Stomach pain and throwing up repeatedly
My 11 year old son has that had stomach pains and has been throwing up for a month and the doctors just want to keep giving him meds they've done CT scans x-rays MRIs and still no idea what is going on he throws at 4 to 6 times a day he hasn't lost weight and has no fever and I'm very frustrated that he has missed almost a month of school because of this cuz he can hardly move cuz it stomach hurts
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I'm VERY sorry for your experiences! My husband has gastroparesis and has also developed depression, anxiety and fibromyalgia. He experiences many of your symptoms. He, too, has difficulty at times, trying to face a life in which he has so few truly enjoyable days (and our definition of "enjoyable" has immensely changed). I don't have any answers, but pray you will be able to hold onto faith and hope and that you have family to support you! My husband was prescribed a pain patch instead of taking oral pain meds. The patch seems to provide better round the clock pain control without the highs and lows associated with taking pills. Also, there is less chance of abuse with a patch than will pills. Have you considered a mask and gloves during this pandemic to facilitate your travel to the Mayo? Everyone's comfort level with COVID-19 is different. If you feel you could safely travel, I highly recommend the Mayo. We got nowhere with my husbands problems until we obtained Mayo care. They are amazing!
Yes, it’s not a good quality of life. I’m hoping the test I’m having Wednesday will find the cause. We have narrowed it down by process of elimination. I am not concerned about catching Covid, it just makes things more difficult. The mask makes me sweat which makes my stomach hurt worse. I don’t think gloves really do anything anyway. As long as you keep hands clean and not touch your face your better off without Gloves. Once we get the results from the vascular Dr we’ll see if we need to go to Mayo. This is pretty much the last thing it can be.
Thanks. I'm praying so hard that this is what it is. We are out of options and I cannot continue to live like this.
@trip17 - Good luck with your appointment tomorrow!
As I read your last post, it struck me that I used the same words as you do - I can’t continue to live like this- when MALS diagnosis was made and I decided to go through surgery.
How bad was the surgery?
@trip17 - The surgery was okay. Laparoscopic, pain not bad. After surgery I had spasms of the diaphragm because the ligament was attached there. However, with gabapentin this nerve pain was very tolerable. No regrets!
How long was recovery?
@trip17 - the severe pain was gone immediately. The post-op pain lasted about 2 wee
HI . My wife had similar pains . But no bledder removal. Once all tests were OK - Our doctor suspected that it can be something connected with her nerves. We had a meeting with a nerve specialist . He agreed with our doctor and recommended to start to take CLONEX . It was a real miracle after a few hours the pain diasppered. She took a few days a strong dose of 2 mg and then 3 times a day a 1/4 of 0/5 mg.
Thank You! I will look into that! We are down to it being either a ligament that is squeezing an artery or a nerve issue. I took a test for the Ligament artery (called MALS) a couple days ago but have not heard anything. If that's not it, it has to be a nerve, but I'm heading to UT Southwestern Diagnostic to let them try to figure it out. I want to go to Mayo in Jacksonville, but don't think my insurance will cover it.