Brunner's gland hyperplasia
Brunner's gland hyperplasia symptoms and treament
Interested in more discussions like this? Go to the Digestive Health Support Group.
Brunner's gland hyperplasia symptoms and treament
Interested in more discussions like this? Go to the Digestive Health Support Group.
I have been telling Dr's since March that I am bleeding and still continue with it! The camera showed multiple places of bleeding.
After my hospital in March, I was assigned a different GI Dr. It took 4 months (July) to get in to see their NP.
I have told all my Dr's I have not had a good bowel movement since March. I had to do the prep for the camera and ended up on the same day as camera appt. back to the hospital because I knew I was bleeding. Confirmed be hosp. Dr. Luckily the ER doc talked to the GI Dr. that was supposed to do the camera on Monday to please do it on Tues. The schedule that this Camera Dr. is Monday, Wed, and Fri. By Monday I had not really eaten since Sat. Prep started Sunday. Today is Sunday, camera still there! Put in Tues. Thanks
Thanks for sharing your story!! I have acid reflux and my gallbladder removed years ago!!
I hope you can get good results! I believe that Dr.s sometimes ignore our symptoms because they don't know enough about our disease and symptoms!
Prayers for you!
I was diagnosed with BGH years ago! My Dr. at the time found it on an endoscopy! At that time her told me not to worry about it, nothing will happen. He has since died a few yrs ago and no one in the medical community here in Louisville seems to specialize in it!
I have googled BGH for answers thru the US and know one comes up.
I am comforted, @hhd to see you find this discussion so you can connect with others dealing with Brunner’s Gland Hyperplasia. I am glad you found this discussion related to the camera and bleeding you are currently dealing with. https://connect.mayoclinic.org/discussion/pillcam/
I am tagging @xmipou, @tryingrealhard, @amandaa and @clementels to learn what updates they may have.
An appointment at Mayo Clinic would be a good option for you to check out: http://mayocl.in/1mtmR63
How are you feeling?
Looking for information or guidance. We have a 9yo boy that has had stomach pain for 4 months. He describes it as pressure right at the belly button. His symptoms include: pressure, nausea, loss of appetite, constipation.
The symptoms are present everyday but do flare causing symptoms to be worse. The flares can happen at anytime but definitely after eating & car rides.
When doing a endoscopy BGH was found. We are trying to find the root cause of these glands to be hyperactive and so far have only managed to wrack up thousands of dollars in medical bills & our sweet 9 year old is still in pain everyday.
A little background: in March he was diagnosed with a histamine disorder, we chose to use supreme nutrition herbs to aid in gut healing. Since he was a baby he has never had a normal stool and has battled with skid marks his entire life. He’s struggled with rashes around his mouth, on his elbows & knees. He often get stye’s in his eyes & canker sores. He also has tics, some are verbal & some non verbal. Along with chronic congestion.
In March we pulled gluten & dairy from his diet & the rashes, chronic congestion, styes, canker sores & tics have since improved. The end of April is when his stomach pain began and he went from pooping daily to constipated. However, looking at the skid marks we wonder if he’s been chronically constipated his entire life and since removed his trigger foods his body is now relearning how to have a normal bowel movement. But how does the Brunner Gland Hyperplasia fit in? What could be the root cause? Is this all apart of the healing process or is there an underlying condition and if so, where do we go from here? From a GI standpoint BGH is a normal finding but all my research shows is actually rare & typically a response to something else going on. We are desperate to help our boy and are hoping this might bring some light and help us find him some relief.
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1 ReactionHi @healdm01, and welcome to Mayo Clinic Connect! The last 4 months must feel like a nightmare.
I am not familiar with Brunner Gland Hyperplasia, but want to invite @tryingrealhard, @custom1222, @xmipou, @clementels, and @hhd who have discussed BGH.
You mention a GI doctor, and also a histamine disorder. Has your son seen other doctors, and if so are they working together to figure out what is happening? What led to his histamine disorder diagnosis?
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2 ReactionsThank you for the reply! My 1.5 year old was diagnosed back in December, he was born with a group of histamine cells we thought were a birth mark. After his diagnosis and research we realized this was likely a genetic factor and myself and all 3 kids were eventually diagnosed. Right now are are just working with GI. We did request an appointment with Mayo and they denied it. So I’m reaching all platforms to hopefully find some light and direction on where we go from here. I won’t give up until I find someone willing to help us. But first I need all the research and experiences with BGH to help me better understand what could potentially be the cause. The Mayo put our request in with some other departments and I have been in contact with a couple GI doctors at the U of M than mentioned Rheumatology & Immunology next but I’m trying so hard to also protect him because every appointment leads to more blood draws and it’s driving his anxiety. BGH seems rare and I feel so alone and so unheard. Any feedback here would be so appreciated.
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2 ReactionsHi, @healdm01 - I wanted to let you know that I moved your post here to an existing Mayo Clinic Connect discussion on Brunner's Gland Hyperplasia.
Glad you got connected with @jlharsh. I'd also like for you to meet @lakelady55 @hhd and others here. Hoping they can shed some light onto any condition that may be underlying the BGH.
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1 ReactionThank you!!
Thank you so much!! i truly appreciate it!