GI Nodes Eli5
Does anyone have a resource that shows all the crazy GI nodal volumes. Its always been a knowledge gap bc I dont think I ever got taught it well, and it seems like everyone always knows these. Theres perigastric, celiac, splenic, portal, suprapancreatic, pericholedocal, gastrojejunal/hepatojejunal/pancjejunal. How in the world do you remember what to cover when. Like wtf, just treat 3D and be done with it. Anyway, need to know it for the boards
Also, can I get an ELI5 (explain to me like Im...
GI Nodes Eli5 (Source: Student Doctor Network)
Source: Student Doctor Network - May 13, 2016 Category: Universities & Medical Training Authors: Haybrant Source Type: forums
Coeliac disease
Forum: Army Jobs – Ask the Army
Posted By: Adores
Post Time: 17-04-2016 at 01:47 (Source: The Student Room)
Source: The Student Room - April 17, 2016 Category: Universities & Medical Training Source Type: forums
Re: Recognition, assessment, and management of coeliac disease: summary of updated NICE guidance
(Source: BMJ Comments)
Source: BMJ Comments - November 1, 2015 Category: Journals (General) Source Type: forums
Re: Celiac disease and non-celiac gluten sensitivity
(Source: BMJ Comments)
Source: BMJ Comments - October 17, 2015 Category: Journals (General) Source Type: forums
So confused....no diagnosis...stop looking?
Looking for confirmation my 8 year old daughter doesn't have cf. Wondering what is going on. Has environmental allergies (as shown on skin tests 2x). Diagnosed with asthma 2 yrs ago due to cough...no wheeze ever. Last school year had bacterial pneumonia in Sept (x-ray at er) and bacterial pneumonia in May (2 night hosp stay). Possible pneumonia in mid June...treated but no x-ray. In past has seen GI for possible reflux and genetics b/c she didn't sweat. Sweating has slowly started and they think possible connective tissue disorder.
Recurrent pneumonias have lead to numerous tests. She's been doing really well sinc...
Source: Cystic Fibrosis Newly Diagnosed Forum - September 24, 2015 Category: Respiratory Medicine Authors: mom2girls Tags: Newly Diagnosed Source Type: forums
Fibrosis in the stomach lining.
Can anyone give me any insight on whether fibrosis found in stomach lining is DEFINITELY CF or not?
My daughter's GI did a scope and biopsy last Friday and received the results today. She said they found "fibrosis in the stomach lining" and she would have to do further research to find out what that meant. I, of course, could not stop myself from googling and over and over found my queries leading to CF. They also found reactive changes of the esophagus. She is 19 months old with IgG-deficiency, they were doing the scope to look for evidence of celiac's. She has been chronically constipated since we switched fr...
Source: Cystic Fibrosis Families Forum - July 30, 2015 Category: Respiratory Medicine Authors: twinmomIM13 Tags: Families Source Type: forums
Celiac disease - what is your experience?
Forum: Health
Posted By: czechmishaout
Post Time: 09-03-2015 at 11:03 (Source: The Student Room)
Source: The Student Room - March 9, 2015 Category: Universities & Medical Training Source Type: forums
Weight and BMI before feeding tube?
Okay, so I am trying to find out from CF folks what was your BMI and weight prior to getting a feeding tube and did you gain weight after placement and if so how much? I've lost quite a bit of weight since my Celiacs diagnosis and I was concerned cause my BMI is 19.32 right now and I weight 110lbs. I also can't have dairy products or anything with soy protein cause I have cross-reactivity issues due to the Celiac so this makes gaining weight difficult. I know, eat avocados, peanut butter (which I hate), nuts, olive oil, ect. but there's only so much of that stuff you can eat and I'm starting to feel completely uninterested...
Source: Cystic Fibrosis Nutrition Forum - December 27, 2014 Category: Nutrition Authors: RobinB29 Tags: Nutrition Source Type: forums
DNA results
Well my daughter had the fecal elase (not sure on spelling, sorry) testing done, doctor at CF clinic said it came back fine, no loss of pancreatic function, so relieved!! She also had blood drawn for the Ambry full screen. We waited a little over a month till the doctor called with results. He said given her negative sweat tests and only the one known disease causing mutation he is considering her just a carrier. I was so relieved with this news I didn't think to ask what the actual results were! I called the CF clinic asking if they could fax the results of both tests to me & the receptionist stated she would have to ...
Source: Cystic Fibrosis DNA and Mutations Forum - December 11, 2014 Category: Respiratory Medicine Authors: Makmomma2 Tags: DNA and Mutations Source Type: forums
Could I have CF?
I've had what has been diagnosed as horrible allergies my entire life. My nose is completely clogged 365 days a year, to the point where I basically can't breathe through it. What's worse is I have this horrible post nasal drip. It's so thick and copious that I feel like I am constantly choking. I'm coughing and sniffling literally every second of every day. Although I do exercise, I have a hard time breathing when I run. I often feel like I can't breathe deeply enough. I feel like I constantly have a sinus infection, I've had probably 2-3 a year for as long as I can remember. I've had my lung capacity tested before to see...
Source: Cystic Fibrosis Newly Diagnosed Forum - October 30, 2014 Category: Respiratory Medicine Authors: Lannister Tags: Newly Diagnosed Source Type: forums
Coeliac/Gluten Free Friendly Oxbridge Colleges?
Forum: Applications and UCAS
Posted By: Maxomatosis
Post Time: 17-09-2013 at 09:47 (Source: The Student Room)
Source: The Student Room - September 17, 2013 Category: Universities & Medical Training Source Type: forums
