The last two months have been the hardest in my life

Adelyn Lyon

It’s August 1st, which means it’s the start of Gastroparesis Awareness Month. I’m now 1 year and 9 months into my journey, and it’s been a harder year than I ever expected (and that is after losing 60lbs my first year). In the last year, I’ve had to go on leave from teaching, had 5 feeding tube exchanges, been hospitalized 23 days total, and had too many blood draws, IVs for hydration, doctor appointments, procedures, and ER visits to count. (Not to mention trying to parent and homeschool during a pandemic through all of this).

The last two months have been the hardest of my life, with a new flare that will not end and is keeping even my feeding tube from working properly. I’ve lost the 15 lbs I had managed to regain in the fall, plus an additional 8, making my loss 23 lbs in less than two months. I will likely keep losing weight while we figure out a solution and am now getting close to being underweight. I have a big procedure this Wednesday which might be my chance at finally feeling better and could use all the positive thoughts that it will be successful. This has to work because there aren’t really any other good options left. My doctor basically told me that my choices might be between using opiates, which would likely cause a dependence and may end up hospitalizing me bc I’m unlikely to tolerate withdrawal safely, or TPN, nutrition through my veins, which has a high risk of blood or heart infections, severe organ damage and sepsis. There should be better options. I’m only 34.

My situation isn’t unique among people with gastroparesis. And without a cure or funding, we will continue to be treated like drug seekers, or accused of having an eating disorder, or told we need to be more positive, or told we just need a therapist bc we’re “too young and sweet” to have a feeding tube, or refused care because we “seem healthy” despite how awful we feel from prolonged starvation (I have been told all of these things by doctors). We deserve respect from the medical community, to be taken seriously, and to have real options and care for a better life.

After over a year of hard work, our House Bill for GP Awareness only has 22 co-sponsers out of 435. Please, please help by supporting our bill. It will give us the awareness and funding we need to live. Please help save lives.

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Diagnosed after 7 years of symptoms

Josh Tewsley

I am asking my legislator to support this bill on behalf of myself and the many other Gastroparesis Warriors across this country who fight Gastroparesis and it’s debilitating symptoms on a daily basis.


Gastroparesis, or paralysis of the stomach is a rare disease that affects only a small percent of the U.S population and not many more than that worldwide.


I was officially diagnosed with Gastroparesis in January of 2019 after enduring symptoms of the disease for more than seven years. Because Gastroparesis is considered a rare illness, knowledge of it is severely limited. Many people, including myself go misdiagnosed for many years before being officially diagnosed with the disease. Many doctors have never even heard the term Gastroparesis, let alone it’s life altering symptoms. This disease does not only go misunderstood in the physician community but also with our families, friends, co-workers, and bosses. Because Gastroparesis is on the inside, often times we may look ok on the outside leading to ridicule and judgement from other’s. We may look ok on the outside, bet are literally starving on the inside. We may look ok to others but we had just been literally throwing our guts out moments before. We may look fine to other’s but we had just gotten out of the hospital because this disease knocked us down.


I am supporting this piece of legislation because of the fact that that person is me. I have had my life stolen right out from under me. I can no longer work because of Gastroparesis. Because of the life altering consequences of Gastroparesis I can no longer be the husband or the father that I strive so hard to be. I support this legislation because there is currently NO cure for Gastroparesis and treatment options are severely limited with many treatments not even helping the symptoms of this disease at all. We are a large group of misunderstood people fighting for our lives. We have cures and treatment for cancer and other illnesses that affect American people throughout and while I am not downplaying those diseases at all, I want to see Gastroparesis research to be better funded so those who come after us can have a legitimate chance of leading a normal life.


Lastly I advocate for this disease because it is the right thing to do. I want people to understand what we go through every day and what risks are associated with Gastroparesis. My message is simple, let’s find a cure, let’s find better treatments for Gastroparesis however we cannot do any of that without support and increased funding.

Thank you very much,
Joshua Tewsley
Louisville Kentucky resident
Gastroparesis Advocate

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