In May 2006  I was experiencing vision problems. I was asked to see a neurologist by my eye doctor. At that time I was unofficially diagnosed with MS.  In March of 2010, I experience my first MS exerbation body numbness and falling...I wish i could say...i got better with time..but it did not work out that way for me unfortunately. I gradually went from crutches..to walker...now wheelchair...My recent trip to the neurologist wasn't the best. I have not been able to walk on my own for some time now...but since January it has been hard to fuction. My legs are not bending most days.. i have falling several times and at times have to get around my home sitting on my butt. Because we have a split entry home...the insurances refuse to fund any chair that is motorized since we have stairs in our house. When i do manage to leave my home...when i come back i'm so exhausted that i have issues getting up to the upstairs living space. I have asked for assistance for funding a bathroom downstairs as well as for this machine RT300 that helps with my lefs spasms. ..but have been also denied  Trying to get my main living space down stairs all together. My mobility lately hasn't been the best..possibly the worst i have ever felt.  I have a little daughter. I want to be able to function and have a better quality of life for her.  My little daugther tells me how she wants to be a chef just like me. I'm  just trying to be there for when that time comes.  I am just trying  to have a better  quality of life now ...so I can be there for whatever she needs me for. I know a cure will be here soon until then I have to keep on enduring.  Unfortunately for some reason insurance companies and non profits have yet to make any attempts to help..so I am humbling myself and reaching out to the world to help my family. I want anyone who is willing to help to know that these funds will be used for what they were requested for. I will appreciate everyone of you for the rest of my life. I thank you in advance from the bottom of my heart.