depression treatment michigan

I am in Western Michigan and there is really nothing here. I do have University of Michigan in Ann Arbor or Henry Ford Hospital in Detroit. Does anyone have any suggestions in Michigan or should I go to Mayo? I read that someone in Michigan went to someone in Grand Rapids and the doctor required the patient to commit to treatment with him before he would do a liver biospy....thats not acceptable to me...what if you do not like this doctor or the staff?

failed to use corrosion control treatment and/or refused to mandate the treatment once dangerous lead levels were detected and manipulated; and he manipulated water samples by telling residents to "pre-flush" their taps the night before their samples were drawn and/or failed to collect required samples and/or removed results from samples slated to be included in the 2015 report.

http://www.newnownext.com/michigan-house-passed-bill-allowing-emts-to-refuse-treatment-to-gay-people/12/2014/? "Over the weekend, Republicans in the Michigan Statehouse passed a “license to discriminate” bill that would give just about anyone the right to refuse service to LGBT people if it conflicted with their religious beliefs.

I live in Michigan and see we have the gamma knife at Mid-Michigan Neurology. I take several drugs to help with the pain, but it's never gone entirely. I'm willing to travel to seek treatment.

All you can do is to mention they are doing a trial treatment at Henry Ford Hospital ( the one on Grand Blvd ) and the treatment is free--no cost to him at all. If he wants to enter, he must do it quickly for they will be starting in a few weeks. He can call the number I gave in the first post. Has he had a biopsy? Do you know what stage and grade he is? Some people choose to put off treatment depending upon the biopsy results.

Does anyone know of a Neurologist specializing in prolonged aura in the south east michigan or northern Ohio area? I have has this prolonged aura (currently in treatment) for over a year and a half and my neurologist just up and moved out of the blue and he was highly researched in the area.

I have been told in the past that my Vitamin D has been low. To be honest I did not feel that it effected me that much and mine was 13. However, doctors can vary on what they consider low. Right now it's 20 something and nothing feels any different.

I need mental health coverage, I seek therapy once a week for anxiety and depression and I need RX coverage, these meds are VERY expensive. I also need coverage for my skin, due to my acne meds. I a desperate, therapy and meds are too expensive out of my own pocket. Any info would help!

//fitnizz.

Is there any treatment for grave's eye disease to prevent the disfiguring look? Can you recommend a specialist in Michigan who is will knowledgable about the disease and willing to treat aggressively? Please help.

I was injured in a rear end collision. Because of the "no-fault" law in Michigan, it's unclear whether I have a case. I have had and continue to go to physical therapy. I work, but my strength in one arm is diminished and I don't sleep well. I don't have the energy and quality of life I had before the accident, and the doctor has diagnosed spondylosis, which may have been there but was triggered and accelerated by the impact.

You know, I wanted to mention and you probably know this already, that depression can be a PRIMARY symptom of MS. That is to say, there is depression that is expected from having a chronic illness for a long time. And there is primary depression of MS from actual damage done by lesions or demyelination. I hope you feel like your doctor is on top of this symptom for you, as it can be so very painful, but so very manageable.

look around online for a Michigan Lyme disease association -- some of these groups are better than others, but you might get lucky and get some leads to finding a good doc and friendly support for yourself (like here, only closer to home) 2rd: find a good Lyme doc 3rd: if the first doc doesn't click with you, find another one 4th: ALWAYS get copies of ALL your test results and keep them in a binder at home.

2 months ago I have been dignosed with policystic ovary syndrome. I was prescribed contraceptive pill as a treatment method but I am still experiencing a lot of discomfort and pain. I would like to know if there is another treatment method for this condition. I also feel that I haven't gone through detailed examination. Could it be another condition? What examinations do I need to undergo to be sure?

Michael Volk, MD, University of Michigan, Ann Arbor, Michigan, and colleagues obtained data of new patient prescriptions for pegylated interferon alfa-2a and -2b (Pegasys and Peg Intron, respectively) filled between 2002 to 2007. Results of the prescription audit showed there were 126,000 new prescriptions for pegylated interferon products in 2002 and by 2007 that figured declined to 83,000 prescriptions. Researchers project fewer than 1.

i am in alabama right now but am moving to michigan on wed. (family making me leave, really my step-dad who himself is and addict, alcoholic) (lived in michigan most of my life). my dad is there and he is a recovering alcohlic (been sober over 20 years!! go dad) so i know he will be very helpful. just feel a little defeated cause it was so hard to tell them, and i feel they are just getting the problem out of there hair.

Does anyone know a Doctor that specializes in POTS in Michigan they can recommend?

I have received injections from the University of Michigan Hospital in Ann Arbor, MI. Although they have greatly reduced my pain there is a limit to how many of these injections you can get due to muscular atrophy at the sight of injection. I am now at my limit and am wondering if there is any other treatment? Do you know anything about a neurostimulator? Several years ago I had tests that although they were slightly elevated, confirmed I do not have an autoimmune disease.

Are there clinics at low cost or no cost for the treatment of Hep C using interferon.

re not already on anti-depressants, they may be recommended before you start treatment as the treatment drugs can make depression worse.

ve been diagnosed with small intestinal bacteria overgrowth after 8 years of chronic diarrhea and multiple tests. I went to University of Michigan Hospital where the doctors performed a Hydrogen Breath Test. It was positive. I just finished the Cipro and probiotic. My question is this, since small intestinal bacteria overgrowth can be caused by taking acid blocking medicine like Nexium or Prilosec, will the bacteria come back since I continue to take Prilosec for GERD?

Hi,nice for me to hear that you haven't experinced depression,because I'm going to start my hep treatment tomorrow!! and I'm very very scary.I've been eroin user for years,years ago.I've been self medication with antideppressive for long time and all that let me some kind of swing mood,so I'm scare abaut the side effect of treatment.Never hear abaut people that developed skins prob ,way don't going to see a dermatologist?

Depression treatment michigan

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