First a little history. i am 55 years old and type one since the age of 5. i am on s.s. disability due to my numerous health problems most due to 50 years of diabetes. i have been on a pump for about 9 years and love it but today i had to tell my doctor i needed to go back to injections and another type of insulin due to not being able to afford the humalog anymore. now here is why, medicare part B will pay for insulin if you are on a pump. I had been getting my insulin through Liberty medical on my part B but the stopped providing it last year and there is no one else that will do it on part b either. i have called every pharmacy and mail order supplier with no luck. I have called medicare and gotten list from them that were suppose to be providers but none were. I was left with getting my humalog through my medicare part D prescription insurance which has a #2900 a year limit. 3 vials of humalog cost $527 which i pay $40 and my part D pays $487. long story short is with all my meds i hit my part D limit in 4 months so for the next 8 months i would have to pay for all my meds myself which i can not afford to do. i hate to go back to injections but i have no choice. What i cant understand is why with places like this and the american diabetes ■■■. there is no one out there fighting the government fo us on this horrible problem. i can not be the only one in this situation. we need help with this and we need someone or some group to fight for us so we can get the meds we need.