So....here's a little update that's frustrating.
In a nutshell, I need a powerchair but my home is a split level with no bathroom or bedroom on the first floor. Therefore, I'm told I would be turned down if I went through the pt eval. and tried to get one through my insurance.
Had a contractor come and look over my home, taking measurements, etc. to give me an estimate on renovations. He was referred to me by a friend because he is not expensive and is very reliable. Even so, with all of the remodeling/renovations added up, it seems to make more sense to just look for a new house.
Problem: We don't have anything in savings to go towards a downpayment. We would be able to afford a house comparable in size to the one we have, but were not prepared for this so soon.
So...I'm THANKFULLY able to use a power chair (borrowed) at work, but have to keep it there. Our minivan is not set up for transporting a power chair (another down-the-road cost, if I ever GET the power chair). Still relying on my visiting parents to take me back and forth to work , using my manual wheelchair (a true blessing that I bought online a few years ago for theme parks) to take me from the car to the building and my office.
The ONE thing that was SUPPOSED to be easy was for me to get AFOs for each foot. Turns out that the first recommended place to get them custom-made (a must, according to my PT), was not on the list of providers for my insurance company. Took TWO days of calls and frustration with the ins. website to finally find one. It was one that my dad had found earlier in the phonebook! Just relieved to find an approved place and get an appointment.
So...what does one DO in the "in-between" time before being able to even qualify (house-wise) for a power chair??? My poor hubby (works full-time as a math instructor at the same college where I'm an adjunct) and my parents are being stretched thin "picking up the slack" as I am still enduring this flare. They don't live here permanently, but do have their own space for when they visit.
I am frustrated at how dependent I am on them, how difficult it is for me to get around most of the time (brief moments of walking ok before fatigued), how difficult it is to keep up with my grading/planning, and how much I am missing out on with my kids when I'm not doing well.
Prayers are not only welcome, but HIGHLY encouraged! As much as I know and believe that God has things in control, I am still subject to feeling overwhelmed and confused.
Thanks for letting me vent a bit. Oh....I DO have an appt. with OVR next week, and I DID get some GREAT info. from NMSS (although most of it is for remodeling and many sources for help are based on low income; not as helpful if you mainly need a downpayment and have just not been wise enough to save money ).
I guess this is an "I really hate MS day/semester."
In a nutshell, I need a powerchair but my home is a split level with no bathroom or bedroom on the first floor. Therefore, I'm told I would be turned down if I went through the pt eval. and tried to get one through my insurance.
Had a contractor come and look over my home, taking measurements, etc. to give me an estimate on renovations. He was referred to me by a friend because he is not expensive and is very reliable. Even so, with all of the remodeling/renovations added up, it seems to make more sense to just look for a new house.
Problem: We don't have anything in savings to go towards a downpayment. We would be able to afford a house comparable in size to the one we have, but were not prepared for this so soon.
So...I'm THANKFULLY able to use a power chair (borrowed) at work, but have to keep it there. Our minivan is not set up for transporting a power chair (another down-the-road cost, if I ever GET the power chair). Still relying on my visiting parents to take me back and forth to work , using my manual wheelchair (a true blessing that I bought online a few years ago for theme parks) to take me from the car to the building and my office.
The ONE thing that was SUPPOSED to be easy was for me to get AFOs for each foot. Turns out that the first recommended place to get them custom-made (a must, according to my PT), was not on the list of providers for my insurance company. Took TWO days of calls and frustration with the ins. website to finally find one. It was one that my dad had found earlier in the phonebook! Just relieved to find an approved place and get an appointment.
So...what does one DO in the "in-between" time before being able to even qualify (house-wise) for a power chair??? My poor hubby (works full-time as a math instructor at the same college where I'm an adjunct) and my parents are being stretched thin "picking up the slack" as I am still enduring this flare. They don't live here permanently, but do have their own space for when they visit.
I am frustrated at how dependent I am on them, how difficult it is for me to get around most of the time (brief moments of walking ok before fatigued), how difficult it is to keep up with my grading/planning, and how much I am missing out on with my kids when I'm not doing well.
Prayers are not only welcome, but HIGHLY encouraged! As much as I know and believe that God has things in control, I am still subject to feeling overwhelmed and confused.
Thanks for letting me vent a bit. Oh....I DO have an appt. with OVR next week, and I DID get some GREAT info. from NMSS (although most of it is for remodeling and many sources for help are based on low income; not as helpful if you mainly need a downpayment and have just not been wise enough to save money ).
I guess this is an "I really hate MS day/semester."
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