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Fibromyalgia

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  • Registered Users Posts: 34 Kenny Gofuk


    A very good friend of mine has of this June been told that she has this illness.
    It took her two years to get an appointment to see the specialist in Waterford.
    However after telling her that she has this he did not offer her as much as a disprin to ease her discomfort.
    He just recommended exercise.
    I am just curious as to what medication others of you were given and if it offered some relief?


  • Registered Users Posts: 1,937 ✭✭✭Tropheus


    There are several drugs used for Fibromyalgia. Aside from the usual pain meds, there is Lyrica and a couple of others that are similar. People have different experiences with Fibro so some react well to medications that do nothing for others. It's all trial and error.

    Exercise definitely does help if possible. However, not all people with FMS are able to tolerate exercise.


  • Registered Users Posts: 413 ✭✭thecelt


    Hope everyone is doing ok!
    This winter weather is def having an effect on the body!


  • Registered Users Posts: 1,275 ✭✭✭RubyGirl


    Is there anybody who has excessive sweating and put's it down to their meds. I'm on so much I would'nt know which one causes it, I can't wear make up at all and is so much worse in the summer of course. Is there anything I can do to help.


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    RubyGirl wrote: »
    Is there anybody who has excessive sweating and put's it down to their meds. I'm on so much I would'nt know which one causes it, I can't wear make up at all and is so much worse in the summer of course. Is there anything I can do to help.


    google side effects for your meds to try to find out. Als may help to find interactions between meds.

    I was once on 24 tabs a day, gradually dumped the lot and take very little now as side effects were as bad as the illness.


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  • Registered Users Posts: 413 ✭✭thecelt


    graces7, damn 24 a day!
    Was on a lot less but all it did was mess with my personality and moods and knock me out!

    Big change i have made was giving up dairy!
    Graces7 wrote: »
    google side effects for your meds to try to find out. Als may help to find interactions between meds.

    I was once on 24 tabs a day, gradually dumped the lot and take very little now as side effects were as bad as the illness.


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    thecelt wrote: »
    graces7, damn 24 a day!
    Was on a lot less but all it did was mess with my personality and moods and knock me out!

    Big change i have made was giving up dairy!

    For the chuckle thank you!

    And yes you are soooooo right. Mind you that was in the three decades they were saying I was mentally ill or just plain bad..

    When I managed to get the diagnosis of M.E I sorted myself out then left the country

    Now I tell the drs what I need as opposed to being under their control.

    ME and fibro and NOT mental illness so why do they insist on that kind of meds.

    And we have google and so many support groups.


  • Banned (with Prison Access) Posts: 38 cerise


    I have not had much success with physios for fibromyialga. I find pilates good and the heat and moving in the water. Have chronic pain from spinal disk disease lower and upper and referred pain from c5/6 . What therapies help or stauff that does not cost much money?


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    left hospital early y'day in sheer self defence,,,broke wrist and had to go for help finally..the fasting brought on a severe migrsine and we with m.e do not have the resources to deal with bright and noisy places.

    the ignorance of the young drs re both migraine and m.e appalled me so i demanded home

    trying even to get pain meds for the migtaine i was offered xanax and treated like a hypochondriac druggie

    at ovwe 70 i take a very dim view of that and am leary of the entire medical profession again
    thers no excuse.
    tried to change gp last year to no avail

    scuse bad typing!


  • Posts: 6,025 ✭✭✭ [Deleted User]


    cerise wrote: »
    I have not had much success with physios for fibromyialga. I find pilates good and the heat and moving in the water. Have chronic pain from spinal disk disease lower and upper and referred pain from c5/6 . What therapies help or stauff that does not cost much money?

    Water therapy is very good for us who have fibro :) Certain pools around Dublin offer it, not sure where you are, but you could google it.

    The warm water really helps the muscles.

    I did it last year at the Hospice in Harolds Cross as part of the pain management program. found it be to very helpful.


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  • Banned (with Prison Access) Posts: 38 cerise


    Thanks for that info Jake. I have noticed am good in warm water and when pools are lowering their temp a bit it makes a negative difference. whose Pain management programme are you on and how do you get on it if you don't mind me asking? :)


  • Posts: 6,025 ✭✭✭ [Deleted User]


    cerise wrote: »
    Thanks for that info Jake. I have noticed am good in warm water and when pools are lowering their temp a bit it makes a negative difference. whose Pain management programme are you on and how do you get on it if you don't mind me asking? :)

    No problem :0

    I was refered to the 'Program' , not exactly sure what its called, but its along those lines :)

    I was refererred by Consultant, Prof Cunnane in St James Hospital, Dublin.
    I was a day patient, 4 times a week at first, you basically attend every morning, get in pool, do a circuit of exercises. At first you are really exhausted and dehyrated, by you get used to it. The heat is brilliant, after the first week, I was already starting to feel the benefits. After the pool therapy, you might do occupational therapy, they go through things that just make day to day life a little bit easier.
    Then , you do meditation for about half an hour. This too is very useful, for me it was anyway.

    Then it would be lunch time, so its off to canteen.

    After noon it would be exercise and heat massage.


    It was one of the best things I ever did since I was diagnosed with Fibro. The staff are wonderful, I really mean it, couldnt say enough good things about the place.

    I used to think of the Hospice, as a place of end of life treatment. They have helped me get some quality of life back.
    Very grateful to them all.
    So I would highly recommend asking your Consultant about it.

    Best of Luck :)


  • Registered Users Posts: 86 ✭✭roxana


    I know it's an old topic, but I have to try. How are you? Have you found treatment that is actually working?
    I'm working part time, but feeling worse and/or (even) worse, my GP suggested to go on Illness Benefit, but when I checked info... I'm still shocked :[ 120e per week? whaaa? How do you manage to live for 120euro per week? jesus, maybe I should start to dig my own grave instead :(


  • Registered Users Posts: 2,115 ✭✭✭misstearheus


    I'm going through an awful bad patch this week. ;(:( It has never been this bad. Am absolutely flummoxed with fatigue for the last few days. I'm really getting scared now, I've slept for the last 4/5 days pretty-much solid, have managed to get up a couple of hours in the middle of the day to do a couple of things around the house but it's horrendous. I really havn't eaten in the last few days or nothing. :( I'm far too tired to function or do anything at all at the minute, cooking, putting down a fire. It's just too risky. I don't know if this is just a really bad flare-up this week, or if it's a sign of things to come. But I'm getting worried now, if this is what it's gonna be like, I won't be able to live independently, I'm gonna have to move back home. ;( It's awful. :/

    My skin is a mix of purple and green and ashen-colour all day lol but I think it's back to itself now. My glands are sore. I'm starting to get headachey now and have pain in my nose like I've been eating ice-cream lol. I've un-luckily somehow managed to get my period even though it's not due for another while yet and that's a killer coz it's doubling the fatigue on me at the mo. I've some sort of a chest-infection too at the moment and I'm wrecked and exhausted from all the coughing. Every last muscle in my body is starting to get sore. I went to the shops and Chemist today to stock up on supplies so hopefully all that stuff will knock me out now soon! It's really hard isn't it!


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    roxana wrote: »
    I know it's an old topic, but I have to try. How are you? Have you found treatment that is actually working?
    I'm working part time, but feeling worse and/or (even) worse, my GP suggested to go on Illness Benefit, but when I checked info... I'm still shocked :[ 120e per week? whaaa? How do you manage to live for 120euro per week? jesus, maybe I should start to dig my own grave instead :(

    Well, we manage.. There are some additional benefits also. look at the excellent Citizens information web site. eg Household Benefit package, rent allowance, solid fuel allowance. Do check before you pick up a spade! Citizens info are excellent.


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    Jake1 wrote: »
    No problem :0

    I was refered to the 'Program' , not exactly sure what its called, but its along those lines :)

    I was refererred by Consultant, Prof Cunnane in St James Hospital, Dublin.
    I was a day patient, 4 times a week at first, you basically attend every morning, get in pool, do a circuit of exercises. At first you are really exhausted and dehyrated, by you get used to it. The heat is brilliant, after the first week, I was already starting to feel the benefits. After the pool therapy, you might do occupational therapy, they go through things that just make day to day life a little bit easier.
    Then , you do meditation for about half an hour. This too is very useful, for me it was anyway.

    Then it would be lunch time, so its off to canteen.

    After noon it would be exercise and heat massage.


    It was one of the best things I ever did since I was diagnosed with Fibro. The staff are wonderful, I really mean it, couldnt say enough good things about the place.

    I used to think of the Hospice, as a place of end of life treatment. They have helped me get some quality of life back.
    Very grateful to them all.
    So I would highly recommend asking your Consultant about it.

    Best of Luck :)

    This highlights the difference between fibro and M.E. No way could that be done with M.E.. glad you are benefitting!


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    I'm going through an awful bad patch this week. ;(:( It has never been this bad. Am absolutely flummoxed with fatigue for the last few days. I'm really getting scared now, I've slept for the last 4/5 days pretty-much solid, have managed to get up a couple of hours in the middle of the day to do a couple of things around the house but it's horrendous. I really havn't eaten in the last few days or nothing. :( I'm far too tired to function or do anything at all at the minute, cooking, putting down a fire. It's just too risky. I don't know if this is just a really bad flare-up this week, or if it's a sign of things to come. But I'm getting worried now, if this is what it's gonna be like, I won't be able to live independently, I'm gonna have to move back home. ;( It's awful. :/

    My skin is a mix of purple and green and ashen-colour all day lol but I think it's back to itself now. My glands are sore. I'm starting to get headachey now and have pain in my nose like I've been eating ice-cream lol. I've un-luckily somehow managed to get my period even though it's not due for another while yet and that's a killer coz it's doubling the fatigue on me at the mo. I've some sort of a chest-infection too at the moment and I'm wrecked and exhausted from all the coughing. Every last muscle in my body is starting to get sore. I went to the shops and Chemist today to stock up on supplies so hopefully all that stuff will knock me out now soon! It's really hard isn't it!

    You MUST eat even if Complan or similar. You really must fuel your body. We have all been through the not eating thing and learned the hard way that this makes it worse. While you are out, stock up on easy foods. You will just get weaker and worse if you give your body nothing t work with especially if you are in bed most of the day. Need to get up and walk round every hour and get water , or milk or bread and jam even!! It is very hard but you can do it. When I was at my worst I used to get out if bed every hour, bathroom, flll my water jug, check on the critters I had then, eat something however small, then back to bed. I still get days like that ; grit your teeth time! Food matters and your mood will go down and down if you fail to eat. Up to you! Blessings and peace and I am offline soon for the day...


  • Registered Users Posts: 1,634 ✭✭✭Gehad_JoyRider


    Hi I'm new I know the thread is old but I'm going through the whole process past 8 weeks now. I can't work for the pain. I spend most my days making trips to the kettle to refill my hot water bottle I've never felt pain like this before.

    It's pretty debilitating, trying to keep a positive outlook but I won't lie seems pretty hard.

    Anyone got any advice?


  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    Hi I'm new I know the thread is old but I'm going through the whole process past 8 weeks now. I can't work for the pain. I spend most my days making trips to the kettle to refill my hot water bottle I've never felt pain like this before.

    It's pretty debilitating, trying to keep a positive outlook but I won't lie seems pretty hard.

    Anyone got any advice?

    What pain relief works for you?


  • Registered Users Posts: 1,634 ✭✭✭Gehad_JoyRider


    Graces7 wrote: »
    What pain relief works for you?


    CBD oil helps coupled with some of my pain meds and a hot water bottle it really depends on the level of pain, Im experiencing.

    If I was to put on a sacale of how rough I'm feeling today, I'd say a safe 8 :(.


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  • Registered Users Posts: 32,634 ✭✭✭✭Graces7


    CBD oil helps coupled with some of my pain meds and a hot water bottle it really depends on the level of pain, Im experiencing.

    If I was to put on a sacale of how rough I'm feeling today, I'd say a safe 8 :(.

    Think you need to get your pain meds reviewed?


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