hysterectomy recovery mayo clinic

So far they wont do anything for it now I changed hospitals to mayo clinic and hopefully they will remove the cysts. Its possible tho I could have a third one. I took a year off of the hrt to find out the cyst still grew without hormones. So they don't think the cyst is due to HRT. Any clue to why this happens? I have never had endometriosis. When they aspirated it before it showed lactobacillus,which comes from the intestines as far as I know; in the lab results.

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?

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.

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

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.

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.

There are many reasons for an elevated CA125, but to get definitive answers, even consider contacting either the Mayo Clinic, or Cancer Centers of America.

We just returned from the Mayo Clinic in Rochester, MN and had a horrible experience, from start to finish. I was wondering who else has had such a bad experience as we did? To summarize, my wife has an upper spinal lesion (C1-C3) and almost died 3 yrs ago. The lesion is tumor-like but has not yet been diagnosed as to the cause to this day. Prior to the spinal lesion being diagnosed, she had been sick on and off every year for the prior 10 yrs.

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.

t hear back from them right away - I requested an appointment with the Mayo Clinic and it was almost a year before I heard back from them! If your current docs office does the request/referral, though, it should go a lot faster.

I need to have a minor outpatient proc but am horrified due to my complications in recovery from cryo. Is it ok to go under anesthesia? I tried to go to Cleveland Clinic or Mayo Clinic for another eval but ins. Wouldn't approve referral. My nerves are shot. Please help!

Cleveland Clinic and Mayo Clinic are obviously both top-flight medical centers, so the choice between the two would not be so much "which is better, Cleveland or Mayo;" it would be which one has a doctor or program that is more specialized to what you need.

A while back I entered the patient scholarship opportunity for the Social Media conference at Mayo Clinic. You may have even been one of the many people who ‘liked’ me through Facebook. They awarded three scholarships for the patient/caregiver and one companion to attend the conference. I was not one of the three people selected to attend, but I did reach out to the winners with my congratulations.

I just read that the Mayo Clinic in Arizonia is denying medicaid patients due to low reimbursments. They have to pay cash. Any thoughts?

I went to the Mayo Clinic in AZ in January - hoping to find some answers. I will say that it is a very well run facility - but don't pin your hopes on a big "well known" facility to solve everything for you. The neurologist that I saw at the Mayo clinic didn't want to see my timeline or my list of symptoms - although at the end of my initial appointment, he did take my list of symptoms to include in my chart.

My doctor suggested that I have the rectocele surgery repair. I'm hesitating because I've heard horror stories about the recovery and pain afterwards (from other posting sites and my Mom as well who had the surgery 15 years ago). I've been navigating this site and it seems like people here are not spreading fear. Just how bad was the surgery and post op? Thanks.

He also had quadruple bypass surgery and a reaction to statin drugs. Mayo clinic in Rochester was where he went for a second opinion. I highly suggest going to the top (Mayo) if you can travel. Our hospital here was tellling him it was his heart and he needed a defribulator. Mayo found out his heart was perfectly fine and it was his lungs. Get a second opinon.

Has anyone responded to your question? I was recently diagnosed and heard that Dr. Gray at the Mayo Clinic does have some expertise in treating this disease. Of course, my insurance does not cover the doctors at the Mayo Clinic. I have been seen at the UCLA Revlon Center, but they really have no expertise in this area, so I feel like my treatment has come to a standstill.

DO not go to Mayo ? I repeat do not go to Mayo clinic , they trun away people with Chiari . There are other experts al over the US . where do you live ?? TRY EMAILING ME remmel50 (THE AT SIGN) netins.

My new neuro wants to refer me to Mayo Clinic. She thinks this is definitely an autoimmune disease but doesn't think that it is MS due to the intermittent low grade fevers for no apparent reason. I haven't discounted the fact that more than one thing may be going on. Anyway, saw that JH has the big autoimmune disorder research center and wondered, if this is what we're looking at, if it might be the better place to go. Any comments??? Thanks!

You can go online and register or call to set up appointments at Cleveland Clinic and the MAYO Clinic. MAYO has three clinics in the U.S. You do not need a referral to get in to either of these clinics. I have also heard of people the drive there and tell them their symptoms and sometimes they get in right away. So, you might want to consider checking them out online and trying to set up an appointment. I hope this will help you, as I know how frustrating this can be and disabilitating.

It takes several weeks for your body to heal after a hysterectomy so it's best to follow the Drs orders. Take things slow and get plenty of rest.

m curious as to why so many people are against the Mayo Clinic? I myself am a patient there currently undergoing diagnostics, though I received a clinical MS diagnosis upon first appointment in November, at this time my other cranial issues and viral issues are also being examined. My Neuro there was able to detect issues in one visit that other facilities could not in several other states- including Stanford Over the course off seven years.

Hysterectomy recovery mayo clinic

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