excessive gas causes mayo clinic

Some here on the board are not real pleased with the Mayo clinic. It seems they have their own set of standards to give out a dx of MS. I personally know nothing about them and wish you the best....hoping for that answer.

I think that my digestive system got tight and has problems from the SIBO I had last year that was diagnosed by the mayo clinic. The Mayo Clinic says the SIBO is gone, but has most likely left me with these other problems that I am seeking treatment from the Mayo Clinic right now. Hope these new treatments work for me and hope this information might help you.

Has anyone from the MS forum ever seek treatment for their MS at the Mayo Clinic? If so, how was your as your experience with physicians from the clinic? I am considering driving up to Mayo at some point if my neurologist in town can't definatively diagnosis me.

I have just made an appointment for a full work up at the Mayo Clinic, does anyone know the tests involved and how much they charge? Thank you!

I am over the moon excited that DH got a 5-10 day appointment at Mayo Clinic - Dec. 10. Anyone have any experiences on what to expect etc?

Has anybody here been to the neurology clinic at the Mayo or in their inpatient pain treatment program?

What causes gas pain in my left shoulder blade? This discussion is related to <a href="/posts/Digestive-Disorders---Gastroenterology/Pain-in-left-shoulder-blade--left-arm/show/888381">Pain in left shoulder blade, left arm</a>.

Thank you for your response. My husband has been referred to the Mayo Clinic. He is currently undergoing several tests. The possibilities you mentioned are being considered. I feel very confident the medical team at the Mayo Clinic will provide a diagnosis and treatment. Again, thank you for taking the time to answer my post.

Maybe I was too harsh about Mayo. To be fair to Mayo Clinic, I do think they do have some very good doctors there, maybe it's just hard to get a neuro diagnosis - as it seems to be most other places in this country - so what's new? I did really think the Mayo radiologist who looked at my films was excellent - he found a couple of things the original outside radiologist did not notice such as brain mass loss.

I've not been to the Jacksonville Mayo or the MS clinic in Houston, I'm sorry about that. I have heard a lot of good things about the University of Texas Southwestern Medical Center at Dallas and Dr. Elliot Frohman who works there. I'm sure if you google his name you can find out much more than I can tell you about, here.

Truthfully, I've heard one of the best MS Clinics in the US is the Mellen Center at Cleveland Clinic. You might try checking out http://www.mscare.org They list all the clinics available, etc. My neuro said the clinic at Cincinatti isn't that great but thinks Cleveland Clinic is really good. I've never heard of the Mayo Clinic being highly rated for MS, but more for heart desease.

Eventually when I was 16 I was diagnosed with connective tissue disorder and an internal rectal prolapse. They sent me to the mayo clinic and all they had me do was therapy for my prolapse that failed. I progressively have gotten worse and have lost hope on getting help. I have gotten to the point where I have to manually remove stool from my rectum even though it is right near the opening. My body will not allow it to come out.

I am looking into Sanoviv hospital instead of Mayo clinic. I know people personally who have gone there and gotten fixed. One of my close friends has thyroid issues and hep C and went there. She has more energy than a teen. First thing they did was put her on Westhroid and spent 3 days running diagnostic tests. They give you a panel of doctors who all work together in your diagnostics and treatment. I am saving up to go there....

Hello, everyone. I have been "diagnosed" with Chiari via the radiologist that viewed my MRI. I have my first appointment with Mayo tomorrow. The neurologist that originally ordered the MRI had no idea what Chiari was, so I'm trying out Mayo. I am going to the clinic in Jacksonville Florida - have any of you gone? Do you have any experience, good or bad, with them? I have waited SO LONG to get to this appointment.

I decided that I should travel to the United States and hopefully get a diagnosis. I know that Mayo clinic and Cleveland clinic have a good dysautonomia clinics but I don't know which one should I choose so I would appreciate any suggestions !!! Also I know healthcare in the US is so expensive and since I don't have insurance I wonder how much such a visit to one of those hospitals will roughly cost ?I know it's hard to tell but I'm asking for a roughly cost. Thanks.

It mimics IBS and causes a lot of gas pain. If that is the case then you have developed an allergy to gluten and have to change your diet....I am going through testing right now at the Mayo clinic and that was one thing they tested for because my symptoms are very similar. I feel your pain!! Good luck!

when you say excessive gas, do you mean you are passing gas a lot? Or there is pressure? Most ibs causes issues in the lower ab, not upper. Is it causing chest pain? If so, that may be more of an acid reflux type deal, or possibly even both.

Hello and Good morning. I've pulled some information, for yopu, from the Mayo Clinic web site. You are probably aware that the Mayo Clinic is among the best in the world. You can go to their website for more info. I hope that this is helpful to you and your family. I wish you all the best!

Could you have pelvic floor dysfunction? If you do there is a treatment at the mayo clinic for this condition.

Here is an article from the Mayo Clinic on Peripheral Neuropathy. It is a good overview, including causes. The lesion at C3-C4 could well be the cause of the urinary problems. Yes, the urologist has a set of tests that they do, including Urodynamic tests that show how well the bladder fills and emptying and if all the muscles are working in good coordination.

For the last 3-4 weeks I have been having gas problems. First, it started with just normal gas but a little more than usual. Then it became bloating and a little more gas. Now, it has turned into excessive gas that has been quite frequent and to mention embarrassing. I usually don't know when I will pass gas. I have involuntary gas and voluntary gas. I don't know when the involuntary gas will occur. It always feels like my anus is open.

I am a 27 year old male. I have had extreme excessive gas for a few months now. It is usually worst at night, maybe because of eating dinner, but not sure. It does not seem to matter at all what I eat, it happens every night. I am amazed at the amount of gas I have, it just keeps coming, I can feel it building up inside me and after I expel it it just happens again.

m going to assume you have this excessive gas and have no idea why or what to do about it. Here is what I would suggest you do (in this order)...1. Make sure your eating a healthy diet. Lots of whole grains, fresh vegetables, fruits, nuts, etc. 2. Make sure your bowels are moving regularly. That means you should have 1 large bowel movement every single day (some doctors say you don't need to have a bowel movement every day BUT THEY ARE WRONG!) 3. Take a probiotic. Try Activia.

Can anyone assist share with me how to deal with excessive gas, I am very mindful of my diet and has recently started to exercise. My periods are no longer painful since starting the pill, however from first day of bleeding the gas pains are so severe that standing upright is excruciating Any help or advice? Please, anyone?!?

Excessive gas causes mayo clinic

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