MS sucks

My name is Aisha, I'm 34 and I'm fundraising for mobility aids such as an motorized wheelchair, ramps and hopefully a vehicle that I can use to get myself to and from my various medical appointments and therapy sessions. I was diagnosed with aggressive Multiple Sclerosis (MS) in 2020 and have been unable to walk since then. I am numb from my waist down and have extreme weakness in my legs. I woke up one day unable to walk and unable to use the bathroom. I became incontinent and have to use a Foley catheter. I was working my dream job as a Bridge Operator but am currently unable to work because I cannot climb the stairs to the bridge house. The fatigue I get is unbearable and so is the horrible, burning pain I am constantly in. I also have a seizure disorder that was caused by MS. The brain fog also comes at the worst times and I don't want to put anyone's life in danger, so I was let go from my job that had health insurance, life insurance and retirement benefits. I lost it all. I am disabled and get just $900 a month to cover my bills and everything else I need which is impossible. Pushing myself around in manual wheelchair is too exhausting and motorized wheelchairs are too expensive. No help exists for people in my situation and it's painful and frustrating. I don't know where else to go or what else to do. I don't have any social media or friends to reach out to for help. I am hoping this will give me some relief. Thank you in advance from the bottom of my heart to anyone who can and does help me. May GOD bless your beautiful heart!