I’ve never fully recounted my experience with state assistance, Medicaid and food stamps that I received while pregnant with the Munchkin. I still hold a lot of shame, not specifically attached to the receipt of said assistances, but from the reactions of others while I was utilizing government funded programs.
People were downright nasty to me. Family members. “Friends.” Co-workers. The staff at my doctor’s office. The staff at the hospital. The social workers themselves (and it got worse later on). My landlord. A pharmacy worker. The people at my current church who didn’t know I was once on assistance but launched into a tirade about those who are. The list goes on.
But there were compassionate people. The first time I showed up at the grocery store to use my EBT card, I had no idea how to go about it. The cashier was kind. Her tone was one of compassion. She taught me not only about my purchases at that store, but how to use it elsewhere. I still have a vivid memory of leaving that store and thinking that good people did exist.
It was really hard for me to stay on assistance due to my kidney disorder that landed me on bed rest at 18 weeks. Level 3 bed rest, mind you. I was unable to work. I was also unable to drive. So, when I would miss a visit with my social work regarding my lack of employment seeking, they would cut me off of assistance. I would then break bed rest, whcih was really dangerous for me to do, and get back to the office. Remind them. Show them my forms. And be fine again. For awhile. I was cut off twice during the pregnancy… and again right at the end. I paid for Munchkin’s birth out of pocket… for years. I just recently paid it off.
I’ve been asked why I didn’t go back in right after birth and get put back on assistance. The social worker on my case was so incredibly rude to me when I admitted, somewhere in the 8th month of pregnancy, that I would be placing my daughter for adoption. She verbally lashed me for “working the system” and taking money from people who really needed it. She yelled for a good twenty minutes. There was no way I was going back in to that office and asking for my birth to be covered when I didn’t have a baby to show for it. I left Pennsylvania six days after Munchkin’s birth.
I am grateful that the assistance did cover what it did. As I said, I had a ridiculously complicated pregnancy. The assistance covered my first lengthy hospital stay when my kidney disorder was found. It covered that first surgery. A second lengthy hospital stay. A third surgery and that hospital stay. Four L&D trips in which I was in preterm labor due to said kidney disorder and the medications I needed to take to combat the labor, dilation and constant contractions. An ER visit for heavy labor, a subsequent trip to Pittsburgh via ambulance (lights and sirens) and that lengthy hospital stay. That last hospital stay was actually what ended up cutting my benefits. I missed an appointment at the office while I was fighting for my life and my daughter’s life in a hospital bed in Pittsburgh. Two weeks later, they cut me, but I didn’t receive notice as my parents had me staying in their house as my doctor’s had said labor would be soon. I found out about my cut benefits about six hours after the Munchkin arrived.
Due to my experience, I have a lot of compassion for people on assistance. That’s why I felt a lot for this writer at BlogHer who talked about judgments passed on people who are on assistance having things like cell phones or the Internet. And that’s why my vision kind of shakes and I can’t form coherent sentences when people spout of nasty things in the comments or on Facebook in reply to posts like that. I can tell, immediately, that those people have never had to fight for their life, for their unborn baby’s life, while trying to stay on assistance. That they’ve never had a social worker yell thisclose to their face. That they’ve never felt the shame and stigma of both accepting assistance and relinquishment. I try to force myself to realize that not everyone wants to understand the plights of others, but it just breaks my heart for those that are continuously stereotyped by those who don’t even want to understand.
I get so discouraged with society when we let the negative define a whole group of people. If we all did that, we should say that everyone who is not on assistance is a nasty, prejudicial, compassion-less meanieface. If we know that not to be true, why can’t we stop stereotyping those utilizing services?