Finding a Physician

This is one of the most difficult aspects of dealing with Chronic Fatigue Syndrome and Fibromyalgia.  Below are a few ideas.


 

 

   

Finding a Healthcare Provider

 

The National Fibromyalgia Association Doctor's List

The NFA has established a list of doctors across the U.S. who treat Fibromyalgia.  The NFA requires that you signup on their website to access the list, but signing up is free. 

 

Here is the link to their list.  http://www.fmaware.org/site/PageServer?pagename=resources_hcProviderDirectory

 

OFFER does not recommend or endorse any of these providers.  This list is for informational purposes only.  The information below is still very pertinent in selecting a healthcare provider.


There is much to consider when selecting a physician to treat CFS and FMS.  Here is an article from the CFIDS.org site, that may prove helpful.  http://www.cfids.org/about-cfids/choosing-a-doctor.asp


 
How to Talk to your Health Care Provider
Here are some additional thoughts:

IDEAS for Finding a Physician: by Lucinda Bateman, MD

 

1) Call your health plan and insist they help you find a physician who can provide good care for you, temporarily or permanently.  Put pressure on your health plan through the patient advocate department to have trained providers on the panel.  If they don’t have qualified providers, put pressure on the insurance plan to provide coverage out-of-plan for qualified providers.

 

2) Establish with a Primary Care Physician (PCP) who is accessible, capable and compassionate.  It doesn’t need to be someone with expertise in CFS or FM. A good PCP can assess symptoms, provide a diagnostic workup to exclude other underlying conditions, and help with symptomatic care.   Let your PCP know there is good information about CFS at the CDC website:  www.cdc.gov/cfs

3) You can often get in sooner and tend to pay less when you see a physician you have seen before, both generalists or specialists.  Physicians are more likely to gain experience with CFS/FM when they get to know you over time, rather than seeing you only once.  Teach your doctors about CFS/FM as you get to know them.  Your providers don’t need to be a specialist in CFS/FM to do a good assessment within their area of expertise (i.e. cardiology, gastroenterology, general surgery, etc). 

 

4) When you utilize an urgent care center (i.e. Instacare) for emergency medical issues, be sure to focus on the new, acute problem rather than your CFS/FM, which is a chronic illness.   Encourage the provider to focus on the urgent problem in a standard way (ie abdominal pain, chest pain, new infection, etc) and consider the CFS/FM only as a secondary underlying issue.   Be sure to provide good medical information, including old medical records stating your diagnoses, an accurate medication list, your bottles of medications, the names and contact information of your doctors, etc.

 

5) Patients with significant pain issues might try to get in to a Pain Clinic for help with opiate medications and other pain interventions. There are several in town.  Start calling around, and ask them who else might be open.  There is a growing awareness of FM among all physicians, but especially pain physicians.

 

6)  The most important thing to remember is that YOU should take responsibility for your own health.  Read and educate yourself.  Remind your physicians to keep your care up to date!  Know when you need lab tests (i.e. to monitor thyroid levels, or screen for medication toxicities) and when you should update your mammogram or PSA.  Be the proactive one to ensure it gets done.

 

 

CFIDS.org also has an excellent article on this subject

 

 Diagnosis and Treatment of FM A New Study for Fibromyalgia Patients Dr. Lucinda Bateman is actively seeking fibromyalgia patients, age 18-70, to participate in clinical research studies of three investigational drugs for the treatment of fibromyalgia. If you are interested, call Dr. Bateman's office (801 359-7400) and talk to Ali Allen, RN, research coordinator, or others on the research team, to learn more about the drug studies currently underway. Qualified participants receive study-related physician visits, lab evaluations and the investigational medication at no cost.  

Cause and Cure Pending: Treat the “Syndrome Subsets” of Chronic Fatigue Syndrome and Fibromyalgia Prescription Drug Assistance Programs   www.pparx.org Mayo Clinic's Health Symptom Checker  http://mayoclinic.com/health/DiseasesIndex/DiseasesIndex  Meditation for Fibromyalgia   

Would you like to participate in a research study on whether mindfulness meditation can help relieve Fibromyalgia symptoms? To qualify to participate, you need to be: Female and at least 18 years old.  Have a Fibromyalgia diagnosis from a physician.  Be relatively healthy, other than Fibromyalgia.  Be able to access the Internet from home.    For information about participating in the meditation study, immediately call (801) 585-7690.     "Does a single 25-minute period of moderate exercise have different effects on people with CFS and FM?"   Researchers are seeking FM and CFS patients to volunteer for a new study entitled, "Exercise Effects on Sensory Receptors and Cytokines in CFS and FM." The principal investigator is Kathleen Light, Ph.D., of the University of Utah Anesthesiology Department. The study is part of the University's new Program for Research on Mechanisms and Treatment of Chronic Fatigue and Fibromyalgia Syndromes, co-directed by Alan Light and C. Richard Chapman.    For information about participating in the exercise study, contact Dr. Lucinda Bateman at support@fcclinic.com or (801) 359-7400, or Dr. Andrea White at andrea.white@health.utah.edu or (801) 573-5387. ~~~  

National Data Bank for Rheumatic Diseases (NDB) Fibromyalgia Research is conducting research into factors that lead to the development of fibromyalgia. They need the help of people with fibromyalgia in researching this important issue.  For more information go to  http://www.arthritis-research.org/fibro.htm ww.arthritis-research.org/fibro.htm .