• MyFibroTeam

MyFibroTeam

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MyFibroTeam has a rating of 2.5 stars from 2 reviews, indicating that most customers are generally dissatisfied with their purchases. MyFibroTeam ranks 444th among Social Network sites.

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Reviews (2)

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Thumbnail of user mewm2
1 review
3 helpful votes
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January 21st, 2019

While I appreciate what they are trying to do with this website, after spending over a year of infrequent use on Myfibroteam I've deleted my membership.
The site attempts to connect fibromyalgia suffers across countries, it can be used to make friends, build support teams and discover/utilize existing resources (like local, in person fibro support groups or treatment centers). Perhaps the biggest drawback of the site is that it functions a lot like Facebook. Members are encouraged to share their status updates, random strangers will add you to their support team when they have zero intention of communicating with you and they're not even from your country (these are MFT's version friend collectors, they just like piling on the friends list to make themselves feel important). A lot of users join only to drop off of the site completely shortly thereafter, either because there are no resources where they live or for the most exhausting reason: the fact that everyone comes to the site to vent.
A lot of members come on to complain about their pain or how it's effecting their lives. While I can understand that they feel distressed and come to MFT for support, it can be utterly overwhelming or just downright annoying. As a fibro sufferer the one thing I've learned is that eventually you need to stop talking (or rather complaining) about the pain. A lot of members come on just to gripe about the pain and explain things that need not be mentioned; what difference does it really make if your shoulders hurt today when you already mentioned it yesterday, and the day before that? It's like being stuck in a negative thought cycle, people should be encouraged to think positive and not give us a detailed day to day account of their symptoms. Even when you try to help these people it goes nowhere, they'll make excuses or just complain some more. It's so common and and so bad that one of the "reasons for deleting account" options is "overwhelming", like the people who operate the site are well aware of this problem!
It's also distressing when people come on feeling suicidal or unstable, while this talk is generally discouraged it still comes up and for some people that might be incredibly difficult to take. Another thing that is discouraged is suggesting medications/treatments, as everyone is different and nobody is a certified medical practitioner, it's not ok to tell someone take "x" drug for your pain, but when I was on people were still doing it.
I wrote MFT a detailed account of my concerns outlining many of the aforementioned problems, but I never heard back from them. I think in the future it really ought to behave solely as a resource website that casually allows networking with less of an emphasis on membership and more on information.

Thumbnail of user marym69
6 reviews
16 helpful votes
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August 28th, 2021

It's not a blog you can actually put in all your information, they want you to only "comment" on their professionals, which at times gives disputed information ("Fibro is a result of Depression/Anxiety and therefore you need to take antidepressants to deal with your Fibro". Fibromyalgia is a syndrome that has no known cause based on shared symptoms not on causality, and while someone can have depression or anxiety as a RESULT of having Fibro, it is not the cause of the condition unless the person was diagnosed with anxiety or depression BEFORE having the diagnoses finding Fibromyalgia). I am a bit frustrated with the 'professionals' that are posting. Many of the comments are highly Christian which is FINE if this is agreed that the site is geared for only Christian support. For those who are not, will find themselves isolated there further than before joining this website, because being told to "quit complaining and consult your Bible" (as one member suggested to someone feeling at the end of their rope), was pretty demeaning and insensitive. This should have been a way to report this to a moderator but there is no where to suggest that posts need reviewing. Another post suggested "Eureka! They found the cure for Fibro" which again, was based on a sales ad that the member couldn't understand was just an ad and would give 'false hope'. Lastly, getting 20 emails a day or more sending "hugs and likes" isn't the same as connecting with others. At first this seem nice, but you spend a great deal of time consoling others, great deal of time explaining Fibro to folks and a great deal of time correcting misinformation. I joined the site for new information on Fibro, connecting with others that have this condition, only to find that YOU do all the work, their professionals at times give seriously faulty information (that can't be turned in as incorrect) and is a wonderful hot bed of support only if you are Christian. If you want a support group that doesn't take every day work, clog up your email, and requires you to increase the people you connect up with, i would find a page elsewhere that actually does support, and offers you allies that can assist you living with an illness, not make you work harder.

Tip for consumers:
Realize they will constantly want you to ADD new contacts to your account on MyFibroTeam or any of the other medical accounts they have created. You will be faced with misinformation at times and also heavy Christian overtones as well as "Amens" etc. If you are not Christian, you might find a better place to connect with those with your condition, rather than a site that allows all faiths, as well as all genders. It is important to know that most of the work will be done by YOU, not by others

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