Fibromyalgia network newsletter

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fibromyalgia

875863 tn?1271603385 There are a variety of treatments for FMS. For example, the latest issue of the newsletter Fibromyalgia Network (www.fmnetnews.com) compares various drugs used to treat FMS. In our studies on FMS we found that over 70% of FMS patients had chronic infections (see our website www.immed.org for more information under Fatiguing Illnesses). If you have one or more chronic infections, these probably need to be treated. Also, for the fatigue we have found that NTFactor can help.
Avatar n tn Posted By Med Help International on June 04, 1997 at 14:38:51: In Reply to: Behcet's Disease and neuropathy posted by Judy Ford on May 27, 1997 at 18:10:12: Dear Judy: Med Help International suggests that you also contact the following organization, which helps patients who have been diagnosed with Behcet's Disease: American Behcet's Association National network. 18 affiliated groups. Founded 1978.
Avatar n tn Since its inception, the ICA has organized support networks throughout the US. In addition a newsletter is available that keeps patients abreast of the latest information regarding IC.The ICA would be the most appropriate network to obtain a reputable urologist in your area involved in IC treatment. The telephone number to the ICA is (212) 979-6057. The address is ICA/PO box 1553 MadisonSquare Station NY,NY/10159. This information is provided for general medical education purposes only.
627818 tn?1271777026 I don't know how many of you get the National MS Society newsletter online but yesterday's version had some interesting articles in it. There is some good research and clinical trials going on, so I thought that was encouraging! I'm sure you can go to the NMSS website - it is one those org ending sites, and sign up if you don't already receive it.
382218 tn?1341181487 The goal of endMS is to raise $60 million to fund research activities and establish the endMS Research and Training Network. In doing so, the MS Society aims to fund the best research, accelerate discovery in the field of MS and find a cure in the shortest possible timeframe. Accomplishments of the past year include: - the establishment of five regional research and training centres involving over 100 researchers and over 250 trainees - $41.
709222 tn?1229152836 I spent the day finishing the newsletter for Mason County Democrats. On the one hand I like doing this because I feel useful. On the other hand, there's a time deadline associated with it (which I often find stressful). Also I said when I took on this job that I didn't want to be involved in the mailing process, and it's been impossible to get out of the mailing process and still meet deadlines. It's not a big enough deal to quit over, but it is a stressor.
1178983 tn?1279663655 ) Otherwise, I know the National Fibromyalgia Association (www.fmaware.org/) lists local support groups by state on their website and you could probably Google some other resources too. I hope this helps.
773755 tn?1328119777 I was just reading a newsletter from another health site and it indicated some things that can affect fibromyalgia. MSG is definitely on the list as is aspartame.
Avatar f tn If you reside in the USA, have you heard about the Job Accommodation Network? This service is provided by the US Dept. of Labor (Office of Disab. Employment Policy). If you are an Employee - This site provides information on accommodation ideas, your rights under the American with Disabilities Act (keeping in mind that a disability does not mean it has to be permanent. One may become disabled only for a length of time, yet will still fall under the ADA).
999891 tn?1407276076 We are considering launching a “Chiari Newsletter on twitter or one of the other social networks” we propose to publish this on a weekly bases wth Chiari news, members experiences, latest on research being done ect …. We have been giving this idea some thought and would like your feedback and ideas ..... thank you.
Avatar n tn I AM LOOKING FOR SOME TYPE OF LEGIT NEWSLETTER THAT I COULD HAVE SENT TO MY AND MY FAMILIES E-MAILS...COULD YOU PLEASE DIRECT ME TO ONE? THANX!
Avatar f tn My obgyn recommended being tested for fibromyalgia and multiple sclerosis. The fibromyalgia test came back negative so i am trying to pursue testing for MS, however, my PCP of my HMO refuses to give me a referral to a neurologist and also refused my direct request for MRI. The PCP doesn't believe I have MS. My mental acuity continues to decline. Even had a couple instances of complete mental blockages.
463897 tn?1468013750 Who - or whom is actually writing the CL Newsletter? Are certain CLs being asked be write it - or portions of the Newsletter, as it sounds from some of the comments? Thanks for the responses I know I'll obtain.
Avatar n tn i have had mri and the dye/mri done as well i had already got fibromyalgia and my doctor has put me on lyric 600mg a day. but i am expercting numbness in my feet and hands more stiffness etc. but it seems like this lyrica d=has stopped helping me. is there another doctor i can go visit that is in my net work? could you please help me!!!!!!!!!!
Avatar n tn In addition to maintaining a network of resource centers, this organization sponsors education and training workshops, respite programs, support groups, and conferences. It also conducts consultations on the telephone and offers information and referrals. (FCA) http://www.caregiver.org Caregiver/Family The National Caregivers Association offers support and education for the 20 to 30 million people throughout the United States who provide care for a loved one.
Avatar f tn In addition to maintaining a network of resource centers, this organization sponsors education and training workshops, respite programs, support groups, and conferences. It also conducts consultations on the telephone and offers information and referrals. (FCA) http://www.caregiver.org Caregiver/Family The National Caregivers Association offers support and education for the 20 to 30 million people throughout the United States who provide care for a loved one.
Avatar f tn I also have lymphedema and I found a web sight that is very helpful. Its the National Lymphedema Network. There web sight is www.lymphnet.org. There E-mail address is ***@****. They have a newsletter that is very interesting. I was able to order a viedo from them that is a step by step, comprehensive maintence program for lymphedema patients. Good luck!
649848 tn?1534633700 On my profile page, I have checked the box to receive the MH newsletter, but I don't get it. I understand that there was a good video about thyroid in a recent newsletter and would like to find it. Can anyone tell me why I might not get the newsletter, even though I have that box checked? I know of, at least, one other person not getting it, as well. I'm getting other notifications, like I should.
Avatar f tn ) Tamra
999891 tn?1407276076 the newsletter will be on one page and archived with the publication of the new newsletter but we will have a link to the previous newsletter...we will have separate pages for things like related illnesses, Chiari Doctors and other such things...
1738291 tn?1316788003 Hello, I have a few questions which I thought some members could answer please 1) Is there a group/website/newsletter for a non-white/mixed race AS's and people who don’t have a problem with people of different colours and races in Norfolk or anywhere? Or a group/website/newsletter for non-white and mixed race etc which is aware and ok about AS's?
Avatar n tn check out the fibromyalgia network on the web. Sometimes fb presents during a mental health problem as well but only a knowlkedgable doctor concerning fb would understand! Good luck!