Medical
$0 raised of $18,600 goal
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Child's diagnosis short bowel syndrome
by Brandon
Created Mar 19, 2022 |
California
- 0 Donations
- No deadline
- 5 Likes
Child's diagnosis short bowel syndrome Short bowel syndrome (SBS) is a set of symptoms caused by an increase in the functional activity of the surface of the small intestine as a result of intestinal resection, manifested by chronic intestinal failure and leading to a violation of the activity of the body as a whole. From the point of view of modern consciousness, SBS is a violation of the function of the entire intestine, since the presence or absence of the large intestine in conditions of shortening of the small intestine plays a significant role in assessing the prognosis and outcomes of diseases.
Purpose of fundraising Numeta nutrition course for 6 months Child's story Everything that happens in the life of little Veronica can only be called a miracle. In the first month of her life, the girl underwent three most complicated operations to save Veronika's life, the doctors discovered that almost the entire small intestine had been removed. At the same time, ordinary food is not digested, and for life and movement, the girl needed parenteral (intravenous) nutrition.
The dream of Veronica's parents is for their daughter to survive over time from internal infusions and eat and grow up like ordinary children. Doctors believe that this is possible - but the process of restoration (lengthening, growth) of the intestine is lengthy, there can be no quick solutions. Right now, Veronica needs special nutrition, which gives the body resources for growth and development.
For all the time, an operation was performed to replace the central venous catheter. The operation was successful, Veronica quickly recovered. Over the past six months since the last visit, she has grown well, and doctors believe that two days a week she can do without droppers. If she continues to grow well and gain weight, gradually the number of droppers can be reduced. The body needs to learn and adapt. All this time, you need to receive a power measuring device. Therefore, we again ask for help and believe that Veronica will overcome the disease! We are immensely grateful to everyone who helps us in the fight for the life of a child!
Purpose of fundraising Numeta nutrition course for 6 months Child's story Everything that happens in the life of little Veronica can only be called a miracle. In the first month of her life, the girl underwent three most complicated operations to save Veronika's life, the doctors discovered that almost the entire small intestine had been removed. At the same time, ordinary food is not digested, and for life and movement, the girl needed parenteral (intravenous) nutrition.
The dream of Veronica's parents is for their daughter to survive over time from internal infusions and eat and grow up like ordinary children. Doctors believe that this is possible - but the process of restoration (lengthening, growth) of the intestine is lengthy, there can be no quick solutions. Right now, Veronica needs special nutrition, which gives the body resources for growth and development.
For all the time, an operation was performed to replace the central venous catheter. The operation was successful, Veronica quickly recovered. Over the past six months since the last visit, she has grown well, and doctors believe that two days a week she can do without droppers. If she continues to grow well and gain weight, gradually the number of droppers can be reduced. The body needs to learn and adapt. All this time, you need to receive a power measuring device. Therefore, we again ask for help and believe that Veronica will overcome the disease! We are immensely grateful to everyone who helps us in the fight for the life of a child!
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