So there are a few things I will be trying in the next months to see if I can improve my pain, stiffness and fatigue myself vs. trying more medications. I'm just not much of a medications kind of person, especially since I'm seeing no results and feel like what's really happening is just masking the problems with more problems.
Here's what I have started -
Chiropractic care. Now, this is not necessarily new, I have used chiropractic care sporadically for years. However, what I am trying now is to use it regularly and to also talk to my chiropractor about my diet, supplements and other alternatives.
Chiropractors are much more than just "bone snappers." They really do have a vast amount of knowledge on alternative therapy. Your mileage may vary depending on whom you choose as a practitioner. But, i recommend trying it, it does seem to really help some of my pain, especially in my neck and hips.
More information about proper body alignment and health can be found here -
How Chiropractors Benefit Your Health (Via Fox News 2012)
Mayo Clinic Basics on Chiropractic Care
Another good explanation of Chiropractic Care (Alive has lots of information on natural health & wellness)
The other thing I am incorporating into my diet right now are essential fatty acids, in the form of Fish Oil Supplements. I talked briefly about this in another blog post. But here is some information on this supplement as well as a few other things that can naturally help your body fight joint pain & inflammation as well as boost your immune system.
Fish Oils (from Arthritis Research UK)
Omega-3 Fatty Acids (University of Maryland Article - talks about many diseases Omega-3's can help)
So that's where I am at right now. Chiropractic care & fish oil for now. Researching many more supplements, diet changes & lifestyle changes. So please stay tuned and SHARE this blog with anyone you think may benefit from this information, that's why I started it ;-)
Sarah
Showing posts with label inflammation. Show all posts
Showing posts with label inflammation. Show all posts
Thursday, February 20, 2014
Thursday, January 16, 2014
Treatment Topic Thursday ...
Thursdays I will devote to talking about treatments, both conventional and unconventional. I will try to go in detail of each topic and hopefully you will find the information helpful. If there is a topic you would like me to research and post about I'd be happy to try to do that, just message me.
Today's topic is Plaquenil (Hydroxychloroquine). This is the first try drug for RA according to my doctor. They start here because it is the least likely of the RA treatment drugs to cause side effects. The interesting thing about this medication is that it's actual original use was as an anti-malarial drug.
It's used to treat the inflammation of both RA and Lupus.
Possible side effects -
abdominal cramps, diarrhea, heart problems, reduced appetite, headache, nausea & vomiting, altered eye pigmentation, acne, anemia, bleaching of hair, blisters in mouth and eyes, blood disorders, convulsions, significant vision difficulties, diminished reflexes, emotional changes, excessive coloring of the skin, hearing loss, hives, itching, liver problems or failure, loss of hair, muscle paralysis, weakness or atrophy, nightmares, psoriasis, reading difficulties, tinnitus, skin inflammation and scaling, skin rash, vertigo and weight loss
That huge list of side effects doesn't exactly seem "mild" to me. I have been on this drug now since my diagnosis in October. I have noticed no improvement in my symptoms as of yet though I was told improvement should be noticed in 6-8 weeks. My dose was increased in November after being on it for 6 full weeks. Still, no improvement has been seen. At my recent appointment i discussed with the doctor that I am seeing no improvement with all the drugs they have me on, including this one. In fact, I am feeling worse. She added another drug to my "cocktail" and wants to see if this one will help the others also work better. So, when i go back in February we will consider which drugs are or aren't helping and again adjust.
For me this is the frustrating part of being at the beginning of this process. A large list of medications to take daily, side effects you aren't sure are coming with this drug or that drug. And continued pain to the point you don't think ANY of it is helping.
Trying to stay positive is definitely an UPHILL battle for me right now. I pray daily for answers, for pain relief and for strength to do the things I have to do. This little saying was posted on Facebook the other day, it accurately describes how i feel many days lately.
Today's topic is Plaquenil (Hydroxychloroquine). This is the first try drug for RA according to my doctor. They start here because it is the least likely of the RA treatment drugs to cause side effects. The interesting thing about this medication is that it's actual original use was as an anti-malarial drug.
It's used to treat the inflammation of both RA and Lupus.
Possible side effects -
abdominal cramps, diarrhea, heart problems, reduced appetite, headache, nausea & vomiting, altered eye pigmentation, acne, anemia, bleaching of hair, blisters in mouth and eyes, blood disorders, convulsions, significant vision difficulties, diminished reflexes, emotional changes, excessive coloring of the skin, hearing loss, hives, itching, liver problems or failure, loss of hair, muscle paralysis, weakness or atrophy, nightmares, psoriasis, reading difficulties, tinnitus, skin inflammation and scaling, skin rash, vertigo and weight loss
That huge list of side effects doesn't exactly seem "mild" to me. I have been on this drug now since my diagnosis in October. I have noticed no improvement in my symptoms as of yet though I was told improvement should be noticed in 6-8 weeks. My dose was increased in November after being on it for 6 full weeks. Still, no improvement has been seen. At my recent appointment i discussed with the doctor that I am seeing no improvement with all the drugs they have me on, including this one. In fact, I am feeling worse. She added another drug to my "cocktail" and wants to see if this one will help the others also work better. So, when i go back in February we will consider which drugs are or aren't helping and again adjust.
For me this is the frustrating part of being at the beginning of this process. A large list of medications to take daily, side effects you aren't sure are coming with this drug or that drug. And continued pain to the point you don't think ANY of it is helping.
Trying to stay positive is definitely an UPHILL battle for me right now. I pray daily for answers, for pain relief and for strength to do the things I have to do. This little saying was posted on Facebook the other day, it accurately describes how i feel many days lately.
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