NORCALRN

i hear ya. i went from NG to plus PICC to NJ to get strong (7 weeks in hospital) but 31 days with Nasojejunum tube...then another semi perm jejunum tube for about.14 months on off. i pulled out the NG tube cuz it sucked. its easy to do....I am wishing you the best. long road ahead but remember how strong you are and utilize your support system. All self preservation goes out the door after what we have gone through. Plus, I am a nurse so I see both sides now. get better... t

yes, thoracenteces will make you feel better as well as antibiotics, I had major complications and the first time in the ER draining my lungs I felt nothing, but later in the hospital, it hurt, plus I had hospital acquired pneumonia so drains went in. Thank you for sharing your experience as it reminds us that we know our bodies better than anyone and we should speak up. I hope your recovery is uneventful!

I struggled,too. I hear your frustration and pain. My ordeal was just over 3 years ago and i spent about 7 weeks in the hospital and on/off J tube for 14 months. What I can tell you is just keep speaking to your health care team and push for other meds, etc that you think might help after you have researched everything. Go through my threads if you are up to it. I still take Protonix twice a day as well at Zofran 8 mg twice per day. My appetite is better and now I can start improving my stamina for cardio and get my weight loss moving again. I guess I just want you to know that it really does get better. I was soooo tired of hearing that - but it is the truth. In the end, this will be behind you and your focus on physical and mental recuperation will begin. Please, let family or friends help you out. You will appreciate it and it will allow you to get the rest you need. I hope to see you updates. This is a great forum so reach out to us......you are not alone that is for sure. This group helped me a lot. I am a nurse but it did not matter - what we all need is support. Get better -check in and rest! Trish

It sounds like you are on the right track regarding the allergy component. There is another med instead of Zofran. It is Anzamet but it is on backorder (no generic yet). For me, it is less sedating than 4mg or 8mg Zofran. I still am suffering from stomach issues 3 years out, but it is getting better I guess. Since Flonase is not systemic, it is less drying to your nasal passages so I would make sure you take that. I hope you feel better!

Mine was no help but I ended up with a J tube so for the most part, i did not need her.

I had an EKG, labs only upon preparing for surgery upstairs. and the doctor assumed my personal report on my health was correct (which it was) but no labs, etc. Dr. Almanza - 2012 did my sleeve.Oh - I did not even get weighed! I went first out of the 8 of us because I was the smallest (needed to lose 65#). He took his last patient in at midnight and he started with me I think around 1pm.

no....I do not eat much anyway, especially as the day goes on. I cannot say I have overeaten...it is not possible for me to get that much solid food in. i still utilize liquids mostly. egg whites in the morning. I concur with a previous member's post about the terrible feeling of food being stuck in the esophagus....it just sits there until I vomit. I see my GI MD next week and I am just 3 years out (7-27-12). sometimes I will try a solid and it stays down but hurts and I am always nauseous - the next time I try that same food, I vomit. I never know. I pretty much do not try to eat in public.

It is the clear mucous-like spit or "slime" that likely remains n the stomach..it lines it to prevent acid irritation, assist in digestion, etc. It happened to me for bout 2 plus years and still occurs. vomiting often goes along with it. Sannah - I know what you mean in your post. eat like you should, but watch out cuz here it comes right back up!!!! SLIME good for the stomach, but bad in excess....not fun at all!

Hi Sannah beautiful children!! I think your original picture had a banana phone - right??!!! I can completely understand when you say that you feel that you should be able to do more, help out, live a better life....I am in and out of bed for days and cannot work much ( RN, BSN). Just had more labs done today. So sick and tired of being tired!!!! Nausea is unrelentless and I finished my antibiotics for the H. Pylori and within 2 days, pain again so they think that was not really the problem although it did help with epigastric pain so maybe the ulcers are better. I just know that something is wrong. I see a therapist like you, and I am grateful for that. I guess I just wanted to reach out to you and let you know that others care and want you to get better! trish

i live in Novato......would be interested!

oh Sannah I wish I could make it better for you. My quality of life has been changed forever, too.Work (RN, BSN), money issues depression. I am sure you are familiar with all of it. Your last post made me so sad....I hope you are not alone...you have a child i think? keep reaching out - here, family, friends wherever. I know that I will never be the same physically and will always be monitored for malnutrition I do not want a j tube ever again). Chronic fatigue, not knowing if you are gonna throw up, gastroparesis, cyclic vomiting syndrome...sheesh. BUT, we need to keep going. get up and do what we need to do for ourselves! So, I am here for you as well as other I am sure. The post from Kathy (proudgrammy) is full of wisdom. you just get through this one minute at at time....take it in, breath and start again. trish (that one is me pre-barf period)!!!!heehhee

I would keep trying different brands. Most places such as GNC will let you exchange it if you need to. I still use crushed ice in mine. I have to have things I drink really cold, or I gag. And yes, sometimes it creates a spasam due to the cold. But really, keep buying new ones. unjury seems popular. hang in there......it does get better!

not really, even with my ongoing complications. regret is something i do not want to feel. moving on, working on health, I only had 65# to lose and went to Mexico..but that is not why i had such serious issues - so if you or someone is contemplating..go for it. If you have diabetes, high bp, etc, this surgery may save you in so many ways down the road. do your research, feel confident about your choice......it is all up to you!

oh my......it never seems to end. i still feel liike there is something else beside h. pylori and ulcer.......labs are ok. they ususally are.even when i had a nasojejunum tube then the j tube. very little showed except i looked like sh*t and felt worse! i am so weak....not depressed weak - just wiped out. and try getting giant antibiotics down..holy moly! anyway, i am going to see an option to reach out to you outside of this forum. stay tuned! trish

hi Sannah I just posted an update (somewhere)! I hope you are doing better. This sucks I know. Life on hold AGAIN. Miserable is a good way to describe how I feel, too. But we are strong and can handle this. See if you can find my recent post - literally just a minute ago I updated. keep posting- we all want you better! Trish