← Return to Median Arcuate Ligament Syndrome (MALS)
DiscussionMedian Arcuate Ligament Syndrome (MALS)
Digestive Health | Last Active: Oct 29 2:54pm | Replies (1225)Comment receiving replies
Replies to "@lmtuska, Nice to meet you! I have had 2 MALS surgeries done at Mayo, and would..."
Thank you for your posts. I had open MALS procedure January 25/19. Required bypass and graft. 6 days post op, a double sneeze landed me back in e.r. Thankfully, bypass and graft were intact. Discharged to a SNF. I can eat food (yay!) Slow, bland, small amounts. Surgical site is very sensitive, gas pains are intense, back pain is equally intense. I have post op appointment on Monday with Vascular surgeon. I am hoping to get discharged from SNF next week. I think I will feel more comfortable at home. (I must conquer climbing stairs before I can go home) May I ask how long your incision was painful? Did you experience gas pains? Treatment? Which pain medication, other than narcotics worked for you? Any contributors, suggestions, recommendations are greatly appreciated. Much thanks. Be well!
Hi 🙂 please i have a guestin for you i was diagnosed MALS and also a nutcracker syndrome.i will have an open surgery on January 30. So in a few weeks. Wh did you have two surgeries and I year recovery? I am really scared .now are you feeling good ? How many ours did the surgery take ? Thanks for every info
I am having my surgery next week at Mayo can you tell me how long you were in the hospital after yours.
Hi @kariulrich, I was just diagnosed with MALS and I am currently being tested to see if I will need surgery. I am being told I will go to California if it is needed. I also have POTS so flying is tough. I have SIBO and high histamine reactions as well so I have to be real careful with what I eat. I am quite apprehensive about surgery. I wondered if you had the laparoscopic procedure as well? Is there a reason why either or is preferred? I have also heard that some end up needed surgery twice. Was this the case for you and if so, can you share why? Finally, I thought my GI doctor stated there is a 50/50 survival, but I think she meant a 50/50 success rate. I will ask her when I return to see her. I just wondered about anything you could advise to ease my worry. I appreciate the sharing.