#GPawareness
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August is Gastroparesis Awareness Month. I was diagnosed with this disease December 26, 2017. Merry Christmas to me right? My main symptoms are extreme nausea, bloating, pain, early satiety, bowel issues, fatigue and not being hungry. I have dropped from 308lbs to now 216lbs and going since about a year before my official diagnosis. I miss food. I mainly eat a liquid/soft food diet that relies heavily on processed food. It's the easiest for my stomach to digest.
#gastroparesis#spoonie#chronically ill mom#chronically ill#spooniestrong#spoonielife#gpwarrior💚#gpawareness
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I have been working on this topic and this article for quite a while. Thank you for your patience, and I appreciate you guys giving me the time to write it, as I wanted to be as detailed as possible and give as much information as I could, so that people can make an informed and educated decision on whether medical marijuana is right for them:
http://www.emilysstomach.com/2019/03/the-benefits-of-cannabis-for.html
I have always been an advocate for it. It has helped so many people I know.
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy #medicalmarijuana #marijuana #cannabis
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August is Gastroparesis Awareness Month 💚 #gastroparesisawareness #gastroparesis #gp #gpawareness
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My night with tube feeding for gastroparesis. Bleh.
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#lovewins #chronicillness #diabetes #feelgoodwishes #gastroparesis #gpawareness
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I made this little graphic for all my #GP or #gastroparesis people out there. I've tried to write a post that inspires people, but it's hard when you're exhausted and feel like giving up. I want nothing more than to cry to my good ol friends Ben & Jerry, but know if I do, I'll just feel a thousand times worse. To all my fellow #Spoonies, we're all suffering in this together. #done #GPAwareness #StarvingForACure #TheMoreYouKnow #FuckGastroparesis
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#gastroparesis #gpawareness #spoonie #chronicillness #invisibleillness #findacure
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Heyy everyone!! August is Gastroparesis Awareness Month! The "color" for GP is green so in order to raise awareness I encourage everyone to post a picture of yourself wearing green! Gastroparesis for short means that your stomach is paralyzed. You get sick very easily and there is nothing you can do about it but fight! So I encourage everyone to raise awareness! Not only for me but for all of the other people that are fighting! Thank you in advance. #gastroparesis #GPAwareness
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A Questionnaire
Invisible Illness Survey!
1. The illness I live with: Celiac & Gastroparesis!
2. I was diagnosed with it in the year: 2013 bro
3. But I had symptoms since: I’ve had a shit stomach since I was born.
4. The biggest adjustment I’ve had to make is: no work. Barely eating.
5. Most people assume: I have no idea.
6. The hardest part about mornings are: morning sickness yo
7. My favorite medical TV show is: Food Network. It is my addiction.
8. A gadget I couldn’t live without is: my blender
9. The hardest part about nights are: Ever since I was little, I had nightmares when I was nauseous while asleep. Now I have been having nightmares every night.
10. Each day I take __ pills: 11!
11. Regarding alternative treatments: Considering, doing the research
12. If I had to choose between an invisible illness or visible I would choose: This question is such an asshole. It sucks if someone is sick and is in a wheelchair. It sucks if someone isn’t but feels pain. I would choose no illness.
13. Regarding working and career: ): Med leave, considering other jobs
14. People would be surprised to know: About the job situation.
15. The hardest thing to accept about my new reality has been: the job situation. Also like not being able to eat foods.
16. Something I never thought I could do with my illness that I did was: enjoy cupcakes (gfree) and fruits (smoothies for the win)
17. The commercials about my illness: HAHA . JOKES.
18. Something I really miss doing since I was diagnosed is: running around Disney parks, and volunteering. Also alcohol!
19. It was really hard to have to give up: STEAK and normal pasta, and driving
20. A new hobby I have taken up since my diagnosis is: reading all books ever.
21. If I could have one day of feeling normal again I would: go to the magic kingdom, hop to epcot, have a margarita at mexico and a bowl o’pasta at Italy, and go to texas de brazil for an enormous, gluten and hard-to-digest MEAT dinner
22. My illness has taught me: that every day is a new day.
23. Want to know a secret? One thing people say that gets under my skin is: when people say “when you’re better, we’ll ….” I may not be getting better anytime soon.
24. But I love it when people: make the effort to see me, and gentle adventures. Also texting.
25. My favorite motto, scripture, quote that gets me through tough times is: Joshua 1:9 (Have I not commanded you? Be strong and courageous. Do not be terrified; do not be discouraged, for the LORD your God will be with you wherever you go.) Phillipians 4:13 (I can do all things through Christ who strengthens me)
26. When someone is diagnosed I’d like to tell them: You’ll have decent days. Also, smoothies.
27. Something that has surprised me about living with an illness is: Almost everyone has a sibling/friend/cousin under the age of 30 who has had a serious and/or mystery illness.
28. The nicest thing someone did for me when I wasn’t feeling well was: I have three. I can’t pick. 1) My friends Wendy and Kami took me to the doctor and hospital for tests and it was like a 6 hour thing. 2) Kami has been looking up all of these tiny, gluten free desserts and they always brighten my day that she thinks of me (: 3) My friend Michelle insisted that we hang out even despite my gloomy, eeyore-style attempts to dissuade her and we had an awesome day <3
29. I’m involved with Invisible Illness Week because: I am bad at making blogs and would rather do them in survey form.
30. The fact that you read this list makes me feel: appreciated
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
Follow me:
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www.amino.com/emilysstomach
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www.Facebook.com/groups/gpfail
www.Twitter.com/GPfail
www.Twitter.com/fighting4gp
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
Follow me:
www.facebook.com/emilysstomach
www.emilysstomach. o r g
www.twitter.com/emilysstomach
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www.slack.com/emilysstomach
www.amino.com/emilysstomach
www.pinterest.com/chikensrule
www.Facebook.com/groups/gpfail
www.Twitter.com/GPfail
www.Twitter.com/fighting4gp
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
Follow me:
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www.Facebook.com/groups/gpfail
www.Twitter.com/GPfail
www.Twitter.com/fighting4gp
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
Follow me:
www.facebook.com/emilysstomach
www.emilysstomach. o r g
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www.slack.com/emilysstomach
www.amino.com/emilysstomach
www.pinterest.com/chikensrule
www.Facebook.com/groups/gpfail
www.Twitter.com/GPfail
www.Twitter.com/fighting4gp
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http://www.emilysstomach.com/2019/03/weight-gastroparesis.html
#gastroparesisfighter💚 #gp #gpwarriors #gastroparesisfindacure #gastroparesissucks #GastroparesisAwareness #gastroparesisproblems #gastroparesis #GPbattleCry #GPwarCry #gpawareness #gpsupport #gppain #emilysstomach #chronicillness #chronicallyill #autoimmuneillnesses #sickness #sickofbeingsick #lifechangingdiagnosis #noenergy
Follow me:
www.facebook.com/emilysstomach
www.emilysstomach. o r g
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www.slack.com/emilysstomach
www.amino.com/emilysstomach
www.pinterest.com/chikensrule
www.Facebook.com/groups/gpfail
www.Twitter.com/GPfail
www.Twitter.com/fighting4gp
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