Lakshmi Faith’s Story

Hello, my name is Lakshmi, and I’m a 31-year-old female.  I started to get sick at the age of 14 years old.  I’ve been suffering over 17 years now with severe abdominal pain; nausea; vomiting; diarrhea; endometriosis, which causes me to bleed heavily, makes me very dizzy, and causes severe migraines that last from 1-2 weeks straight every month; and anemia.  I came into the emergency room on Friday, March 20, 2015, and am currently admitted for dehydration and pain.

I’ve been hospitalized more than 480 days in the last 17 years.  It’s a daily struggle living with gastroparesis; I’m usually admitted 2-3 times a month for it.  I’ve lost most of my veins already.  My IV lines are usually in my neck, fingers, palms, groin, legs, feet, and toes.  I’ve had ports and PICC lines.  I usually get stuck 10-15 times before they find a good line.

Gastroparesis has caused other health issues as well.  I’ve developed over $12000 worth of dental problems that insurance does not cover.  I’ve spent many birthdays and holidays in the hospital.  It’s a living nightmare, and I wouldn’t wish it on my worst enemy.

Imagine starving to death but not being able to eat, not being able to sit or stand up straight.  Your daily goal to achieve is to be able to eat and drink a little, making sure it stays down, and to be able to stand up long enough to take a shower.

I can go on and on and write a book or two on the daily struggles of living with gastroparesis.  I am one of the 5 million Americans who are suffering from this nasty, cruel disease, and I’m asking you all to please help spread awareness of this deadly disease so that more research can be done and we can have the opportunity to eat every day like everyone else.  Please help!  I’ve already lost one of my good friends, Ashley Gillmore, to this disease (last July) as well as a few members of my Facebook support group.  Recently, we lost a young, handsome toddler boy.  Too many of us are suffering and dying every day.  We desperately need help, so please, I am begging you all to help spread awareness of gastroparesis.  Thank you!

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About the author: Gastroparesis: Fighting For Change Admin

We created this website to provide the public with additional information regarding Gastroparesis. It is our goal to connect users with our Facebook advocacy group, “Gastroparesis: Fighting for Change.”

Our Gastroparesis: Fighting for Change Facebook group was formed to unite people with Gastroparesis and other digestive and motility disorders to work for change. It is not a typical GP support group, as we do not discuss personal medical issues. Rather, we established this as a place where members can discuss ideas regarding our mission, vision, goals, needs, services, and resources to work toward solutions. So if you want to make a difference for our GP community, we encourage you to share your ideas! Additionally, we need you to help us fight for changes in legislation! Also, you can help raise funds! Finally, you can help spread awareness! Please join our main group. We would love to have you!

You can find links to our Community Page and our Advocacy Group on our Resources Tab.

In order to accomplish our goals, we will be sharing many ways you can get involved on our Campaigns Tab.

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