobs... > > Have you talked to your social worker about that.......... I e-mail mine > often......... she normally answers me right back....... that comes in handy > ........ I do not know if she is the Internet type. All this is so new considering I've been ignored ... my whole life until two days before Bill passed. I do not remember who, but I was told to call the cancer doctor office and say I was in crisis. They called me back to ask why. I told them Bill was MY caretaker. They told me but he is dying! He has been in hospital on and off for two months. They asked me what was my disability. I told them. This nurse of course had no clue what EDS was, but she knew what Autonomic Dysreflexia and Autonomic Dysfunction was and was horrified! She called a social worker. Weird. After all this time all it took was for my hubby to be dying :-<. But, I am told not to go there. Because of these events, suddenly I was interviewed by Aging groups and ended up with meal on wheels and a one time rental assistance. This only after they watched me pay ALL my RENT bill and NOT be able to pay for Bills funeral. I suppose, now they believed me. That, by the time I got my SSD and subtracted rent, Medicare, medical insurance, mandatory utilities, Bills prescriptions, my prescriptions, cancer pain medicine, phone, taxi to hospital, doctor office visits, chemo therapy visits, etc. I was " pass " broke. You notice food was not on that list. Nor payment to some twenty or thirty doctors after all those months of hospital meals, test, x-rays, MRI, scans, etc., etc. I now know I was and still is medical indigent. Talk about needing the right keywords to get help. > Keeping all of your situations in my prayers ............ > Hugs and Love- TJ Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2004 Report Share Posted April 22, 2004 In a message dated 4/10/2004 4:36:58 PM Eastern Daylight Time, moondancer@... writes: > I am sorry but am totally misunderstanding the part about you making above > the SSI limit-were you making over 800 dollars? per month? Yes, But ... subtract rent of 940, Medicare and other stuff. You get sick and the final SSD is in a range you barely can keep the place you are at. Or, I just do not qualify for SSI at all. I have/had no resources or a working car after over ten years of being sent home on disability almost every year. And, this recent disability is for five years. With a fixed income, how am I supposed to replace my car, pay car insurance and all those extra things that happen? > I mean I'm sure his income was included in the calculations but I have seen > many couples where both have SSI or SSD........ So I totally don't > understand what they are trying there. His income was ZERO. But that meant nothing they said. He said he was disabled and had not worked since 1997. That also meant nothing. They said my income for family of two, was two much. But if the second person in my house was a child I would have gotten a benefit. If Bill was not my < > spouse I could get benefits. If I had a room mate living with me each could get benefits. But, not the spouse. > I like your idea about rare disease discrimination.............. that was > definitely rude and unfair treatment........ No matter what you have, visible > or not, rudeness should make them lose their jobs... > > Have you talked to your social worker about that.......... I e-mail mine > often......... she normally answers me right back....... that comes in handy > ........ I do not know if she is the Internet type. All this is so new considering I've been ignored ... my whole life until two days before Bill passed. I do not remember who, but I was told to call the cancer doctor office and say I was in crisis. They called me back to ask why. I told them Bill was MY caretaker. They told me but he is dying! He has been in hospital on and off for two months. They asked me what was my disability. I told them. This nurse of course had no clue what EDS was, but she knew what Autonomic Dysreflexia and Autonomic Dysfunction was and was horrified! She called a social worker. Weird. After all this time all it took was for my hubby to be dying :-<. But, I am told not to go there. Because of these events, suddenly I was interviewed by Aging groups and ended up with meal on wheels and a one time rental assistance. This only after they watched me pay ALL my RENT bill and NOT be able to pay for Bills funeral. I suppose, now they believed me. That, by the time I got my SSD and subtracted rent, Medicare, medical insurance, mandatory utilities, Bills prescriptions, my prescriptions, cancer pain medicine, phone, taxi to hospital, doctor office visits, chemo therapy visits, etc. I was " pass " broke. You notice food was not on that list. Nor payment to some twenty or thirty doctors after all those months of hospital meals, test, x-rays, MRI, scans, etc., etc. I now know I was and still is medical indigent. Talk about needing the right keywords to get help. > Keeping all of your situations in my prayers ............ > Hugs and Love- TJ Thanks Quote Link to comment Share on other sites More sharing options...
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