Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Doctors Prescribe Respidol


Serversymptoms

Recommended Posts

Serversymptoms Contributor

DRUG IS RISPERDAL, NOT RESPIDOL.

I recently went to the doctors and was given the following test:

Test

CBC (inc. diff + plt) [L]

Profile

Comprehensive panel [RB]

Miscellaneous test

Blood C & S with ARD

(To answer my question about the test refer to this link :https://www.celiac.com/gluten-free/index.php?showtopic=60247)

_________________________

On top of giving me the test, I have been prescribe .25 Respidol, every 12 hours... and told by the doctors that I can either take it at home or I will be place in a hospital ( moved from Lansing to Grand Rapids) where they will make sure I'm taking that medication. I told my mom ( I'm 17 years old) that I don't want to take such, and recently I have only been talking about improvements of symptoms I've had. I don't see how one would be force to take medication just because they talk about their health problem and figured out what it is. I do suspect base off the test they may find my health problems or at least be alerted ( to know what health problems I'm talking about, need to see the link) and I will immediately be removed from such medication.

Though just as of now I really do not want to take respidol, I've read nothing but horrible things on the drug. Do I really have to take such medication or be force to take it... isn't that beyond ones own rights? I even try to stay away from tylenol as much as I can, or any medication for colds ( I do experience runny/ stuff nose sometimes etc... but never been sick with a fever since almost forever) etc... ( unless a must vacine), why would one think taking respidol would be okay for me? Just imagening the side effects is enough for me, though I do suspect if my candida was diagnosed I will be given a perscription to dianogse the candida... and most will experience die off side effects, which is okay to experience.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Rissmeek Newbie
DRUG IS RISPERDAL, NOT RESPIDOL.

I recently went to the doctors and was given the following test:

Test

CBC (inc. diff + plt) [L]

Profile

Comprehensive panel [RB]

Miscellaneous test

Blood C & S with ARD

(To answer my question about the test refer to this link :https://www.celiac.com/gluten-free/index.php?showtopic=60247)

_________________________

On top of giving me the test, I have been prescribe .25 Respidol, every 12 hours... and told by the doctors that I can either take it at home or I will be place in a hospital ( moved from Lansing to Grand Rapids) where they will make sure I'm taking that medication. I told my mom ( I'm 17 years old) that I don't want to take such, and recently I have only been talking about improvements of symptoms I've had. I don't see how one would be force to take medication just because they talk about their health problem and figured out what it is. I do suspect base off the test they may find my health problems or at least be alerted ( to know what health problems I'm talking about, need to see the link) and I will immediately be removed from such medication.

Though just as of now I really do not want to take respidol, I've read nothing but horrible things on the drug. Do I really have to take such medication or be force to take it... isn't that beyond ones own rights? I even try to stay away from tylenol as much as I can, or any medication for colds ( I do experience runny/ stuff nose sometimes etc... but never been sick with a fever since almost forever) etc... ( unless a must vacine), why would one think taking respidol would be okay for me? Just imagening the side effects is enough for me, though I do suspect if my candida was diagnosed I will be given a perscription to dianogse the candida... and most will experience die off side effects, which is okay to experience.

Can I ask why they put you on the medication? Your symptoms and the medication do not go hand in hand. I know the medication very well and yes it is 100% possible that they would/could put you in the hospital to make sure you take it. It's a safety measure. Also depending on what state you live in, you are still a minor meaning that your parents would be the ones making your medical decisions.

Serversymptoms Contributor
Can I ask why they put you on the medication? Your symptoms and the medication do not go hand in hand. I know the medication very well and yes it is 100% possible that they would/could put you in the hospital to make sure you take it. It's a safety measure. Also depending on what state you live in, you are still a minor meaning that your parents would be the ones making your medical decisions.

I have no ideal either why they would put me on risperdal. Lately the only thing I have been mentioning to my mom is improvement in symptoms since removing yeast, and how I also think I have candida ( even tested positive for spit test) and was able to invade in me being gluten intolerance. I do not want to take such medications, as I've mention I even avoid taking tylenol when I get headaches. I'm not a threat to anyone or myself all I do is mention my symptoms and how I know it's not in my head. I live in Michigan, I'm 17 years old.

So it's possible that they cant force me simply if my mom say ....his health has been getting better, and I feel as well as he that this medication is not needed.

Serversymptoms Contributor

IM NO LONGER LOOKING FOR ANSWERS TOWARDS THIS QUESTION

I have not been taking this drug at all, and after my blood results came back it now seems that I'm no longer being influenced to take it by anyone. I think now they will start looking into my health.

ravenwoodglass Mentor
IM NO LONGER LOOKING FOR ANSWERS TOWARDS THIS QUESTION

I have not been taking this drug at all, and after my blood results came back it now seems that I'm no longer being influenced to take it by anyone. I think now they will start looking into my health.

I am glad to hear that they are taking your health issues a bit more seriously. Do you know what the blood test results were? I had not answered previously but when this medication is prescribed for a genuine need for it it can be a big difference. It is not however something that should be given without a doctor being absolutely certain that it is needed IMHO.

Serversymptoms Contributor
I am glad to hear that they are taking your health issues a bit more seriously. Do you know what the blood test results were? I had not answered previously but when this medication is prescribed for a genuine need for it it can be a big difference. It is not however something that should be given without a doctor being absolutely certain that it is needed IMHO.

Yeah I'm really glad they lifted off that medication, for I don't need any at all. It was all just a really horrible moment, and still shock with the doctors actions. Well there were a few things ( about 4 or 5 ) below or above the normal range. Though basically it was C02 above average ( 32) and white blood cells below normal ( 2.9).... Yeah I know the ranges are not exotic like 1, .5 etc... but this should still aware them of a health issue I have and speak of.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.