Welcome to my blog! This is a place of information and hope for fellow Canadians who are suffering from Lyme disease. I want to share with you the knowledge I have gained during my fight with this debilitating, frightening, and misunderstood illness. I hope you will be blessed.
Showing posts with label naturopaths. Show all posts
Showing posts with label naturopaths. Show all posts
Thursday, March 27, 2014
Lots of reading!
Way to go, Maclean's Magazine, for publishing a balanced article about Lyme disease. The more we can educate people, the more people will take precautions. After all, the best "cure" for Lyme is to never contract it in the first place. Click here to read the article in Maclean's.
On a personal note, I thought I'd give you an update about my life with Lyme. I stopped antibiotics around January 1 of this year, but re-started them a few weeks ago because symptoms started creeping back. On top of that, I caught the worst cold ever 2 1/2 weeks ago, and it's still hanging on. The cold, combined with the Lyme, has pretty much done me in the past 2 weeks.
Yesterday, I had the worst fatigue I've had in a couple of years. I came home from work, laid down on the couch, and could.not.get.up! Hubby had to make dinner, do the dishes, run our son to an event, make the lunches, and drag me up to bed! Thankfully, after a half-decent night's sleep, I'm feeling considerably better today, though still tired.
I'm trying to follow a detox diet currently, but I keep falling off the wagon! The book that inspired me is called The Detox Diet by Toronto naturopath Natasha Turner. Perhaps you've seen her on The Marilyn Show or Dr. Oz. The book is fabulous, and I have no doubt that following the diet would do wonders for my (and everyone's) health. So, I'll get back on it tomorrow and hopefully persevere a little longer this time. With Lyme disease, it is very important to control inflammation by eating a healthy diet free of sugars and low in starchy carbs.
I also purchased the book Why Can't I Get Better? Solving the Mystery of Lyme and Chronic Disease by MD Richard Horowitz. The book is much thicker than I realized when I ordered it, so it's not a quick read. It chronicles Dr. Horowitz's practice treating Lyme for the past 25 years with lots of patient stories as well as valuable medical information. If you have Lyme disease, it's worth it to have a copy of this hanging around for reference. Dr. Horowitz has quite a sense of humour which shines through in various parts of the book. Check out his Ballad of the Deer Tick on YouTube!
Hoping this post finds you well, with a happy heart despite circumstances. Spring is just around the corner (at least I think it is!) and I know I am looking forward to warmer days, sunshine, flowers, and the yearly reminder that new life can spring from a cold, dark place.
Labels:
books,
LLMD,
naturopaths
Wednesday, October 31, 2012
The cost of Lyme treatment
I've been wanting to post this for a while to give those of you who are just embarking on this journey some idea of what this is all going to cost you.
First of all, things may be different between the U.S. and Canada with regard to private insurance. I have read, for instance, that insurance companies in the U.S. will not pay for more than a month's worth of antibiotics because of the IDSA guidelines, but I have not found that to be the case with my insurance company in Canada.
Here is a breakdown of what you can expect.
Please note: These are the prices I paid in 2011. I know for a fact that some fees have gone up since then, especially for the LLMDs.
1. IGeneX tests - This will be one of your first expenses, perhaps before you even see a Lyme-literate medical doctor (LLMD). The tests will cost you anywhere from $200 - $1200 depending on what tests you order. The most important test for you to get is the Western Blot (both the IgM and IgG). These 2 tests will cost about $100 each. I chose to do the basic Lyme panel, all the co-infections, and the CD57 test, so my cost was around $1200. But don't feel that you have to do all of that! Some LLMDs don't even recommend spending the money on the co-infection panel because there are so many strains of these infections, but the tests only cover one or two strains. In all likelihood, the test will come back with a negative result for co-infections even if you are infected. Let your LLMD give you a clinical diagnosis for those. Sending your blood samples to California via FedEx will cost around $75. (See my IGeneX Lab tab for detailed instructions about sending your blood to this lab.)
Massage therapy - I never did this, but it is helpful for many people.
I know that when you start to add this all up, you might wonder how on Earth you will manage this. Take it one step at a time. Start with the IGeneX test and the diagnosis by an LLMD. You're looking at about $800 to get these 2 things done. Then, go from there and try to figure out how you might fit the treatment into your budget. You may need to cut some things out of that budget for a while: no new clothes, no vacations, no entertainment, no meals out, etc. You may be surprised at ways you can cut back to come up with the funds.
This is an investment in your future.
P.S. We're currently trying to have my Lyme expenses recognized by the Canada Revenue Agency for a medical deduction on our income tax. All of our receipts have been submitted, and now we're waiting. If we succeed, I will consider this a small victory for Lyme sufferers. Stay tuned....
(Update: Check out this post to find out what happened with the Canada Revenue Agency. Good news!)
First of all, things may be different between the U.S. and Canada with regard to private insurance. I have read, for instance, that insurance companies in the U.S. will not pay for more than a month's worth of antibiotics because of the IDSA guidelines, but I have not found that to be the case with my insurance company in Canada.
Here is a breakdown of what you can expect.
Please note: These are the prices I paid in 2011. I know for a fact that some fees have gone up since then, especially for the LLMDs.
1. IGeneX tests - This will be one of your first expenses, perhaps before you even see a Lyme-literate medical doctor (LLMD). The tests will cost you anywhere from $200 - $1200 depending on what tests you order. The most important test for you to get is the Western Blot (both the IgM and IgG). These 2 tests will cost about $100 each. I chose to do the basic Lyme panel, all the co-infections, and the CD57 test, so my cost was around $1200. But don't feel that you have to do all of that! Some LLMDs don't even recommend spending the money on the co-infection panel because there are so many strains of these infections, but the tests only cover one or two strains. In all likelihood, the test will come back with a negative result for co-infections even if you are infected. Let your LLMD give you a clinical diagnosis for those. Sending your blood samples to California via FedEx will cost around $75. (See my IGeneX Lab tab for detailed instructions about sending your blood to this lab.)
2. The initial consult with your Lyme-literate MD - This will cost you anywhere from $400 to $800. The New York LLMDs are more expensive for whatever reason. The NY LLMD that I saw charged $600 for the initial consult, whereas the Michigan LLMD that I go to charged $400.
3. Regular appointments with your LLMD - In my personal experience, regular follow-up appointments have been anywhere from $125 - $225 depending on how much time you spend with the physician. However, the fees will vary from doctor to doctor. Recently, someone told me that a doctor in Seattle charges $400 an hour! So, do your research. Some doctors will charge for e-mails, so keep that in mind. At the start of your treatment, you are bound to have some questions, and e-mails will be inevitable. Another thing to check out is how often your physician will need to see you. Mine wanted to see me in person every 6 weeks. Others require a visit in person every 6 months with a phone consult at the 3 month mark.
4. Travel expenses - Hotel, gas, meals. Don't forget to factor these things in.
5. Medications - Medications could cost up to $300 per month or more, depending on the medication. Some antibiotics are cheap because they have been around forever. Others are much more expensive. The treatment for babesia, a co-infection of Lyme, is quite expensive. Thankfully, my private insurance covered my meds right from the start. I still consider that a miracle and I'm so grateful.
6. Supplements - They probably cost
me about $100 - $200 per month. Some supplements are cheap, while others (e.g. good probiotics, alpha lipoic acid, Omega 3) can be quite expensive. Shop around. With some vitamins, your basic drug store variety is fine, but with other supplements, you will want to pay for a better quality pharmaceutical grade supplement. You'll need to research this and ask your doctor about it.
7. Other "paramedical" appointments:
Naturopath – Insurance covers
some, so I pay $35 every month or two.
Counselling - After insurance coverage, it cost $90 - $180 every month depending on how often I went. Very expensive, but very necessary! Find a counsellor who BELIEVES you regarding your Lyme diagnosis, and who will teach you how to deal with everything emotionally.Massage therapy - I never did this, but it is helpful for many people.
If you need to go a step further, you may want to consider finding a way to borrow about $10 000 - $15 000 which would hopefully cover your entire treatment (provided that your meds are paid for by insurance). Could you borrow from your line of credit? Would it be possible to sell one of your cars? These are just thoughts. I don't want to presume to know and understand anyone's personal financial situation.
But all this to say.....it WILL require some sacrifices! But it's for your health, and without that, you have very little. This is a situation that will hopefully end at a certain point in time. For me, it will have been a year and a half of financial pressure by the time I'm done treatment, but at least I'm now back to work and able to make a living and contribute to the family finances once again.
Thursday, September 20, 2012
Naturopaths could be our saving grace
The archived CBC News article below outlines the expanding role of naturopaths in Ontario. I learned today that effective March 2013, naturopaths here will be permitted to prescribe antibiotics to their patients. This is welcome news for Lyme sufferers! I believe that naturopaths will be much more likely to diagnose Lyme disease because they are not biased by the outdated IDSA guidelines. I believe they understand the Lyme situation at a much deeper level, and are more open to learning about it. They could be our saving grace! I just hope that they will not be constrained by the IDSA guidelines and investigated for 'unorthodox' use of antibiotics for Lyme disease cases. Then, we would be back to square one.
Update: It was explained to me by an assistant of Dr. Murakami that naturopaths have their own college which is different from physicians; therefore, they are not bound by the IDSA guidelines. The College of Naturopaths in B.C. has Dr. Murakami as their resource person for Lyme disease. I guess our Ontario College of Naturopaths will have to find someone to train and lead our naturopaths. Anyway, this was really good news.
Ontario just became the second province in Canada to get the green light for increased prescribing rights for naturopaths. British Columbia granted its naturopaths the right to prescribe a greater number of medications — as well as high-dose vitamins, amino acids, hormones, botanicals and herbs — in April 2009.
The announcement follows the granting of more powers to other health professionals, such as midwives and registered nurses.
On Oct. 20, the province's standing committee on social policy voted to amend Ontario's Naturopathy Act through Bill 179, allowing naturopaths in the province to prescribe, dispense compound or sell a drug listed in the regulations.
The bill is expected to be approved by the end of the year.
Though naturopathic doctors will still be restricted in the types of drugs they can prescribe, O'Reilly says they will be able to provide patients with medication they would otherwise have had to seek at walk-in clinics and emergency rooms. She says this decision will decrease ER wait times, and clear the way for speedier treatment for the acutely ill.
While the amendment increases the number of medications naturopaths can prescribe, it is far from being a carte blanche. Many drugs will still be off limits to NDs, such as psychotropic medications, including lithium, which affects the mind and emotions, and chemotherapy drugs. In B.C., these drugs currently can only be prescribed by physicians, said Christoph Kind, president of the British Columbia Naturopathic Association in Vancouver.
He says the list is still under review by the province's regulator, though he foresees acute-care drugs, such as antibiotics, to be included under the new prescribing rules.
Update: It was explained to me by an assistant of Dr. Murakami that naturopaths have their own college which is different from physicians; therefore, they are not bound by the IDSA guidelines. The College of Naturopaths in B.C. has Dr. Murakami as their resource person for Lyme disease. I guess our Ontario College of Naturopaths will have to find someone to train and lead our naturopaths. Anyway, this was really good news.
After extensive lobbying efforts, naturopaths across Canada are getting governmental green lights for greater prescribing rights.
Last Updated: Monday, November 9, 2009 | 4:51 PM ET
Anna Sharratt CBC News
Need an antibiotic for that nasty lung infection? Your naturopath may soon be able to prescribe it. That's because naturopathic doctors are among a group of medical professionals that are pushing for expanded prescribing rights — and they're recently seeing success.
Ontario just became the second province in Canada to get the green light for increased prescribing rights for naturopaths. British Columbia granted its naturopaths the right to prescribe a greater number of medications — as well as high-dose vitamins, amino acids, hormones, botanicals and herbs — in April 2009.
The announcement follows the granting of more powers to other health professionals, such as midwives and registered nurses.
On Oct. 20, the province's standing committee on social policy voted to amend Ontario's Naturopathy Act through Bill 179, allowing naturopaths in the province to prescribe, dispense compound or sell a drug listed in the regulations.
The bill is expected to be approved by the end of the year.
Drugs still require regulatory approval
The news is being welcomed by naturopaths across the country. "We see it as a very positive step," Shawn O'Reilly, executive director of the Canadian Association of Naturopathic Doctors in Toronto, told CBC News. "It will allow access to naturopathic doctors to prescribe drugs and supplements formerly off limits."Though naturopathic doctors will still be restricted in the types of drugs they can prescribe, O'Reilly says they will be able to provide patients with medication they would otherwise have had to seek at walk-in clinics and emergency rooms. She says this decision will decrease ER wait times, and clear the way for speedier treatment for the acutely ill.
While the amendment increases the number of medications naturopaths can prescribe, it is far from being a carte blanche. Many drugs will still be off limits to NDs, such as psychotropic medications, including lithium, which affects the mind and emotions, and chemotherapy drugs. In B.C., these drugs currently can only be prescribed by physicians, said Christoph Kind, president of the British Columbia Naturopathic Association in Vancouver.
He says the list is still under review by the province's regulator, though he foresees acute-care drugs, such as antibiotics, to be included under the new prescribing rules.
Labels:
alternative medicine,
hope,
medications,
naturopaths
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