Polls - Andover Fibromyalgia & ME Community Group | HealthUnlocked

Andover Fibromyalgia & ME Community Group

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How would you measure your pain level out of 10 during a bad flare?

Which of the following do you feel personally helps you to live with the symptoms of Fibromyalgia and/or ME?

Regarding your diet, which of the following do you avoid hoping to reduce the severity of your symptoms?

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In your opinion, what were the main factors that hindered your diagnosis of Fibromyalgia & ME which made it a lengthy process?

Vitamin deficiency seems to be common in both Fibromyalgia & ME, so have you been found to be deficient in any of the following?

Did you have Epstein Barr Virus (ie Glandular Fever) or an immunisation that you feel may be a cause of your diagnosis?

Have you ever experienced any stigma surrounding Fibromyalgia and/or ME by a Health Professional?

Do you know whether you were ever tested for Lymes disease before a diagnosis of Fibromyalgia and/or ME?

Do you have primary Fibromyalgia or Secondary (due to an existing illness)?

What are your experiences of Graded Exercise Therapy (GET) ? Did it help your condition, after your pain was controlled & symptoms reduced?

What multi chemical sensitivities do you have with either Fibro or ME/SEID?

In your opinion, how is the best way to raise awareness daily?

In your opinion do any of you think you have had a diagnosis of Fibromyalgia but think you may have ME as well & vice versa?

Do you ever get swollen glands with your Fibromyalgia or ME?

Which of the following therapies have you tried to help alleviate your symptoms of Fibromyalgia and/or ME alongside your medical treatment?

In your opinion, how many times do you feel your diagnosis has been dismissed by a Healthcare Professional ?

Which UK Charity website do you use to find information on Fibromyalgia or M.E ?

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