Connect
← Return to Mesenteric Panniculitis or Sclerosing Mesenteritis
Discussion
Mesenteric Panniculitis or Sclerosing Mesenteritis
Digestive Health | Last Active: Nov 6 8:25am | Replies (1517)Comment receiving replies
I met with the GI doctor. He said he did not think my lower abdominal pain was related to MP - his experience was that MP takes a long time to manifest (for people with MP pain). My CT was not with contrast, so he has suggested trying Mirolax first to rule out constipation and if that doesnt work he will have a contrast CT done. Since I started CBD I am having no night pain - I found it hard to believe so I didnt take any last night to see if pain was still even there, and it definitely was. Maybe its enough of a relaxation to stop any cramping.
Replies to "I met with the GI doctor. He said he did not think my lower abdominal pain..."
My MP, we don't think took a long time to manifest itself. Two weeks to the day of my fall, was when I started feeling the symptoms. I had tried CBD, but it didn't seem to make a difference. Maybe, I should give it another shot?
I had inguinal and umbilical hernia surgeries prior to my MP diagnosis.
Have had 3 large painful boils on my upper groin/stomach area afterwards
too....not sure if that is related.
I use to smoke MJ all the time, it's the only thing that would help me with my back pain, now I have MP and I can't really smoke anymore, the THC helped a lot and also with depression from being injerd, I did try to smoke with MP and I felt happy but bloated from my stomach and had a hard time burping 😔 so now i might try edibles to see how thR helps
Wish you my best 🙏
Connect
Well isn’t that interesting. A little bit like my GI doctor said. I had my CAT scan with contrast. That’s why he said my pain was related to IBS not MP.....I should try CBD....I am 78 and need to get my head around the CBD. Lol! I will see if my daughter can get it for me. Keep me posted pls. I will let you know if I try the CBD!