actonel side effects 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.

After recovering from Stage 4 Kidney Failure, after 4 years off Simvastatin, which caused it, my doctor recommended an MRI with and without contrast. I objected to the contrast dye because I knew about the risk of NSF (Nephrogenic Systemic Fibrosis). He assured me that my kidneys would flush it out of my system in 24 - 36 hours. 4 days later I awoke with both hands clenched tight and opening them was painful.

and this is to help keep nasal membranes moist as well. An ENT doctor at Mayo Clinic told me to use this as well, even though I have Vasomotor rhinitis. Hope this is of some help to you I would go and see an ENT doctor though. and be honest with him about your past use of cocaine., as this could help with your treatment of your nasal problems.

I am already looking into takeing him to the mayo clinic, where we are the choices are limied but I will keep in contact.

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?

Thank you so much for taking the time to respond, it is greatly appreciated. My last vaccine was over a week ago, and I have seen some fluctuation of the side effects since this post as well. They are fairly steady and constant, but I have noticed a decrease on occasion so am hopeful they may all pass soon. I’ve also began utilizing OTC pain meds daily which do help tremendously the constant headache.

Is there something that I can do to combat the yucky side effects? Also, what about surgery? I do have a Dr. at Mayo that suggests a consult with the Neurosurgeon. I'd appreciate any feedback or ideas... Thanks much!

I have been at the Mayo Clinic for the last week. It has been a very pleasant experience, given my circumstances. They have been very efficient and very informative. They have treated me like a person and not just a number. I am very impressed. I am looking for some personal advice on medications. I was dx with CIS due to the fact that I am not really experiencing any symptoms other than the optic neuritis, which has resolved for the most part.

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.

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.

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.

The best place to find side effects of a med are to Google a reputable source like Mayo Clinic or read the package insert you got since it is where mayo would get their info. Anyone who tells you they have a side effect that isn't listed on the label is just giving personal anecdotal evidence which might be just in their imagination.

s side effects, such as the one from the Mayo Clinic, if you want to research the drug on the Internet.

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.

) Unfortunately, Reglan is notorious for its side effects. If these are too much for you (and they sound like they are), ask the doctor to switch you to Domperidone. The drug is NOT available in the US, but is first-line treatment for GP pretty much all over the world. You can find Canadian pharmacies which sell to the US (prescription required) through PharmacyChecker.com, which is recommended by the AARP.

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.

Since then I have been on various rounds of antibiotics, prednisone, cough syrups, singular, symbicort, albuterol etc. I had been treated at the allergy clinic years before for allergies and asthma. I have had to take about 8 days of 10mg prednisone about 4 -5 times in the last 8 months. It is about the only thing that helps my coughing and spitting up of phlegm.

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.

I'm sorry, you're probably going to wonder why I'm even responding to your question. I have had chronic pain for the last two years and have had one diagnosis after another. Neuropathy has been one of them. I so feel your pain (literally). Make sure you have a good doctor, get more than one opinion and don't just let them try to give you a bunch of pills unless they know FOR SURE what is going on.

I have advanced tardive dystonia. The two I went to in the past that were the most helpful were the movement disorders clinics at Mount Sinai Hospital and Columbia University Hospital which are in the New York area. However there are many movement disorder clinics around the country that have trained movement disorders specialists who should be familiar with treating tardive dyskinesia.

10) Sadly, he still feels that I have enough neurological symptoms that had not been addressed properly and continue despite all that has been done for me, so he referred me to the Mayo Clinic. Specifically, he thinks I have MS, so I will start in neurology. Now, you are caught up! BTW no Hashimoto's-never had a positive antibody test result. Thought at one time to have Hashimoto's encephalitis, fortunately that was a no.

The severity of the difference would also be dependant on the length of your Herceptin treatment. Oncologists monitor these side effects very closely and I'm sure your Onc. will take this into consideration and discuss the risks of continuing your treatment. The longer the treatment the less the incidence of heart damage but each case is different. Regards ....

Actonel side effects mayo clinic

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