Dandruff mayo clinic

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dandruff

627388 tn?1222198212 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.
Avatar f tn 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!
582396 tn?1259863489 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?
Avatar m tn 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.
1264955 tn?1381782221 Has anybody here been to the neurology clinic at the Mayo or in their inpatient pain treatment program?
486038 tn?1300063367 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.
Avatar m tn 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.
Avatar f tn And when the bottle says lather rinse repeat actually repeat. Lol. For dry scalp dandruff you canuse mayo on your hair coat scalp and hhair leave on for 15 min rinse off. Or 3tbsp olive oil one egg and I think it was a tbsp of vinegar and put that on your hair leave on for 15 and rinse. These are easy recipes you can find online.
Avatar f tn 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.
Avatar f tn 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.
655875 tn?1295695107 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.
553283 tn?1409694311 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.
572651 tn?1530999357 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.
973741 tn?1342342773 I just read that the Mayo Clinic in Arizonia is denying medicaid patients due to low reimbursments. They have to pay cash. Any thoughts?
237053 tn?1258828426 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.
Avatar f tn 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!
Avatar n tn after using any anti dandruff shampoo like clinic plus, head & shoulder my head ache starts. why? i use other shampoo also but only anti dandruff starts my head ache. i want to know which chemical affecting me?
Avatar f tn 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.
Avatar f tn 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.
1166523 tn?1264364643 I will be going to the Mayo Clinic if FL to their MS specialist to confirm or deny MS in Feb. I am very excited about , hopefully, getting some answers. Has anyone here been to the Mayo Clinic? I was wondering what to expect and if anyone knew anything about Dr. Sheuster (sp?). I will be seeing her. Thanks!
Avatar f tn I have POTS and am supposed to go to the Mayo Clinic in Minnesota this winter. I'm curious who has been to Mayo before and how their experiences went. Did you use the POTS clinic part of it or something else? I am also curious because I am mainly going to see if any doctor can figure out the underlying cause of my POTS (my current doctors are not interested in testing for any possible causes of it). Should I go to the POTS clinic part of it or should I just see a general doctor there?
Avatar f tn 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.
1166523 tn?1264364643 Hi janereed, I went to the Mayo Clinic in Rochester, MN in Oct 09. When I first walked in it was a dr that was training to be a consulting dr and he told me that they believed I had a stroke and that I was gonna stay like I was without improving. Well I blew up at him because he hadn't even examined me or anything. And all my other dr's from home had ruled out a stroke and said MS. Well the consulting dr. (Dr. Keegan) came in and did an examination and was very nice.
228463 tn?1216761521 I have been referred to see another team of neurologists at the Cleveland clinic in Weston since my doctor thinks the Mayo clinic did not do the proper workup that the $15K should have paid for! I would appreciate anyone's take on this clinic - am nervous about starting another series of tests that may bring me to "post viral syndrome dx" again with more time and money down the drain. Hugs to all!