General fitness, health and nutrition · Public discussion

Check-ups/Pacemaker etc

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General fitness, health and nutrition
Published
1 October 2003
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3 October 2003
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  1. Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana

  2. <[email hidden]> wrote in message
    news:[email hidden]...

    Quoted message said:

    Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana


    A friend who had a pacemaker fitted last November (NHS, no sedation:-)) was
    told on his first check up that if he has any problems or worries just to
    phone the clinic and they will see him. He has had the device adjusted
    several times and now goes hill walking again.
    Derek.

  3. Quoted message said:

    Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    You should inform your doctor about the increasing joint pain.

    Quoted message said:


    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana

    Sounds like you should call for a sooner appointment since the increasing
    joint pain and the constipation are active issues.

    --
    Dr. Andrew B. Chung, MD/PhD
    Board-Certified Cardiologist
    http://www.heartmdphd.com/

  4. As far as verapamil and the pacer, it depends on what kind of pacer you
    have. It sounds like a run of the mill variety which first stimulates your
    SA node (causes the atria to contract) and then the AV (the ventricular
    counterpart). What these pacers generally do is prevent your heart rate
    from dropping below a certain point which is set by the doc. For instance,
    if your pacer is set at 72 beats a minute and your own heart rate falls to
    65, the pacer will recognize this and kick in to bring your heart rate back
    up to 72.

    What pacers do not do that verapimil does is prevent your heart rate from
    going to high. Even when pacers have a ramping feature which overrides the
    intrinsic rhythm or a defibrillator implanted with them, it is often
    unpleasant, although life saving, when they kick in. Therefore, it could be
    that your doc wants to protect you from both a low heart rate and a high
    heart rate. Neither are very good.

    You say that you really need your pain meds now. Why is that? There is
    nothing intrinsically painful about a rhythm problem.

    I have not heard of verapamil causing joint pain but most of my experience
    is in CCU. If you have long term chronic joint pain, regardless of the
    cause, it should be addressed by an ortho doc or a rheumotologist (if it is
    related to arthritis).

    Without reading too much into your post, I guess I am disturbed by all the
    attention to your pacer and the heart drugs, while you clearly state you
    'need' your pain meds. It is not unusual for patients with legitimate pain
    to develop a dependency on pain meds. Please forgive if I read too much
    into your post. There are chronic pain clinics that can offer you relief of
    joint pain. I have seen wonders worked with physical therapy. How much do
    you weigh? I lost twenty something pounds a few years ago because of my
    knees. Nothing else would motivate me. I still need to lose 20 or so
    pounds but damn if the joint pain isn't resolved!

    You need to be able to trust your doc. I know many cardiologists and heart
    surgeons. When I am called for advice, I always take into consideration the
    personality of the patient. I know a couple of docs that I don't
    particularly care for but if I code, I want them there. There are docs who
    really respect the patient's right to make an informed decision and go to
    great lengths to carefully lay out all their options and they don't fit well
    with patients who really don't want to know! So, without saying that your
    doc is bad, you may want to shop for another.

    Constipation is a minor problem unless you are the one suffering🙂 There
    are other remedies other than stopping meds. The best one I can think of
    eating well and exercising. The addition of fruits and veggies to your diet
    and walking would be good for anyone. If you change the amount of green
    leafy veggies you eat, you should call your doc and have your PT/INR
    checked. It is erroneous info that coumadin patients shouldn't eat green
    leafy veggies. Rather, the dosage should be adjusted to the patient's diet.
    For you, that means eating whatever quantity you desire on a regular basis
    and informing the doc if that changes. Yogurt keeps your gut healthy and
    there are some pharmaceutical remedies that help. Again, I worry that if
    you are taking pain medication with a sedative effect on a regular basis,
    your drive to exercise might be diminished.

    I wish you well. Please check back in. I apologize if I read too much into
    your post concerning your need for pain meds. It has never been and will
    never be my desire to have a patient hurting. Rather, for long term chronic
    pain, there are other answers besides pain meds.

    j

    <[email hidden]> wrote in message
    news:[email hidden]...

    Quoted message said:

    Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana

  5. I'd like to try to help. When you speak about your valve you are talking about
    the plumbing of your heart. When you talk about your pacer you are talking
    about the electrical system. True, your valve problems may have something to
    do with your supraventricular rhythms, however the pacemaker only responds to
    the brady rates, that is unless you have something like a Medtronic AT 500 that
    will treat high atrial rates.The verapamil deals with these high atrial rates
    and the digoxin makes your heart more effective as a muscle. The pacemaker
    both protects you from having a slow heart rate which can come as a result of
    your medications and/or sick sinus syndrome. The pacemaker stimulates your
    heart to beat, the digoxin makes each contraction stronger and the verapamil
    keeps the upper chambers of the heart from having high rates as in atrial
    fibrillation, atrial flutter and SVT.

    As for regular visits. Pacemakers should be checked every six months in the
    clinic. A full interogation should be done at that time. Your pacemaker
    outputs should be optimized at that time to extend battery like. While most of
    the insurance HMO's will not pay for more frequent checks, if you should have a
    problem,have any cardiac symptoms, always call your cardiologist and have him
    see you. As your pacemaker gets older and the battery voltage declines the
    checks will become more frequent so that the battery status can be monitored.

    As your cardiologist questions when you have one. Do not be afraid. There
    is nothing wrong with wanting to know what is happening and being done to your
    body. Patients go to MD's with all levels of medical knowledge and sometimes
    the DR overestimates the patients understanding, so speak up if you have a
    question.
    As for the joint pain....I am not a physician. I would check with your
    primary care MD and let him look for the cause. He would be the right person
    to see for your issue.

    If I can add anything else feel free to ask.

  6. I will try to give you and 'Complex' more info,as, in my first
    message, I was trying to be brief in case I repeat the stuff people
    have heard before. The last diagnosis I was given was paroxysmal AF
    and flutter and 2:1 AV block. The pacer is set to prevent my heart
    beat going below 60 or above 130. I need my pain meds for widespread
    osteoarthritis; neck, shoulders, spine, hands etc and the danger of
    dependency is something I am aware of. I take 4 painkillers each day,
    one co-codamol and one tramadol when I wake up and 2 co-codamol in the
    afternoon. I had three major procedures in a 15 month period ending
    last November. The first procedure was to remove a Duke's A tumour
    from my colon (outlook very good). It is now two years since that one
    and there have been no worrying symptoms. But, because my colon has
    had a large section section removed I tend to worry about using
    laxatives but I do use them as I am too uncomfortable otherwise.

    About two months ago I saw a rheumatologist and will be having a
    steroid injection in my shoulder - but, the appnt is not until Dec.
    This is the down side of our free National Health Service. My GP has
    given me amitriptyline (25mg) but it seems to interact with the
    verapamil i.e. I feel zombie like the following day so I stopped
    taking it.

    I do have good cardiologists. The 'chief' is a Professor who is said
    to be an authority on pacing. Unfortunately, there has been a big
    upset in our relationship. All his registrars are great but he seems
    to have a very high opinion of himself and I . As a result I am
    reluctant to ask for earlier appointments or leave messages with his
    secretary. (I suspect the Prof. resents the fact that my surgery was
    done at a different hospital..even though the new procedure I had for
    AF did not go well for me)
    It is possible I will be seen by a different consultant in future.

    Thank you both for your responses.
    Diana

    On Wed, 1 Oct 2003 21:01:07 -0500, "Julianne" <[email hidden]>

    Quoted message said:

    As far as verapamil and the pacer, it depends on what kind of pacer you
    have. It sounds like a run of the mill variety which first stimulates your
    SA node (causes the atria to contract) and then the AV (the ventricular
    counterpart). What these pacers generally do is prevent your heart rate
    from dropping below a certain point which is set by the doc. For instance,
    if your pacer is set at 72 beats a minute and your own heart rate falls to
    65, the pacer will recognize this and kick in to bring your heart rate back
    up to 72.

    What pacers do not do that verapimil does is prevent your heart rate from
    going to high. Even when pacers have a ramping feature which overrides the
    intrinsic rhythm or a defibrillator implanted with them, it is often
    unpleasant, although life saving, when they kick in. Therefore, it could be
    that your doc wants to protect you from both a low heart rate and a high
    heart rate. Neither are very good.

    You say that you really need your pain meds now. Why is that? There is
    nothing intrinsically painful about a rhythm problem.

    I have not heard of verapamil causing joint pain but most of my experience
    is in CCU. If you have long term chronic joint pain, regardless of the
    cause, it should be addressed by an ortho doc or a rheumotologist (if it is
    related to arthritis).

    Without reading too much into your post, I guess I am disturbed by all the
    attention to your pacer and the heart drugs, while you clearly state you
    'need' your pain meds. It is not unusual for patients with legitimate pain
    to develop a dependency on pain meds. Please forgive if I read too much
    into your post. There are chronic pain clinics that can offer you relief of
    joint pain. I have seen wonders worked with physical therapy. How much do
    you weigh? I lost twenty something pounds a few years ago because of my
    knees. Nothing else would motivate me. I still need to lose 20 or so
    pounds but damn if the joint pain isn't resolved!

    You need to be able to trust your doc. I know many cardiologists and heart
    surgeons. When I am called for advice, I always take into consideration the
    personality of the patient. I know a couple of docs that I don't
    particularly care for but if I code, I want them there. There are docs who
    really respect the patient's right to make an informed decision and go to
    great lengths to carefully lay out all their options and they don't fit well
    with patients who really don't want to know! So, without saying that your
    doc is bad, you may want to shop for another.

    Constipation is a minor problem unless you are the one suffering🙂 There
    are other remedies other than stopping meds. The best one I can think of
    eating well and exercising. The addition of fruits and veggies to your diet
    and walking would be good for anyone. If you change the amount of green
    leafy veggies you eat, you should call your doc and have your PT/INR
    checked. It is erroneous info that coumadin patients shouldn't eat green
    leafy veggies. Rather, the dosage should be adjusted to the patient's diet.
    For you, that means eating whatever quantity you desire on a regular basis
    and informing the doc if that changes. Yogurt keeps your gut healthy and
    there are some pharmaceutical remedies that help. Again, I worry that if
    you are taking pain medication with a sedative effect on a regular basis,
    your drive to exercise might be diminished.

    I wish you well. Please check back in. I apologize if I read too much into
    your post concerning your need for pain meds. It has never been and will
    never be my desire to have a patient hurting. Rather, for long term chronic
    pain, there are other answers besides pain meds.

    j

    <[email hidden]> wrote in message
    news:[email hidden]...

    Quoted message said:

    Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana

  7. Wow, what a difference an ocean makes. I had never heard of co-codamol and
    was excited to see that there was a new pain relief med for arthritis.
    Alas, it is just run of the mill Tylenol No. 3 which is codeine and tylenol.
    And the biggest side effect of codeine is constipation. The doc who follows
    you for your gut should be aware of both the constipation and your use of
    laxatives. There are varying types of laxatives ranging from industrial
    strength to milder stool softeners. It is easy to imagine that your
    stomach doc might prefer some over others and it is also easy to imagine
    that constipation might be equally as alarming.

    Your GP has given you amitriptyline for an 'off label' use. It is approved
    for depression but has been shown to help to with chronic pain, as well. In
    the states, it is seldom given for depression anymore because there are so
    many other antidepressants with fewer side effects but those haven't helped
    with long term pain. Frequently, it takes a couple of weeks to adjust to
    the older antidepressants and most patients do fine after a stuttering
    start. But, you can't take them for one day and determine your eventual
    tolerance of the medication.

    Here, many docs are using cox II inhibitors for arthritis with great
    success. I have no earthly idea what you might call them. You call
    acetaminophen 'paracetamol' and Tylenol No. 3 'co-codomol' and cookies
    'biscuits'. For that matter, you call elevators 'lifts' and pencil erasers
    'rubbers' (which got me into severe trouble when I moved back to the states
    after living in Australia where they have adopted your linguistic
    idiosyncrasies). Because they get at the cause of the pain, they are
    generally more useful. Also codeine is a mild opiate and people do tend to
    build up tolerance to it's pain relieving effect.

    If your heart rate is fine, I would blow off looking for answers from your
    cardiologist and go straight to the GP and rhumatologist. I would bring
    every single pill you take with you along with contact names and numbers of
    the docs who prescribed them so that drug interactions could be fully
    explored. Also, I have had some very dear patients who keep brief accounts
    of their medical history with their meds. This is invaluable when you only
    get a few minutes with a doc and you are nervous and in pain and likely to
    overlook something or not consider something to be important.

    It never hurts to eat well and exercise within your ability. It probably
    not cure your constipation but it may make it better.

    Chronic pain is serious. Many health care providers, including nurses, docs
    and therapists are quite capable of dealing with it. Others are not. Even
    in my own colleagues I see nurses look with disdain on someone who always
    'whines' about pain. And then I see them reassigned to a nurse who is very
    good with chronic pain and the patient does well. I have no idea how easy
    it is to change practitioners but I suspect there is greater relief for you
    available than you are currently receiving. Alas, I know regulatory matters
    like the back of my hand here in the states but couldn't begin to tell you
    how to navigate a system overseas. Good luck. Be aggressive. Deal with
    the pain and everything else will be much easier.

    j

    <[email hidden]> wrote in message
    news:[email hidden]...

    Quoted message said:

    I will try to give you and 'Complex' more info,as, in my first
    message, I was trying to be brief in case I repeat the stuff people
    have heard before. The last diagnosis I was given was paroxysmal AF
    and flutter and 2:1 AV block. The pacer is set to prevent my heart
    beat going below 60 or above 130. I need my pain meds for widespread
    osteoarthritis; neck, shoulders, spine, hands etc and the danger of
    dependency is something I am aware of. I take 4 painkillers each day,
    one co-codamol and one tramadol when I wake up and 2 co-codamol in the
    afternoon. I had three major procedures in a 15 month period ending
    last November. The first procedure was to remove a Duke's A tumour
    from my colon (outlook very good). It is now two years since that one
    and there have been no worrying symptoms. But, because my colon has
    had a large section section removed I tend to worry about using
    laxatives but I do use them as I am too uncomfortable otherwise.

    About two months ago I saw a rheumatologist and will be having a
    steroid injection in my shoulder - but, the appnt is not until Dec.
    This is the down side of our free National Health Service. My GP has
    given me amitriptyline (25mg) but it seems to interact with the
    verapamil i.e. I feel zombie like the following day so I stopped
    taking it.

    I do have good cardiologists. The 'chief' is a Professor who is said
    to be an authority on pacing. Unfortunately, there has been a big
    upset in our relationship. All his registrars are great but he seems
    to have a very high opinion of himself and I . As a result I am
    reluctant to ask for earlier appointments or leave messages with his
    secretary. (I suspect the Prof. resents the fact that my surgery was
    done at a different hospital..even though the new procedure I had for
    AF did not go well for me)
    It is possible I will be seen by a different consultant in future.

    Thank you both for your responses.
    Diana

    On Wed, 1 Oct 2003 21:01:07 -0500, "Julianne" <[email hidden]>

    Quoted message said:

    As far as verapamil and the pacer, it depends on what kind of pacer you
    have. It sounds like a run of the mill variety which first stimulates


    your

    Quoted message said:
    Quoted message said:

    SA node (causes the atria to contract) and then the AV (the ventricular
    counterpart). What these pacers generally do is prevent your heart rate
    from dropping below a certain point which is set by the doc. For


    instance,

    Quoted message said:
    Quoted message said:

    if your pacer is set at 72 beats a minute and your own heart rate falls


    to

    Quoted message said:
    Quoted message said:

    65, the pacer will recognize this and kick in to bring your heart rate


    back

    Quoted message said:
    Quoted message said:

    up to 72.

    What pacers do not do that verapimil does is prevent your heart rate from
    going to high. Even when pacers have a ramping feature which overrides


    the

    Quoted message said:
    Quoted message said:

    intrinsic rhythm or a defibrillator implanted with them, it is often
    unpleasant, although life saving, when they kick in. Therefore, it could


    be

    Quoted message said:
    Quoted message said:

    that your doc wants to protect you from both a low heart rate and a high
    heart rate. Neither are very good.

    You say that you really need your pain meds now. Why is that? There is
    nothing intrinsically painful about a rhythm problem.

    I have not heard of verapamil causing joint pain but most of my


    experience

    Quoted message said:
    Quoted message said:

    is in CCU. If you have long term chronic joint pain, regardless of the
    cause, it should be addressed by an ortho doc or a rheumotologist (if it


    is

    Quoted message said:
    Quoted message said:

    related to arthritis).

    Without reading too much into your post, I guess I am disturbed by all


    the

    Quoted message said:
    Quoted message said:

    attention to your pacer and the heart drugs, while you clearly state you
    'need' your pain meds. It is not unusual for patients with legitimate


    pain

    Quoted message said:
    Quoted message said:

    to develop a dependency on pain meds. Please forgive if I read too much
    into your post. There are chronic pain clinics that can offer you relief


    of

    Quoted message said:
    Quoted message said:

    joint pain. I have seen wonders worked with physical therapy. How much


    do

    Quoted message said:
    Quoted message said:

    you weigh? I lost twenty something pounds a few years ago because of my
    knees. Nothing else would motivate me. I still need to lose 20 or so
    pounds but damn if the joint pain isn't resolved!

    You need to be able to trust your doc. I know many cardiologists and


    heart

    Quoted message said:
    Quoted message said:

    surgeons. When I am called for advice, I always take into consideration


    the

    Quoted message said:
    Quoted message said:

    personality of the patient. I know a couple of docs that I don't
    particularly care for but if I code, I want them there. There are docs


    who

    Quoted message said:
    Quoted message said:

    really respect the patient's right to make an informed decision and go to
    great lengths to carefully lay out all their options and they don't fit


    well

    Quoted message said:
    Quoted message said:

    with patients who really don't want to know! So, without saying that


    your

    Quoted message said:
    Quoted message said:

    doc is bad, you may want to shop for another.

    Constipation is a minor problem unless you are the one suffering🙂 There
    are other remedies other than stopping meds. The best one I can think of
    eating well and exercising. The addition of fruits and veggies to your


    diet

    Quoted message said:
    Quoted message said:

    and walking would be good for anyone. If you change the amount of green
    leafy veggies you eat, you should call your doc and have your PT/INR
    checked. It is erroneous info that coumadin patients shouldn't eat green
    leafy veggies. Rather, the dosage should be adjusted to the patient's


    diet.

    Quoted message said:
    Quoted message said:

    For you, that means eating whatever quantity you desire on a regular


    basis

    Quoted message said:
    Quoted message said:

    and informing the doc if that changes. Yogurt keeps your gut healthy and
    there are some pharmaceutical remedies that help. Again, I worry that if
    you are taking pain medication with a sedative effect on a regular basis,
    your drive to exercise might be diminished.

    I wish you well. Please check back in. I apologize if I read too much


    into

    Quoted message said:
    Quoted message said:

    your post concerning your need for pain meds. It has never been and will
    never be my desire to have a patient hurting. Rather, for long term


    chronic

    Quoted message said:
    Quoted message said:

    pain, there are other answers besides pain meds.

    j

    <[email hidden]> wrote in message
    news:[email hidden]...

    Quoted message said:

    Few questions. . I have a mechanical MV and a dual chamber pacemaker.
    I have to take warfarin which I understand the reasons for but I also
    still take Digoxin and Verapamil. As far as I recall, digoxin
    strengthens the heart but with a pacemaker I am surprised that
    Verapamil is still necessary. I really need my pain meds now and
    would therefore really like to get off Verapamil because of the
    constipation problem. Also, has anyone who takes Verapamil noticed a
    worsening of joint pain?.

    Also, I am not being checked on as often since the pacemaker was
    inserted. It will have been 4 months next time I go to the clinic and
    after that I'm told its routinely 6 months for checkups. I can
    understand this for someone with a pacemaker who has not had heart
    surgery but thought it would be more often for someone like me with a
    leaking aortic valve and heart block etc. Appreciate any comments.
    Diana


  8. But, you can't take them for one day and determine your eventual

    Quoted message said:

    tolerance of the medication.

    I did take them again when I knew I didn't have to go anywhere the
    next day. Maybe I will try them again because the better sleep was
    great.

    Quoted message said:


    Here, many docs are using cox II inhibitors for arthritis with great
    success.

    Tried those (known as Cox 11s here as well) and stomach was affected
    so they are a no as far as the GP is concerned. I am on Warfarin and
    she is worried about bleeding.

    Quoted message said:


    Good luck. Be aggressive. Deal with

    Quoted message said:

    the pain and everything else will be much easier.

    You are so right with this, I just know it. But it is taking me a
    while to get there. Thank you for your good wishes.

    Bye the way, Tramadol may be called Ultram where you are. It gives a
    bit of a 'high' so is not much use before bedtime which is a good time
    to take pain reducing meds for arthritis.

    Diana

    Quoted message said:

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