Results of the King' s college study? - Fibromyalgia Acti...

Fibromyalgia Action UK

59,987 members67,154 posts

Results of the King' s college study?

phlebo123 profile image
13 Replies

Almost 12 months ago I (and I believe other members of this community) donated blood samples for a DNA study on fibromyalgia and chronic pain. Does anyone know if any results or conclusions have been found from this study? The letter I received with the blood test kit suggested that this research may improve diagnosis and treatment in the future. Does anyone know how I would find out if they have any results that may be useful to us?

Written by
phlebo123 profile image
phlebo123
To view profiles and participate in discussions please or .
Read more about...
13 Replies
Mazz64 profile image
Mazz64

Hi, I was not on here then, but perhaps if you phone Kings college hospital they may be able to help, I would like to know the out come of that.

sorry I'm not more help

Speedqueen9 profile image
Speedqueen9

My brother and I took part in it as well . I suspect it is going to be quite a long in depth study but like you we are hoping that we will hear something about there findings. I was just happy that someone seemed to be doing something to help us at last instead of just telling us it's all in our heads :(. Fingers crossed that they come up with something soon xx

Mel68 profile image
Mel68

Iwd like to know results and wd have participated if I had knowm in the Uk

sue32 profile image
sue32

I was wondering the same thing! I do hope we get the results at some point! XX

It's possible, and indeed likely, that they won't make the results public until they have published them in a medical journal. I'm an academic and I know this can take many months and sometimes up to 2 years. By all means phone the University if you have details of the department and ideally the researcher undertaking the study and ask. They may be willing to tell you something over the phone. It would be wonderful if it helps!

Mdaisy profile image
Mdaisy in reply to

Very true - This is the usual course of things. Thank You for commenting

Saskia profile image
Saskia

I registered with them but was never sent a kit and, at the time, I just didn't have the energy to pursue it. I would gladly have taken part. I, too, would be very interested to learn of any findings. It would be great if the research found some genetic links which might give a clue as to why some of us are prone to this illness. Even better if they could come up with some beneficial treatment or even a cure. Wishing everyone as pain free a day as possible. Hugs XX Saskia.

Glenys profile image
Glenys in reply toSaskia

Same here, I didn't get a kit, or any email back?

LaurieLee profile image
LaurieLee

I completed the study with blood samples only few months ago, even thou the nurse could only get 1.5 vials of blood instead of 3. Even thou I applied over a year ago initially. So probably a few years to go for results, as they are still in early stages. X

dave2882 profile image
dave2882

this study is still on right now its taking a long time so far they have tested around 950 people and are hoping to get 2000 people to do the testing still not had mine samples all the best dave

Glenys profile image
Glenys in reply todave2882

Well, I imagine they may be quite busy still, so I might try again, then. Although getting my doctor to comply might be a problem though.......

Glosgran profile image
Glosgran

fmauk.org/articles/41-medic...

phlebo123 profile image
phlebo123 in reply toGlosgran

Thanks for posting this link... so pleased to hear that the research is making good progress... let's hope that the research shows something positive!!

Not what you're looking for?

You may also like...

FIBROMYALGIA STUDY KINGS COLLEGE LONDON (BLOOD SAMPLE)

Hi I wanted to participate in this study but my GP's surgery wants to make a £15.00 charge for...
jiw8207 profile image

I had my blood drawn for the FM/a fibro test.

I had my FM/a blood test done Tuesday and it was shipped overnight to Los Angeles. I should know...
WorldOHurt profile image

Is anyone involved in the FMA Genetic study

I came across the Fibromyalgia Association UK website and they are carrying out a UK wide genetic...
shazzap12 profile image

Bruising

I visited my GP 2 weeks ago re unexplained bruising on various parts of my body, she took a blood...

PEOPLE NEEDED FOR THIS STUDY, FULL INFORMATION IS INCLUDED IN THIS POST. sorry my last post missed the webaddress to apply.

CALLING PEOPLE WITH FIBROMYALGIA WE NEED YOUR HELP TO COMPLETE THE LARGEST GENETIC STUDY OF...

Moderation team

See all
Hazel_Angelstar profile image
Hazel_AngelstarAdministrator
Lynda_FMA_UK profile image
Lynda_FMA_UKModerator
Sarah_fmauk profile image
Sarah_fmaukModerator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.