This topic is about a person who is currently in the hospital dealing with some challenges related to their health and treatment. They have been experiencing nausea, a brief blockage, and a pouch leak, but are now feeling minimal pain and are waiting for a care plan review. Here are some insights and advice shared by others:

1. The person is using a feeding tube for nutrition. An NG (nasogastric) tube ends in the stomach, while an NJ (nasojejunal) tube goes further into the small intestine. The NJ tube has been more stable and hasn't come back up.

2. The feeding tube is for nutritional purposes, not to relieve pressure or contents from the stomach.

3. They have been in the hospital for five weeks and are hopeful about being discharged next week.

4. Eating too much still causes pain, so they are learning to eat smaller meals more frequently.

5. Gaining weight is important before their upcoming surgery, and they are relying on tube feeds to help reach their target weight.

6. Self-advocacy has been crucial, especially when the tube became blocked due to nurses not flushing it properly. It required a difficult procedure in radiology to unblock.

Here are some additional insights and advice from others:

- An NG tube is used to remove stomach contents through the nose, which can be uncomfortable and difficult to insert. Many have found this to be one of their toughest medical experiences.

- The NJ tube, which goes further into the small intestine, is less likely to move out of place or be vomited out.

- It's important to advocate for proper care of the tube, including regular flushing to prevent blockages.

- Recovery should be taken one step at a time, with small improvements being significant.

- Emotional support is vital, and many have offered encouragement, emphasizing the importance of gradual recovery and perseverance.