I am new here. Diagnosed with MS in August 2017 after months of agony and displacement. Anyhooo… I have recently asked my landlord to make adjustments to the bathroom in my flat. I need help sitting down and standing up from the loo. With numb feet and weak hands and a pre-existing Lupus flare up that has seem to have increased with the Copaxone injections I struggle every time I am going to the toilet. Not to mention the weak bladder that doesn’t seem to get better regardless how many Kegels I do a day. The landlord initially refused to make the adjustment. Eventually he issued a section 21 notice and me and my two young daughters are now facing homelessness. I approached the local council and they told me to sit tight until the landlord has a bailiffs order to evict us and then re-approach them again. I did mention to them about my condition but they seem to put that on the deaf. Please help comrades!