I ask this because it profoundly affects my med coverage. Even with my disability, I make too much for Medicaid and Medicare, yet I can get Medicaid because of my extremely high med. costs only with a spend down of about 1000 a month..that's right, 1000 a month! Medicare usually paid for my nebulized meds, such as TOBI, which I know all of you are aware of how much that one costs, Xopenex as well as Mucomyst 100% with my medigap insurance. Now...once January 1st comes rolling around, that won't be so, I have talked with at least a few folks from Medicare myself. It all falls under the Medicare part D prescription plan. I will now have to pay a substantial co pay for my meds, especially the TOBI...I have narrowed my choices down to 3 insurance companies as I am also on several other meds. Pancrease was another one I have had to consider as well...that bottle of 100 caps costs $200 a bottle!!!
I am just wondering what all of you folks on SSDI are going through with the Medicare issues, especially those who aren't on Medicaid or state help. My social worker from my Medicaid office is supposed to get back with me, she is doing the best she can, she feels terrible for me as far as my med plight goes. IV meds are a nightmare, I have found some companies that will cover them, so I am not complaining there....I just plugged in the most common IV meds I am on and looked at the costs...some are actually reasonable and I would gladly pay those co pays to avoid a hospital stay any day. But its the nebs and pancrease I am worried about....any other suggestions out there? I am so worried about this financially, as I know others on this board are as well. Dont get me wrong, I am glad that I do have insurance and that Medicare does indeed pick up a huge amount of my tab as far as my ventilators go and their supplies ($60,000 a year just f or that)...but I am a single parent, live on SSDI and have two kids to raise (do get child support to help thank god!). Mom is home full time to make sure that I am safe and to help me physically...so I really am in a pickle as they say. Like I have said in the past, I feel very comfortable talking to all of you here, I know alot of you have walked in my shoes and can relate to my problems. Thank you all in advance for your consideration and help here...as Jan 1st gets closer, I am getting more frustrated. Hugs to all, Jenn <img src="i/expressions/face-icon-small-smile.gif" border="0">
I am just wondering what all of you folks on SSDI are going through with the Medicare issues, especially those who aren't on Medicaid or state help. My social worker from my Medicaid office is supposed to get back with me, she is doing the best she can, she feels terrible for me as far as my med plight goes. IV meds are a nightmare, I have found some companies that will cover them, so I am not complaining there....I just plugged in the most common IV meds I am on and looked at the costs...some are actually reasonable and I would gladly pay those co pays to avoid a hospital stay any day. But its the nebs and pancrease I am worried about....any other suggestions out there? I am so worried about this financially, as I know others on this board are as well. Dont get me wrong, I am glad that I do have insurance and that Medicare does indeed pick up a huge amount of my tab as far as my ventilators go and their supplies ($60,000 a year just f or that)...but I am a single parent, live on SSDI and have two kids to raise (do get child support to help thank god!). Mom is home full time to make sure that I am safe and to help me physically...so I really am in a pickle as they say. Like I have said in the past, I feel very comfortable talking to all of you here, I know alot of you have walked in my shoes and can relate to my problems. Thank you all in advance for your consideration and help here...as Jan 1st gets closer, I am getting more frustrated. Hugs to all, Jenn <img src="i/expressions/face-icon-small-smile.gif" border="0">