› Forums › General Melanoma Community › Social Security Disability – has anyone lost it after 4 years?
- This topic has 14 replies, 5 voices, and was last updated 6 years, 8 months ago by
WithinMySkin.
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- February 4, 2011 at 6:23 pm
Hi gang. I've been on Social Security Disability for about 5 years due to melanoma. A stage III diagnosis is an automatic yes, and I was Stage IV when I applied. Anyway… I have THANKFULLY been NED for 4 and a half years, and have simply been living my life without the stress of having to hold down a job. Hubby makes a good income, and my disability helps us pay the bills.
Hi gang. I've been on Social Security Disability for about 5 years due to melanoma. A stage III diagnosis is an automatic yes, and I was Stage IV when I applied. Anyway… I have THANKFULLY been NED for 4 and a half years, and have simply been living my life without the stress of having to hold down a job. Hubby makes a good income, and my disability helps us pay the bills.
Well, SS sent me a re-evaluation form to decide if I still need to be on disability. So I'm a bit afraid that they will determine that I'm no longer disabled, even though I'm still considered a stage-IV patient. (I also have lymphedema, which lately has been more of a hindrance than the melanoma has).
If you or someone you know was on SSD for melanoma, and lost it… would you let me know? OR if you've been re-evaluated, and they let you stay on it… please also respond. It would help with my nail-biting!
Love to you all!
Jackie Doss, Stage IV NED… Dallas, TX
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- February 5, 2011 at 6:57 pm
Congratulations on your NED status! Keep going.
I have just been put on SS disability myself. Could you let me know the outcome when you learn the decision? I have been wondering the same thing.
Shelly in Switzerland stage IV
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- February 5, 2011 at 6:57 pm
Congratulations on your NED status! Keep going.
I have just been put on SS disability myself. Could you let me know the outcome when you learn the decision? I have been wondering the same thing.
Shelly in Switzerland stage IV
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- February 6, 2011 at 3:05 am
Hi Jackie, I am in the appeal process for 5 months now. I have been stage IV for 4 years and for 3 years of that I have been NED . I was sent the redetermination application after 3 years on disability and was turned down. Feel free to e-mail me and I will tell you more about this.
The disability redetermination person got my Oncologist to approve moving up the date of my yearly PET scan ( to next week) so that at least I will have that covered by medicaid/medicare this month if he ends up turning me down.
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- February 6, 2011 at 3:05 am
Hi Jackie, I am in the appeal process for 5 months now. I have been stage IV for 4 years and for 3 years of that I have been NED . I was sent the redetermination application after 3 years on disability and was turned down. Feel free to e-mail me and I will tell you more about this.
The disability redetermination person got my Oncologist to approve moving up the date of my yearly PET scan ( to next week) so that at least I will have that covered by medicaid/medicare this month if he ends up turning me down.
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- February 12, 2011 at 2:15 am
Hi, Jackie.
You and I are about on the same time table with our stage IV diagnosis….I haven't been on here for awhile so it's great to see you doing well. As to your question/concern about disability….
Since being diagnosed stage IV Feb. of '05, I didn't apply for disability until Oct. of '07 after a relapse. I have also chosen quality of life and remained on disability since that time. I am on STRS of Ohio disability. Last summer ('10) STRS requested a review of my case. I was worried too because while I am healthy-looking at present, but the entire process and lingering effects of both the treatment and emotional/mental trauma of living with mel has left me a different person than I was before (as I'm sure you know).
I worry about the stress of the effects and the job (teaching) taking a toll on me again (keep doing what's working…right?)
My lead oncologist asked me what I wanted to do and I told him my concerns and he said, "I completely agree. This is not a disease with which to take risks…(additionally) given the uncertain climate of the healthcare system, I wouldn't want you to leave the system because it might be very difficult to get back on. I know what it takes to keep you on but I can't guarantee I can get you back."
Enough said. He filled out the paperwork and my review was accepted as plausible by the disability board and I was renewed.
Talk to your doc. Speak your concerns and I'm sure they'll agree.
Take care,
Karen
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- February 12, 2011 at 2:15 am
Hi, Jackie.
You and I are about on the same time table with our stage IV diagnosis….I haven't been on here for awhile so it's great to see you doing well. As to your question/concern about disability….
Since being diagnosed stage IV Feb. of '05, I didn't apply for disability until Oct. of '07 after a relapse. I have also chosen quality of life and remained on disability since that time. I am on STRS of Ohio disability. Last summer ('10) STRS requested a review of my case. I was worried too because while I am healthy-looking at present, but the entire process and lingering effects of both the treatment and emotional/mental trauma of living with mel has left me a different person than I was before (as I'm sure you know).
I worry about the stress of the effects and the job (teaching) taking a toll on me again (keep doing what's working…right?)
My lead oncologist asked me what I wanted to do and I told him my concerns and he said, "I completely agree. This is not a disease with which to take risks…(additionally) given the uncertain climate of the healthcare system, I wouldn't want you to leave the system because it might be very difficult to get back on. I know what it takes to keep you on but I can't guarantee I can get you back."
Enough said. He filled out the paperwork and my review was accepted as plausible by the disability board and I was renewed.
Talk to your doc. Speak your concerns and I'm sure they'll agree.
Take care,
Karen
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- February 12, 2011 at 2:15 am
Hi, Jackie.
You and I are about on the same time table with our stage IV diagnosis….I haven't been on here for awhile so it's great to see you doing well. As to your question/concern about disability….
Since being diagnosed stage IV Feb. of '05, I didn't apply for disability until Oct. of '07 after a relapse. I have also chosen quality of life and remained on disability since that time. I am on STRS of Ohio disability. Last summer ('10) STRS requested a review of my case. I was worried too because while I am healthy-looking at present, but the entire process and lingering effects of both the treatment and emotional/mental trauma of living with mel has left me a different person than I was before (as I'm sure you know).
I worry about the stress of the effects and the job (teaching) taking a toll on me again (keep doing what's working…right?)
My lead oncologist asked me what I wanted to do and I told him my concerns and he said, "I completely agree. This is not a disease with which to take risks…(additionally) given the uncertain climate of the healthcare system, I wouldn't want you to leave the system because it might be very difficult to get back on. I know what it takes to keep you on but I can't guarantee I can get you back."
Enough said. He filled out the paperwork and my review was accepted as plausible by the disability board and I was renewed.
Talk to your doc. Speak your concerns and I'm sure they'll agree.
Take care,
Karen
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- February 12, 2011 at 2:15 am
Hi, Jackie.
You and I are about on the same time table with our stage IV diagnosis….I haven't been on here for awhile so it's great to see you doing well. As to your question/concern about disability….
Since being diagnosed stage IV Feb. of '05, I didn't apply for disability until Oct. of '07 after a relapse. I have also chosen quality of life and remained on disability since that time. I am on STRS of Ohio disability. Last summer ('10) STRS requested a review of my case. I was worried too because while I am healthy-looking at present, but the entire process and lingering effects of both the treatment and emotional/mental trauma of living with mel has left me a different person than I was before (as I'm sure you know).
I worry about the stress of the effects and the job (teaching) taking a toll on me again (keep doing what's working…right?)
My lead oncologist asked me what I wanted to do and I told him my concerns and he said, "I completely agree. This is not a disease with which to take risks…(additionally) given the uncertain climate of the healthcare system, I wouldn't want you to leave the system because it might be very difficult to get back on. I know what it takes to keep you on but I can't guarantee I can get you back."
Enough said. He filled out the paperwork and my review was accepted as plausible by the disability board and I was renewed.
Talk to your doc. Speak your concerns and I'm sure they'll agree.
Take care,
Karen
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- September 24, 2016 at 8:18 pm
You can find the requirements for social security disability under section 13.29 on their website: https://www.ssa.gov/disability/professionals/bluebook/13.00-NeoplasticDiseases-Malignant-Adult.htm#13_03Lauren
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- September 24, 2016 at 8:18 pm
You can find the requirements for social security disability under section 13.29 on their website: https://www.ssa.gov/disability/professionals/bluebook/13.00-NeoplasticDiseases-Malignant-Adult.htm#13_03Lauren
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- September 24, 2016 at 8:18 pm
You can find the requirements for social security disability under section 13.29 on their website: https://www.ssa.gov/disability/professionals/bluebook/13.00-NeoplasticDiseases-Malignant-Adult.htm#13_03Lauren
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