Friday, March 29, 2013

Are You Exhausted? You May Have Adrenal Fatigue.



Adrenal fatigue is not generally tested for and treated in standard medical practice.  There are saliva tests that can be done to test cortisol levels accurately.  Most doctors do an AM cortisol, but I don't feel that the blood draw is accurate enough.  At the end of this post I will post a link to a quiz I found online that you can take yourself to see if you have symptoms of adrenal fatigue.  For now I'll describe what I've managed to store in my brain about the subject.

From my understanding, our adrenal glands sit right above our kidneys.  The adrenal hormone they produce is cortisol.  Cortisol is  essential to living.  Cortisol regulates all of our other hormones including the thyroid  and the sex hormones (testosterone, estrogen, progesterone, DHEA, etc).  If you have adrenal insufficiency, you most likely cannot stabilize your thyroid or sex hormone levels.  You feel exhausted and can't fight infections.  The list is enormous!



Here is another great explanation of adrenal fatigue:

Symptoms of adrenal fatigue:
  • Morning fatigue -- You don't really seem to "wake up" until 10 a.m., even if you've been awake since 7 a.m.
  • Afternoon "low" (feelings of sleepiness or clouded thinking) from 2 to 4 p.m.
  • Burst of energy at 6 p.m. -- You finally feel better from your afternoon lull.
  • Sleepiness at 9 to 10 p.m. -- However, you resist going to sleep.
  • "Second wind" at 11 p.m. that lasts until about 1 a.m., when you finally go to sleep.
  • Cravings for foods high in salt and fat
  • Increased PMS or menopausal symptoms
  • Mild depression
  • Lack of energy
  • Decreased ability to handle stress
  • Muscular weakness
  • Increased allergies
  • Lightheadedness when getting up from a sitting or laying down position
  • Decreased sex drive
  • Frequent sighing
  • Inability to handle foods high in potassium or carbohydrates unless they're combined with fats and protein
It's important to find a doctor or practitioner that A. believes in adrenal fatigue (they may only be slightly familiar with Addison's Disease) and B. is familiar with and knows how to treat adrenal fatigue.

I have confirmed hypoadrenalism via an extensive 30 day saliva test done by Genova Labs called Rhythm Plus.  I feel so lucky (and unbelievably grateful) that this $1000 test was covered by Medicare. It also tested my sex hormones and my melatonin levels.  Maybe I'll speak more on that later.  I am about to embark on Bioidentical Hormones starting in a few days.  Anyway, I knew it!  I suspected adrenal fatigue before Lyme, Mycoplasma, HHV-6, etc ever even came into my life.  I even hired Dr. Lam as my health coach to help me get past adrenal fatigue but the situation did not work out for me and it was costly and I didn't feel very helpful, so I gave up.

My primary care doctor (such a blessing to find down the street from my house) ran the saliva tests.  He does not find treating adrenal fatigue with cortisone to work out well for his patients.  He just wants me to stick with using herbs and glandulars.  Herbs such as licorice root, eleuthero root, and the glandular would come from bovine (cow).  It is basically the cow's adrenals.  Similar to people that take natural thyroid instead of synthetic.  It actually comes from the porcine's (pig) thyroid gland.  I was previously seeing a holistic practitioner who diagnosed my adrenal fatigue by using the tests mentioned on the Natural News website I have linked below.  He said my adrenals were "shot".

This is what my primary care suggested I take.


This is what I have taken in the past  and had immediate improvement.  I took it with the other one below.


You can click on these pictures and it will take you to Amazon site.

**You should always consult a practitioner before you take supplements or herbs.


Here is the link to the quiz that I promised you.  You can print it, and then take the quiz yourself and score yourself.  Bring the quiz in with you to your doctor or practitioner.



Here is a site that has great info that I got the other symptom list from: http://www.naturalnews.com/019339_adrenal_fatigue_chronic_stress.html

Good luck. To better health!!

xoxo Sonya


Saturday, December 8, 2012

A Little Inspiration

I saw this video and it inspired me to do a little yoga back in the Spring.  It's been making its rounds around Facebook lately, and I thought I too should share.  True inspiration.  For anyone.  Enjoy. Don't forget the tissues.


Tuesday, December 4, 2012

I Know I Need to Post an Update

I know I need to post an update. My laptop has took a final nose dive and is now in laptop heaven.  I have my handy iPad but its not great for typing.  I'll update soon and reply to comments at some point.  

I have not been doing so well since my surgery in June and in September I posted an update and I've been the same since.  Up until the past few weeks!  I'm starting to feel better again, more like pre-surgery. I even have a killer cold right now that has me up tonight with a fever of 101.2 and a racing heartbeat. I feel like death warmed over, but at least I know my immune system is working!  Right?

I'll post an update soon and now that I'm feeling better overall (well,once this cold is gone) I'll post the update, tell you about my new doctor.  I also want to tell you about a great nutritionist that has helped me a lot. She is on the other side of the US but we Skyped.  Check her out if you like www.supernaturalnutrition.net I'll give details later. Good stuffs. 

I didn't bail on you!

 Xoxo

-Sonya

Friday, October 19, 2012

Beyond Lyme Disease

Looks like Connie Strasheim is at it again.  I am so excited to read this book, let me tell you!  This is right up my alley and similar to what I have been focusing on since I stopped ILADS treatment for chronic Lyme disease.  I am so happy that someone with influence in our community took the time to right this book.  I have felt this way and have tried to help others to understand but I have been rejected, cast out, and turned away for having ideas other than KILL, KILL, KILL (killing spirochetes with antibiotics, etc).

Pick up this book.  I haven't got my copy yet, but from what I've read, this is the road.  Here is more info from the publishers site.  You can click the pic and be taken directly to the website.





Monday, September 10, 2012

My Two "Holy Grail" Supplements for Lyme Disease Recovery

I HAVE to promote this supplement!  Life Extension Super Bio-curcumin.  I ran out of this stuff about a week and a half to two weeks ago.  I've been taking one daily since last April (I think I started out taking one per day and moving up to two per day, one AM and one PM).  When my husband and I saw it during our last trip to Vitamin Shoppe, I pointed it out and said that I had just ran out of this, and I should buy some.  But I am trying to be frugal because I spend a lot of money on supplements and when you feel good, you think you no longer NEED certain things.  Well, I've been feeling pretty crappy for the past 10 days or so.  Started with just my right hand being in pain every morning and feeling head achy and blah.  Then moved to both hands and now my neck and shoulder pain is pretty intense all day, every day.  Also headaches from hell off and on, no energy, haven't been walking, doing stuff, etc.  Just haven't been "myself".  A couple of days ago, this stuff popped into my head for some reason, but I dismissed it (my body speaks to me, I just need to listen).  Then last night as I was trying to fall asleep, it came into my head again.  And I realized DUH!  This stuff helps my pain and inflammation!  Forget trying to save money, this stuff works!  My husband is on his way to Vitamin Shoppe as I type this to get it.  Can you say "HERO STATUS"?  I said to him, remember about 4 months ago when I ran out?  Same exact scenario. I had found it during an online search at Vitamin Shoppe (I was buying it online on Amazon or iHerb) I sent my husband to go get it.  It was our first ever trip to or purchase at a Vitamin Shoppe.  So while I was explaining to my husband how last time I ran out, I felt like crap and was in pain, blah blah blah and I found my review from back then (in May) on Amazon about how bad I felt after running out and we are going to try to find it somewhere local, no matter the cost.  

Anyway, I wanted to share this with EVERYONE!  I never noticed how much this stuff helped me until I ran out.  Same goes with the Liposomal Glutathione.  I didn't notice until I was out of it.  These two items I will never let myself run out of again!  I may try using Liposomal curcumin since this version is working so well for me.  Or maybe I'll attempt to make it myself.  I'm also going to post this on my blog.  Shouting it from the rooftops people!!!

So there you have it.  Super Bio-Curcumin and Liposomal Glutathione are my two HOLY GRAIL supplements that I will not live without.  So not worth it to save money.  My health and the way I feel is more important.

There is a reason for not just taking plain old glutathione or plain old curcumin (an extract of turmeric).  Apparently neither one of these substances are bio-available in our bodies.  Do a Google search on either one and you will see why I take them in these different, more costly forms.


You can find the Super Bio-Curcumin at a Vitamin Shoppe near you , they have GREAT prices.  Or you can find it online on Amazon.com or iHerb.com.  I made the links go straight to where you want to go.






Now in regards to buying Liposomal Glutathione (or even Vitamin C or Curcumin) I get that stuff from Let's Talk Health or from Amazon here it is on Amazon.  They also have a Liposomal version of Vitamin C.  I can make my own liposomal vitamin C and Glutathione, but I still purchase it from time to time when I can't find a good source of the pure forms of the two substances.

Friday, July 13, 2012

Near Death Experience?

Okay, I know.  The title is quite shocking, but I think this could be truly counted as a near death experience. You tell me what you think.  Be prepared, this is going to be a long post.

I've been having heart palpitations since I got sick.  Well, I've had them since I was 15, but intense ones since I got sick.  They have always bothered me and I often told my husband that I feared that my heart would just stop or that I would have a heart attack or something.  Always made to feel like I was overreacting, I didn't buy into it.  Neither did any of my doctors.  Let's see, I had told 3 LLMD's and my current primary care doctor about these issues.  With one of my doctors, I actually went to his office the next morning after an "episode" and told him I had a heart palpitation that lasted for about 20 seconds or some kind of something went on with my heart.  I asked for an EKG.  He listened to my heart, said it sounded fine, and that I didn't need one.   I was reassured, chalked it up to being a "hypochondriac".   Now that I think about it, my 2nd LLMD did order an echo cardiogram to make sure I was fine and did an EKG, so he didn't ignore it, I was just never referred to a cardiologist.  It is common with Lyme disease to think you are going to drop dead without a moments notice.  And it HAS happened to people.  WAY too often.

Anyway, I had 2 "events" or "episodes" about 6 or so months ago that really got me worried.  One while I was home alone with my teenage step daughter (the time I mentioned above) and another time when I was driving in a shopping center parking lot.  I felt it, it didn't end, and then I started to feel the strange blackness over come me.  It was similar to when I have fainted in the past, but not as intense.  I knew something was wrong and I knew it was related to my heart.  I thought, if I pass out here now, I could kill someone (people were crossing in front of me) so I rolled down my window and hit my E brake.  It passed and I carried on.  Went straight back to where I dropped my husband off for his haircut and told him something bad just happened with my heart and it is best that I stay off the road.

Being the drama queen that I am, that I KNOW I can be, I ignored it.  Until one morning, I woke up and my gut, my intuition, whatever you want to call it, told me to go see a cardiologist.  So I Googled "cardiologist", found one near me, Shiva Heart Center, called, no answer, they were out to lunch.  I'll call in an hour.  I forgot.  I would usually forget the whole thing, assume I was probably imagining these episodes or it was psychosomatic and just drop the issue.  But no, the next day I looked the place up again and called....

There is a reason I am telling you all this.  The reason is to TRUST YOUR GUT INSTINCTS.  You know your body better than anyone.  Had I not trusted my gut, well I would still be here now, but I may not be here a year from now.  Anyway, back to the story.....

They had a cancellation for the following day and offered me the appointment.  I made it and called my husband to make sure he could come with me.  I wanted him there to help advocate for me.  He had felt my heart beat irregularly before and now he too was a believer that something was truly going on.  We get there and the gal at the front desk tells me I need a referral and sent me away until they got approval, but waiting for the elevator, I was upset, I knew I needed to see this doctor today.  I told my husband, I'm going back in and I'm going to ask for the manager.  They saw me right away.  The doc was great.  Gotta love young doctors.  They seem "hungry" for finding the solution to your problem.  My primary care that first diagnosed me with Lyme disease, he was young and he wouldn't give up on me when several had.

Dr. Bhojraj said that he was going to order a Holter Montior for me.  It would stay on for 24 hours to 30 days.  He ordered an echocardiogram, an EKG, and a treadmill stress test.  These things would be spread out over the span of about a month.  The monitor was placed within a few days.  He told me that if we didn't see anything, he would implant a device that could stay for up to 3 years.  THIS DOCTOR BELIEVED ME!  Anyway, the monitor was placed and wouldn't you know it, no palpitations or other events.  I wore that thing around my neck and attached to my body for about 3 weeks.  I carried this cell phone that was part of the heart monitor system.  Very high tech, but also a pain.  It was there to alert the monitoring company if I needed an ambulance and it sent the data over the cell phone to the monitor company.  I told my mom and my aunt that I hadn't had any episodes and that it must all be psychosomatic and that I was "cured".  I must say I was a little disappointed that we didn't catch an event like I had had in the past.  I would move on and accept that my heart was fine, but in the back of my mind, I would always question what was going on.
Here is the cell phone that went with the holter monitor.  The heart would "beat" and the electrodes would beep and it would show me which electrode was not attached right or if I wasn't plugged in correctly.


This brings me to Thursday, June 28th, 2012.  I'm in bed, not feeling well at all.  I was going to push myself.  Here is my post on Facebook right before I got up:


Sonya
June 28 via mobile
Not having a good day so far physically. But I'm going to grab my boot straps. Or is it pick myself up by my boot straps. Whatever it is, I'm going to get off my fanny and go downstairs to feed my dogs and make my green tea latte. Then I hope to make it in the shower. I may not make it back upstairs, but we shall see :)


I got up and realized, I think I'm going to pass out.  I calmly hollered downstairs to my son (he is 16), "I'm going to pass out."  He said, "Ok."  I know he didn't realize what I meant.  Later he told me he thought I meant take a nap.  I then told him to call dad.  Then he knew, "Uh oh".  He had never been awake when I had anything bad happen to me.  The house phone wouldn't work, my husband had the main phone unplugged for the fax machine and forgot to plug it in. He came up and I had laid myself on the floor at the foot of my bed.  I've fainted plenty of times in my life and always prepare the poor person that has to witness me laying there unconscious.  Must be scary.  But I always tell everyone not to call an ambulance, just get me wet, cold washcloths and place them on my head, chest, etc.  I figured this was a fainting episode and perhaps a seizure.  I had plenty of time to tell him to get the washcloths and that I may have a seizure and that I was sorry.  I felt bad.  Out I went....
When I came to, I had no idea who I was or where I was.  Never has that happened to me.  I thought I had been drugged with a roofie or something.  That I must have been out at night (haven't been in years) and that I must have been drugged.  But then, who was I?  I felt someone rubbing my side.  Then I heard them speaking to me, telling me that I would be ok.  My vision was spinning, it was just like in the movies, I was trying to focus and then I turned and saw my son's face.  Only I had no flipping clue who he was.  No idea, he says when I looked at him, my eyes got really wide, and he could tell I had no idea who this guy was touching me.  It was sweet though, he said, "You'll be okay Sonya, you're okay" (he is my step son so he calls me by my name) as he was rubbing my side.  I recognized his voice before his face and once I realized who it was I relaxed and just laid there.  My husband was on his way and he told our son to call 911.  He had trouble apparently calling out on his cell phone as well.  But I heard the sirens and told him to lock the dogs up.  I also asked him to please put some sweats on me because I was in a short robe laying on my side in a ball.  He moved in record time.  I asked him if I had a seizure and he said yes, just a little one.  He said my whole body shook for about 3 seconds.  While laying there, my heart was going crazy.  Like a drum was being beating in my chest, it was pretty uncomfortable, and I thought, oh geez, I think I'm going to die now.  I was too weak to say anything.  I remembered that the cell phone to the holter monitor was up on my pillow. I was hoping it was catching this.  Little did I know that it was catching this and a whole lot more.
By the time everyone shows up, I'm a little embarrassed. I looked horrible and still had zit cream on my face!   They said I was really pale and asked my husband if I was usually that pale.  No.  They sat me up and I felt faint, so they laid me back down.  I told them I didn't want to go to the hospital, they wouldn't find anything wrong anyway.  They saw my holter monitor and I assured them that I was just wearing it to rule out any heart issues, not because I had any type of diagnosis.  Well, you wear one of these and you are going.  So off I went zit cream and all.  I asked if I could at least put on a bra and nope.  
In the ambulance, the electrodes from the heart monitor were in the way of what the paramedic wanted to do.  He wanted to take a picture of my heart.  Hmmm... apparently they can do that.  So I told him to just remove them.  While en route to the hospital, I hear another ambulance dispatched to my address.  The guys say, hey, that's your house, we were just there.  I told them it was probably because I disconnected my heart monitor.  But I must not have been thinking right because I had it disconnected every day for my shower.   Not sure why it didn't register.  I'll explain in a minute. The paramedic asked me what my normal heart rate was, because it was pretty low, it was at 50 bpm.  I said it is normally somewhere in the 60's.  Trust me, I know my heart rate.  I had issues with tachycardia before Lyme treatment and when I would have heart episodes, those episodes would have me checking my heart rate often. 
So I get to the hospital, they explain to the RN's that my chief complaint is dizziness.  They don't mention the passing out.  I found that odd, but I did tell the RN about it.  Syncope is I believe what they call it.  The ER doctor comes in and says he wants to do some blood work and check the enzyme levels of my heart, etc.  I'm thinking nothing and that they will send me home.  Then he comes back in he looks away from me and leans up against the wall.  Now I know, he was delivering bad news, but at the time, I didn't read his body language.  He says, "I just got off the phone with your cardiologist..."  I'm thinking, how did he end up on the phone with my cardiologist?  "You had a 20 second pause.  You had a 20 SECOND PAUSE!"  He wasn't shouting, but he was pretty animated and expressive.  I didn't know what that meant.  My husband didn't know what that meant.  He said that the holter monitor company also had called 911 after my son had because there is a delay in the connecting of the device I'm wearing and the cell phone (it updates every few minutes).  That explains the 2nd ambulance to my house. It recorded that there was 20 seconds where my heart didn't beat.  Was this a big deal?  Apparently so.  He said that I was being admitted and then he looked at me for the first time since he came back in the room and said, "You are going to the OR, you need a pacemaker."  That was the bad news his body was delivering.  He also said that they give pacemakers to people that have a 1.5 second pause.  So I was getting a pacemaker, end of story, period.  Don't think I had much of a choice.  I later learned that had I left the hospital without one, I would have had my driver's license revoked.  Good point.
I called my cardiologist and he said he was getting me the best surgeon to do this operation.  Dr. Lo is a Cardiac Electrophysiologist and that he does thousands of these operations every year throughout Southern California.  He said he didn't feel comfortable doing it because of two reasons.  I was young (most people with pacemakers are elderly) and because I was female and I was going to be wearing bathing suits and tank tops and he wanted to get me the best.  These pacemakers can be hideous looking.  I appreciated that and relaxed.  My husband's boss came to sit with me while we waited to find out details and I don't know how many doctors came in to look at me and say, "20 second pause?"  I'd have to ask her, but there was probably about 5.  Well, my heart apparently started beating again because it was young and healthy.  I still don't understand why it stopped in the first place.
Got my pacemaker that night and I must say it is a bigger deal than I thought it would be.  I stayed in the hospital over night and until the next afternoon.  They ended up placing the pacemaker under my chest muscle instead of under the skin.  Dr. Lo had told my husband after the surgery that I was too thin to have it placed under the skin.  So I would be in more pain and recovery time would be a bit longer.  But that I would be thankful later because of my age and that it wouldn't be as obvious when I wore tank tops, etc.  I appreciated that.  I found out a week later that I really had the Rep for the pacemaker company (Sara @ Medtronics) to thank for that.  I ended up meeting her last week at my cardiologists office.  She didn't recognize me but when she asked why had a pacemaker, that I was so young, I told her I had Lyme disease for a few years and that according to my cardiologist, the ER Physician (who used to see a lot of Lyme disease patients in the ER in Oregon), and the Cardiac Electrophysiologist this was due to the Lyme disease.  I ended up mentioning the 20 second pause and she looked up at me and said, "It was you?  I was in the OR with you.  Wow, a 20 second pause, well, you could of..... (now whispering) you could have died!"  I was reminded of this over and over again while I was in the hospital.  I didn't sleep much that night after the surgery and a couple of nurses came in to meet me, the "20 second pause girl".  Sara, the Rep told me that if she ever had to have a pacemaker she would choose Dr. Lo to do the procedure and that she was the one that talked him into putting it under my muscle.  She says she sees hundreds of patients with pacemakers per month and that I was so young and so tiny, that it would really be obvious and most likely both me.  She really went to bat for me.  So thanks to Sara!  When I asked my cardiologist what my diagnosis is he said, it is sinus arrest secondary to Lyme disease.
I did have a hard time coping with the pacemaker for the first several days.  I could feel it in me and it just effected me.  I cried a lot.  And I didn't feel well, and so I was afraid I had suffered a relapse of the Lyme disease.  I figured the surgery and anesthesia must have taken it's toll.  I ended up having some good days and Dr. Vinayak told me I had better appreciate, accept, and love that pacemaker.  So I have (I think).  My husband named it "Thumper".  It is the latest and greatest and it is MRI compatible which apparently is a big deal.  My extended family has really rallied around me and I think it has brought us closer together.  My sister, my nana, my aunt and my nieces have stayed in touch and continuously checked up on me.  My mom was out of town so she couldn't come help out during my recovery.  My husband works two jobs so my neighbor and some of my great friends came from a distance to sit with me while I would have otherwise been home alone and to help me eat, etc.  It wasn't the eating, but I couldn't dish out or serve my food with only 1 arm.  It was nice to be cared for.  My husband did THE BEST job and he tried not to stress too hard.  I had surgery a little over a year ago along with a 3 night stay in the hospital in Los Angeles and that was really hard on him.  So he did a great job.  We had help and I am so grateful.  Two nights in a row people from his office brought over dinner for us and it was great.  He even took me to my hair stylist to have my hair washed and blow dried for me.   I am so GRATEFUL!  I sent out cute thank you cards that I found at Trader Joes.
Thumper
I had my birthday a couple of days ago and here was my cake.  My mom really went all out and splurged!  I didn't make any plans with friends because I haven't been feeling back to my self and I didn't want to have to flake at the last minute and disappoint.  I live about an hour from everyone now.  So it was me, hubby, my son, and my mom.  My son had to go to work but the 3 of us went and saw the movie Ted.  I had to push myself, but I was so happy I went and didn't spend another birthday in bed or on the couch. 

P.S.  I should be trying out Synchronicity Wave System very soon at Dr. Vinayak's house.  I'll post once I try it out.  If I remember, we will do a video!  So stay tuned.  Here is some info on the system.  http://drchriskaufmann.com/main/synchronicity-wave-system/


Monday, June 25, 2012

Dr. Vinayak on a Talk Radio Show



Everyone knows I am a big fan of my "healer", Dr. Vinayak.  He was on the talk radio show In Short Order on Father's Day.  Dr. Vinayak is so willing to help others.  He does the conference calls with me and my friends every Wednesday (feel free to join us) to offer emotional support.  Every week, I am enlightened, inspired, and healed emotionally.  You would be amazed at how much our emotions effect our health.


A lot of people with Lyme disease had a stressful event preceding the symptoms of Lyme disease.  I was a complete stress ball when I came down with Lyme disease.  I was planning my wedding.  I have a friend who had a death in the family, another friend who was in a car accident, another friend who had just given birth.  The list goes on.  Our emotions can trigger temporary symptoms and temporary conditions.

Feel free to listen to the radio interview.  Keep an open mind :)

-Sonya


P.S.  You can click on one of the link below.  Or there is an embedded block floating around in this post that you can hit play on.


IN SHORT ORDER -- DR. VINAYAK

by In Short Order

in Health
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LET'S TALK LYME! LET'S TALK ABOUT THE STRESS OF LYME! LET'S TALK ABOUT COMBATING BOTH!



Listen to internet radio with In Short Order on Blog Talk Radio

Thursday, June 14, 2012

Great Advice

I took some notes from a conference call we had a few weeks back. Thought I'd share here.


Put away anything out of sight that reminds you that may have an illness. Supplements, medications, IV poles, etc.

Cells take information from thoughts. Emotions, stress or negative thinking is in the matrix or energy field surrounding the cell, responds to it. What you surround yourself with strongly influences your energy body or physical body.

If being in your environment reminds you of not feeling well (supplements, medications, etc). If that is in the environment, aren't you constantly being reminded that something is wrong?
If possible, find a way to get to nature. Backyard, grass, dirt, which is very healing. Kosher earth, the ground, will absorb a lot of info from your body and give you tremendous relief. Hug a tree. Bare feet on the earth. Allow the centers of your feet as anchors down into the earth and now you are very grounded. Your body finds alignment with the natural rhythms of mother earth. Your body finds it healing because it is the earths vibration.
The words we speak have an impact. The feeling behind the word is driving the creation or the manifestation.
Abraham (Abraham-Hicks) would say feeling is everything. (Here on my blog, there is an emotional scale that will help you choose feelings).
-Dr. Vinayak
www.electrumhealth.com