Canadian Lyme conference coming

This just made me cry.  Bless her heart for being so brave.

 

 

I do applaud the U.S. government for moving forward with hearings such as this.  But it's just too slow of a process while young people such as this girl in the video, watch their childhood and teen years pass by. 

 

Canada will be hosting a Federal Framework on Lyme Disease Conference in Ottawa on May 16-17.  Read about it here.  This is required as part of the Federal Framework on Lyme Disease law that was passed a couple of years ago, spearheaded by MP and Green Party leader Elizabeth May.  Let us hope and pray that the message gets through to the health community.  Perhaps there will never be agreement between the two opposing sides in this controversy (IDSA vs. ILADS), but please, oh please, release doctors from the constraints and allow them to treat patients using whichever standard of practice they deem to be best for the situation.

 

Awoooooooooooooooo!



Today is a full moon.  But I probably didn't have to tell you that if you have Lyme.  Are you feeling worse today?  More neuro symptoms?  More fatigued?  More anxious?  I'm answering yes to all of the above.  I suppose that there is some strange relief in knowing that the cause is the full moon, and that I'm joined by countless others who are enduring this.

So yes, my Lyme has returned.  I'm having a bit of a relapse after having been antibiotic-free for 6 months.  Oh, how I was so enjoying the freedom of being pill-free!!!  But in December, my symptoms started to creep back.  To be honest, I had been neglecting the triad of good health:  eating well, sleeping enough, and exercising regularly.  It just got so busy in December preparing for Christmas, celebrating Christmas, cleaning up from Christmas, then writing report cards for the last 3 weeks.  I've been burning the midnight oil and eating too much gluten and sugar, which is just bad news all around. 

I've smartened up now, and am working on all 3 of these areas.  New Year's goals:  1) At least 7 hours of sleep a night  2) Eat grain-free and sugar-free (with the exception of one gluten-free starchy carb serving at dinner)  3) Exercise 3 times a week once I get my sleep stabilized.  Sadly, I'm back on antibiotics and have an appointment with my LLMD in a couple of weeks.

I noticed that I was feeling particularly bad this week and decided to check the calendar.  Yup...a full moon was approaching.  Do you believe in this full moon stuff?  It is not superstition, you know; it is science.  I have only to look at the behaviour of my students during a full moon to attest to the fact that the gravitational pull on the Earth affects us physically and mentally.  And it is certain that this phenomenon affects the reproductive cycle of Borrelia burgdorferi. 

I went in search of an explanation of this online, and found this interesting article which explains why we feel worse during the full moon, and sometimes the new moon.  Apparently, animals are sensitive to electromagnetic energy, and this includes microorganisms.  When the Borrelia sense the electromagnetic changes of these time periods, they are programmed to reproduce.  When they reproduce, there are obviously more organisms floating around your body.  The antibiotics are therefore killing off more bacteria than normal during this time, and you end up with a herxheimer reaction.  In other words, you feel crummy!  (Or let's say, crummier than normal.)

So there you have it.  You're not crazy.  It's a real phenomenon.  Do all you can to support your body and detox.  Drink plenty of water.  Add lemon to your water.  Take a detox bath.  Sleep.

Thinking of you all, and hoping you feel better soon.

Hello again, and welcome to a new year!

Well hello everyone!  Happy New Year!  I thought it was time for a new blog post; it's been a while.

I certainly don't post as much as I used to when I started this blog in 2012.  I was so on fire then, wanting to shout to the world everything I knew about this horrific illness.  I wanted to convince everyone of the TRUTH, and make known the inexcusable lack of knowledge in the medical community.  I wanted to change the system and change everyone's minds! 

Well, I doubt I've achieved much of those things through my humble little blog here, but I do know that I have been able to come alongside individuals and provide guidance, reassurance, and hope.  I know I needed that so very much when I was terribly sick with Lyme in 2011 without any medical explanation of what was wrong with me. 

I just want all of you Lyme sufferers to know that you are not alone in this.  So many people in Canada, the U.S., Australia, and Europe are travelling on this same journey, and it really is wonderful, in this age of technology, that we can connect and support one another through the rough times.  I am so honoured to be able to help you through this, via the stories and information on my blog. 

I am often reminded of The Starfish Story that I heard about 25 years ago, but which has always stuck with me.  I'll post it below.

Thank you for visiting.  And many blessings in 2016!

The Starfish Story

While walking along a beach, an elderly gentleman saw someone in the distance leaning down, picking something up and throwing it into the ocean.

As he got closer, he noticed that the figure was that of a young man, picking up starfish one by one and tossing each one gently back into the water.

He came closer still and called out, “Good morning! May I ask what it is that you are doing?”

The young man paused, looked up, and replied, “Throwing starfish into the ocean.”

The old man smiled, and said, “I must ask, then, why are you throwing starfish into the ocean?”

To this, the young man replied, “The sun is up and the tide is going out. If I don’t throw them in, they’ll die.”

Upon hearing this, the elderly observer commented, “But, young man, do you not realise that there are miles and miles of beach and there are starfish all along every mile? You can’t possibly make a difference!”

The young man listened politely. Then he bent down, picked up another starfish, threw it into the back into the ocean past the breaking waves and said, “It made a difference for that one.”

 

The Aftermath of Lyme

I've wanted to write this post for a while, but hesitated because I didn't want to discourage anyone who is going through Lyme treatment currently.  Frankly, the last thing I wanted to think about when I was in treatment, was how my life might be different once it was all said and done.  My focus was on getting well enough to be the wife, mother, and teacher I was called to be.  And those things I certainly achieved in the end.  Therefore, if you are in the researching phase, or just about to start treatment, or even in the thick of your regimen, please know that I simply want to share my experience and give people a taste of what the future might bring after the fallout.

Firstly, let me encourage you by saying this:  I have no regrets whatsoever for going through Lyme treatment!  Long-term antibiotics (4 years' worth!) literally gave me my life back!  I have just begun my fourth year of teaching post-Lyme, and some days I still marvel at the miracle of being able to do my job again, especially considering that I am on my feet all day and have very little time to give my brain a rest throughout the work day.  I cook meals, clean the house, shop, organize my family's social calendar, and chauffeur my kids.  Just like any other mom!  I am grateful, especially on this Thanksgiving Day.

What, then, are the bumps in the road?  What has Lyme left me with that I wish I could still overcome?  The following things are my personal experience, and I do not want to imply that everyone will travel the same path.  But I don't think that most people emerge from Lyme unscathed.  Here are my continuing issues:

1) Body pain!  Oh the annoyance of constant pain!  OK, it's not unbearable or anything, but the stiff muscles and sore joints are just constantly there.  When I get up in the morning, I feel like I'm 80 as I hobble to the bathroom.  My left hip and my feet are the worst.  Getting up from a chair after sitting for a while is not fun.  It takes a few minutes to loosen up.  Why is this happening?  Clearly, there is inflammation in my body.  In all honesty, my diet hasn't been clean lately, so this could be exacerbating the problem.  In an effort to help my body, I've decided to go grain-free and sugar-free for a time.  The first 4 days showed a marked improvement in my pain.  It was quite miraculous, actually.  I could suddenly move and bend without much pain, and the stiffness in the morning was reduced by about 70%.  I'm going to try to continue this regimen, with the hopes of adding back some grains (rice, quinoa) eventually.  I think I'll stay away from wheat, though. Wheat Belly has convinced me that I need to try to live without it.

2) The weight gain!  Oh my!  I really don't feel or look like myself.  My LLMD warned me that people often gain about 30 lbs in treatment.  Well, I've gained about 37 lbs since I started treatment.  Sadly, I did not heed his advice to give up sugar and simple carbs during my treatment.  Slowly, the weight packed on.  I should have listened.  For all of you out there in treatment.....If your doctor wants you to eat cleanly, perhaps sugar-free, wheat-free, or yeast-free, please do it!  It will help your inflammation and help to prevent the weight gain.  I am happy to report that giving up the sugar and grains last week resulted in a 3.5 lb weight loss.  I was very pleased, because frankly, you get to a point when you wonder if anything will work.  Knowing that this weight loss may take a year is daunting for sure, but I have to focus on all of the positives.....not just the weight loss, but the improvement in my skin, sleep, energy, stamina, digestion, etc.

3) The flare-ups.  From time to time, I still get little flare-ups of my symptoms.  There may be a night when I go to bed and the head vibrations come on, preventing me from sleeping.  Sometimes I'm just plain tired.  Sometimes, I feel my body vibrating or hear some tinnitus in my ear.  In the past, I would go back on antibiotics when these things happened, but now I'm more willing to see if the flare-up will subside.  It has done so the last few times.  This leads me to believe that I'm not having a true relapse, but rather some inflammation due to any number of things, e.g., diet, lack of sleep, illness, etc.  This is motivating me to get my inflammation under control through diet, better sleep, and supplements.

4) Supplements.  If you thought you could ditch the pill organizer after your treatment is done, think again.  I think it's important to stay on certain supplements that will assist the body in staying as healthy as possible.  For me personally, I am going to re-start Omega 3, B complex, alpha lipoic acid, vitamin C, iron, magnesium, digestive enzymes, and probiotics.  I've been off everything, including all meds, for a few months now.  However, I see the importance in resuming my supplements, so tomorrow I'll be re-filling my organizer.  Once again, a handful of pills will be my appetizer before every meal.

5) Emotional changes.  It is very strange to see parts of my personality change since my illness.  I used to be a Type A person all the way.  Now, I let things slide a lot more.  I had never been a procrastinator, but lately have been more prone to this.  I don't really have the same fear of illness or death that I used to.  I think it's because I feel that nothing can possibly compare to the hell I went through when I was sick.  It has hardened me somewhat.  I'm not sure if these changes are good or bad, but things are just different now.  Going through something so traumatic is bound to change you forever, in one way or another.

6) Coming to terms with the things I can no longer do.

- I can't skate!  I love skating; I even bought a new, good pair of skates.  But my feet hurt too much.  They start to ache after about 1 minute on the ice. 

- I can't eat sugar or grains. 

- I don't sleep as well.  Insomnia was one of the first Lyme symptoms I had.  Eventually, it got much better with the help of sleep meds, but I need to be very careful now as the sleep disturbances can come on suddenly.

- I have to say no to church and community activities because my body just can't handle it anymore.  I'm tired....a lot.  After working, caring for my family, and school work I must do in the evening, I need to rest.  And I'm not going to feel guilty about it either.

- I can't exercise to the same degree that I used to.  My body is just too sore.

7) Always being on the look out.  Unfortunately, I don't think that chronic Lyme can be cured....yet.  It goes into remission, but the stealthy bacteria hide deep in our tissues and organs.  Dr. Marty Ross, LLMD, believes that most people relapse within 5 years of going into remission.  Great.  I'm always wondering if my flare-ups are actually a relapse.  It's hard to know until you ride them out.  This means that at some point, I'll likely need antibiotics again.  Will my LLMD still be practicing then?  I don't know!  He is heading for retirement.  It's a worry I wish I didn't have.

Well there you have it.  The truth.  But keep in mind that this is my truth, and it won't necessarily be your truth.  Please don't worry!  Focus on getting better, but learn from my mistakes and be sure to eat right and exercise to tolerance.  Give your body all the tools you can to help it grow strong again once your treatment is done. 

Wishing you all the best!