In this video I am sharing what alternative nutrition may look like for those with Gastroparesis and Functional GI Motility Disorders. Many in our community are literally starving and dying from complications from these devastating illnesses. Some are able to survive on small "bites" of food throughout the day or liquid only diets, still suffering the pain, nausea, and other relentless symptoms. Others are dependent on Feeding Tubes, IV fluids, and/or TPN to receive the nutrients that they need, but still facing many of the awful symptoms on a daily basis. There are very few treatments available, many of which are unreliable, carry black label warnings due to severe side effects, or not even FDA approved in our country. Please help us raise awareness! We're not invisible. We're tired of our watching our friends and members in our online communities DIE from malnutrition, dehydration, starvation, organ failure, sepsis, etc as a result of the debilitating disease. How can you help? Sign to show your support and ask congressional members to support research and funding for Functional GI Motility Disorders. Donations if interested can be made to IFFGD at https://www.iffgd.org or AGMD at http://www.agmd-gimotility.org/ #TakeABite4GP and share on Social Media Learn more about GP from both the medical and patient side by checking out www.curegp.com
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Trisha BundyA proud mother, educator, Gastroparesis & GI Motility Disorder Advocate, Like my content? Want to thank me with a small token of appreciation? https://www.amazon.com/hz/wishlist/ls/1LH7R639ORBML?ref_=wl_share
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