Polls - Andover Fibromyalgia & ME Community Group | HealthUnlocked

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Polls - Andover Fibromyalgia & ME Community Group | HealthUnlocked

Andover Fibromyalgia & ME Community Group

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?

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

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