Many individuals believe that the condition known as Fibromyalgia is a hereditary condition and can be passed down from generation to generation. However studies have shown that although this is the case in some families it is not the case in others – here we look at the case for and against.
Is Fibromyalgia Hereditary?
Studies have shown in recent years – and most of these studies it should be pointed out were carried out in the United States as the medical community in the United Kingdom are still unsure as to the causes of Fibromyalgia – that there is roughly a twenty five per cent chance you will suffer from Fibromyalgia if one or other of your parents have suffered from it.
Information would indicate that women are more likely to contract the illness than men and that it can lie dormant in an individual’s body until a traumatic event triggers it off. Such traumatic events would include:
- Child birth
- Pneumonia
- Being involved in an accident
- Problems with the Thyroid
Many mothers and daughters share the same symptoms of Fibromyalgia and indeed many daughters fall foul of the condition shortly after they have given birth to their first child. It would appear that there is a genetic link between mothers and daughters but the link between fathers who have the condition and their sons is not as easily identified. This may be because that although men can suffer from the condition there are not as many men suffering from it as there are women.

Describe your current flare up and we will help you identify likely triggers and what might ease it.
Try our Flare Up Analyser free, here on this site →How Do I Know if I am Suffering from Fibromyalgia?
This is a difficult question and one that many doctors find difficult to answer; because Fibromyalgia and M.E (Myalgic Encephalomyelitis) both have similar symptoms doctors can sometimes misdiagnose the condition. Likewise because both Fibromyalgia and M.E (Myalgic Encephalomyelitis) exhibit overlapping conditions such as Insomnia, Irritable Bowel Syndrome (IBS) and Chronic Fatigue they are often difficult to diagnose at all.
Many patients suffering from either Fibromyalgia or M.E (Myalgic Encephalomyelitis) find that it can take anything up to two years before they receive a final diagnosis as to what the nature of their condition actually is.
There are symptoms associated with both conditions that should set alarm bells ringing and thus have you making an appointment to see your doctor. These include:
- Insomnia
- Fatigue
- Heavy limbs
- Headaches
- Nausea
- Pins and needles
- Short-term Memory problems
if you suffer from any of the aforementioned conditions with any regularity you should make an appointment as soon as possible to see your doctor. Also it is worth while keeping a diary of your experiences so that he or she may make a more informed diagnosis.
Your situation may be slightly different. ask a question below ↓ and our editorial team will reply with our advice.
What Should I Do if I am Diagnosed with Fibromyalgia?
If you have been diagnosed with either Fibromyalgia or M.E (Myalgic Encephalomyelitis) then the first thing is not to panic. This may sound easier said than done but you should try and remain calm and positive. Many individuals suffer from both Fibromyalgia and M.E (Myalgic Encephalomyelitis) and manage to live productive and active lives. However it should be said that if you have contracted the more chronic version then you may find activities that you took for granted more difficult and much more tiring.
Many people panic when they find out that neither Fibromyalgia or M.E (Myalgic Encephalomyelitis) have a cure; the most you can hope for is to keep the condition under control by taking regular breaks to rest, changing your diet and your lifestyle, and trying to remain positive throughout.
He has good days and bad days but when he tries to do little jobs his muscles go into spasm.
I know he will not be able to manage the garden and we will have to employ a gardener.
He retired 4 years ago I was wondering if he could claim any kind of living allowance we have never claimed for anything before so we are new to this.if anybody can give me advice I would be very grateful .
I was diagnosed with athritis ... (((( which doc said ))))) but its was different as I new what
Atheist is was as my mother had it .... in 2005 ... then one day at work I collapsed with
Uncontrollable pain all over my body .....I had a dexa scan and it resu
Ted that I have fybromyalgia and borderline osteoporosis .... so in 2009 my docter signed me off work ...and since then I've been in such cornice pain ..
At first it took me 4years of so much stress to claim for dla ....the hell I was pit threw
Which made my illness worse ... I felt so worthless as I've always worked all my life .
I have many allergies . And avoid certain foods ... I recently claimed for pip .
And I have a walking stick I have all the symptom depression stiffness Fatique brain fog weight gain ,that due to la k of movement and amitripaline ,and because I signed but name they sd I was ok .and took it away from me ..... it's disgusting ....how people get treated .they cause us more stress ......but it's ok I recently married and my husband is so kind and helps me ..
Thankyou for listening and reading my comment .... it's so lonly at times ...
I also have not had great experience with doctors.. But that also comes with the mental health stigma. Pretty much as soon as you say "I have PTSD" or anything like that they decide oh.. Must be a mental thing. And tend to blow you off. Besides telling me I need to be on Psych meds.. Which have only ever worsened my mental conditions. I have been med free over 3yrs and haven't needed the ER every month like I used to. Anyway.. I was looking to see if this fibro was hereditary.
I was told my aunt and her daughter drink something called Jamaica. That and taking milk out of their diets I was told reduced their pain by 80%. Not sure about the other symptoms though. I am still concerned about the other symptoms Such as stiff joints, memory problems, dry eye bouts, vision changes, dizziness and balance, etc. Seems like everyone just thinks it's JUST pain when it is SO MUCH MORE.
Also I'm so cross that my whole life has been ruined by fybro.
My mother has severe arthritis, my eldest sister has arthritis, but there symptoms are literally the same as mine, but i dont think they want to be diagnosed.
I believe its because our mitrochondia is damaged and we are passing it down.
Be great to be able to break the link my my girls in time will have healthy children themselves.
Ask Fibromyalgia Syndrome a question
Ask our editorial team a question and we will reply with our advice. Tell us as much about your situation as you can: the more detail you give, the more useful our answer can be.
You do not need to use your real name. Please do not include your full address, phone number, email address, or the names of other people. We may edit or remove identifying details for privacy and legal reasons.
Comments are moderated before publication.