H
HeadCracker
Guest
Hello everyone,
My doc did an MRI on me recently and showed moderately severe lurabar (L4-L5) spinal stenosis with narrowing of the central canal throughout// Further tests show that its not due to bone but more tissue which points to the fact that i was probably born with this and at my age, I am starting to feel what i believe i have been living with for some time.. I have, for a couple of years, lived with my hanRAB being very stiff in the mornings and I have to wake in the middle of the night to tell myself to relax them.. ( When i went to the doc initially, I was having dull low back pain and it was very bad).. I apparently had seen the doc last year for the same issue and forgotten about it. I am normally very active and healthy and don't go to see the doc very often. After waiting for the doc to order the MRI.. my legs started spasm-ing and tingling a lot like my hanRAB do.. It has been about a month now and more test have been ran and my leg spasms have turned into pain, pins/ needles and twitching. It is a very scary feeling, really.. but makes sense to me because even brushing my teeth i am compelled to lean on the sink and similar things around the house.
As i type this my hanRAB keep wanting to flinch and my positioning for sitting for a long period of time is limited.. My balance has always been off and i have always been very clumsy.. (its even a family joke).. My quality of life has been limited all of the sudden and I admit I am not a good patient.. I don't like being in-active at home. I have a 15 year old as well as a 3 year old (both beautiful girls) and I don't like feeling worthless.
I am worried about permanent nerve damage as I don't know what exactly to look for. I know the feeling of my legs and hanRAB wanting to move on their own is not a good sign but i am not sure what else to look for. The first specialist said i will likely have surgery in the future and wanted to hold off as long as possible, and to try injections but I have to wait until Dec. 20th and our insurance rates will go up considerably next year. I am pondering why we should inject and take a chance at that not helping especially since he admitted i will probably have to have a surgery. I wonder if i should opt to get an elective surgery to fix the problem now? ALSO: I read that this is a disease that mostly affects older patients.. and the idea of me living with this for any more time makes me worry about permanent nerve damage. BECAUSE of my younger age - wouldn't it be better to get a surgery sooner than later ? I would bounce back quicker/ Correct? I am just confused and its a lot to take in and think about.
Thanks for taking the time to read my conundrum.// I would appreciate any comments.
My doc did an MRI on me recently and showed moderately severe lurabar (L4-L5) spinal stenosis with narrowing of the central canal throughout// Further tests show that its not due to bone but more tissue which points to the fact that i was probably born with this and at my age, I am starting to feel what i believe i have been living with for some time.. I have, for a couple of years, lived with my hanRAB being very stiff in the mornings and I have to wake in the middle of the night to tell myself to relax them.. ( When i went to the doc initially, I was having dull low back pain and it was very bad).. I apparently had seen the doc last year for the same issue and forgotten about it. I am normally very active and healthy and don't go to see the doc very often. After waiting for the doc to order the MRI.. my legs started spasm-ing and tingling a lot like my hanRAB do.. It has been about a month now and more test have been ran and my leg spasms have turned into pain, pins/ needles and twitching. It is a very scary feeling, really.. but makes sense to me because even brushing my teeth i am compelled to lean on the sink and similar things around the house.
As i type this my hanRAB keep wanting to flinch and my positioning for sitting for a long period of time is limited.. My balance has always been off and i have always been very clumsy.. (its even a family joke).. My quality of life has been limited all of the sudden and I admit I am not a good patient.. I don't like being in-active at home. I have a 15 year old as well as a 3 year old (both beautiful girls) and I don't like feeling worthless.
I am worried about permanent nerve damage as I don't know what exactly to look for. I know the feeling of my legs and hanRAB wanting to move on their own is not a good sign but i am not sure what else to look for. The first specialist said i will likely have surgery in the future and wanted to hold off as long as possible, and to try injections but I have to wait until Dec. 20th and our insurance rates will go up considerably next year. I am pondering why we should inject and take a chance at that not helping especially since he admitted i will probably have to have a surgery. I wonder if i should opt to get an elective surgery to fix the problem now? ALSO: I read that this is a disease that mostly affects older patients.. and the idea of me living with this for any more time makes me worry about permanent nerve damage. BECAUSE of my younger age - wouldn't it be better to get a surgery sooner than later ? I would bounce back quicker/ Correct? I am just confused and its a lot to take in and think about.
Thanks for taking the time to read my conundrum.// I would appreciate any comments.