*Mention of vomiting, bowel movements, possible ED references and food sensitivity’s
Lets begin which what gastroparesis is, unlike most illnesses with weird names gastroparesis sort of explains it in the name itself, gastro meaning stomach and paresis meaning paralysis, together they mean paralysed stomach.Sounds quite scary right? But without completely freaking you out there are different severities.
This photo is from August 2016, I haven’t been able to take a non bloated picture recently as I always wake up bloated because I still have food in my stomach from the day before. In the first photo my stomach is before I’d eaten anything. I particularly remember my stomach being bad at the time so was mainly eating watermelon and yogurt for a little so I, for once, wasn’t bloated when I woke up. The second photo shows me very bloated after a weekend away in Bath,I hadn’t particularly eaten ‘bad’ foods or over ate. A few hours after this photo was taken and even though I don’t often throw up, my stomach did empty its contents. I had to watermark/write over the image as I don’t want those those juices or weight loss people to promote their annoying products with it.
…
-Diarrhoea and Constipation- I believe that most people already know what diarrhoea and constipation are but why do we have it with gastroparesis? Inevitably with slow mobility of the stomach it has knock on effect to the bowel. Diarrhoea can also be a symptom of constipation and although most people flip between diarrhoea and constipation it can be variable dependent on the person. Chronic diarrhoea and constipation can both have serious side effects. Other then the nausea, bloating and vomiting constipation can, although rare can cause a pseudo-obstruction which is a small bowel obstruction. Chronic diarrhoea, which are watery stools can cause dehydration and malnutrition.
-Pain- Pain is something I initially forgot to write about when I first published this post, I’m not sure why as it’s a huge thing that I struggle to relieve. A lot of medical professionals dispute that there is pain with this condition and although I was lucky with my Drs knowing this, I can undisputedly say it bloody hurts. I go through periods of it not hurting much at all, only a discomfort but then there are times I’m in agony, clutching my Noozie (electric hot water bottle) curled up in bed. I’ve got to clarity that this is only my experience, do not be scared if you’re newly diagnosed reading this, people experience this condition is so many ways, some don’t have much pain at all. Even though I’ve had so many tests done to find the cause of my pain, nothing has been definitive so far. I hope in the future something is found as I believe my pain is something other then gastroparesis but for now I’m put down to that.
…
What are the causes?
There are multiple causes for Gastroparesis, mine like many others is Ehlers-Danlos Syndrome, other main causes are Diabetes, damage during gastric surgery, medications, eating disorders, autoimmune and a highest percentage of cases are idiopathic, meaning they don’t know the cause or trigger for delayed emptying. A small benefit to idiopathic gastroparesis is that people can get better and even recover.
…
Getting diagnosed
Getting diagnosed can be a long process, mainly because it isn’t a well known illness, it’s rare and doctors have to rule out any other causes for delayed emptying, like crohn’s, ulcers, celiac’s, esophagus issues, cancer. For me I had many many blood tests, barium meal, endoscopy, colonoscopy, stool samples, fructose tests and many more. Once all the other possibilities are ruled out then you get sent to have a gastric emptying study.
A gastric emptying study compiles of eating or drinking a radioactive meal. Over 4 hours they will take an x ray intermittently throughout that time. I documented how I felt when I first got diagnosed over on the Gastroparesis |The Truth About Life With A New Diagnosis post.
I’ve got to make it very apparent that I am in no way a medical professional and this post is through my own experience as a person with gastroparesis with an interest in learning as much as I can about this and many other illnesses from medical professionals and other people experiences. I want this post to be a live and open document so please message me or comment down below if there is anything to add or change.
So that’s it, gastroparesis awareness month is nearly over but gastroparesis is a lifelong chronic disorder so awareness shall never be stopped. I hope this post is helpful to you in any way it needs to be and a reminder that if you do have gastroparesis that you are never alone.
Devon x
Last Updated 02/11/17
Due to dyslexia some things may not make sense or are not grammatically correct so please let me know if there are any problems so I can correct it. Thank You 🙂