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Curing Allergies: Advanced Allergy Therapeutics

I’ve spent several days, weeks even, trying to compose this article.  Each time I think I have it, something happens that makes it even better.  At this point, I’m almost overwhelmed by all I want to say.  I’ll do my best to put it into words.  But just how does one describe something that seems so… miraculous?

I think I’ve always been ill.  I have had flashes.  Moments.  There were even entire days and maybe weeks (although that might be stretching it a bit) while Brian and I were traveling.  Mostly, they were moments so sublime that they dragged me out, beyond the haze and the pain, into so much blinding wonder or joy that I couldn’t help but let myself get lost in them.  When Brian proposed, one Christmas morning, on one knee in front of his parents and sister, I was lost in so much sheer excitement and joy – of course I bounced everywhere for the rest of the day.  When I saw my uncle all dressed up and ready to walk me down the isle, I was swept up in the moment and never came down off that cloud my entire wonderful wedding day.  There were days at a time while we traveled across the country in our overpacked motorhome that I was so absorbed by the beauty of majestic mountains, winding rivers, and dramatic plateaus that even the pounding sinus headaches or the gut-wrenching abdominal pains couldn’t hold me back from trying to soak in as much of it as I could.  And, when I held my precious little baby boy in my arms as he gazed up at me with those big beautiful blue eyes – nothing could distract me, save the tears of overwhelming joy that this little person had chosen me to be his mother.

But these were moments.  What about all the rest of the time?  It seems like so much of my life has been shrouded in pain.  Physical and emotional.  The last seven or so years, since becoming pregnant, have been a steady decline.  It’s as if the process of giving life was draining mine away in turn.  The physical drain of bearing children and then spending several months immediately afterwards not really sleeping had sent my body into a spiral downwards.  Emotionally, I began slipping.  I had detoxed myself just before getting pregnant, in order to purge smoking out of my habit list.  I’d promised Brian – and myself – that I wouldn’t smoke anymore if we were going to have kids.  We were ready, so I quit.  In the process, I had researched some herbal assistance to cleanse some of the toxins out of my body.  I had never felt better.  I’d even gotten back to very near my ideal weight.  Then pregnancy, and gestational diabetes, seemed to throw me out of whack.  Despite the fact that I started eating better than I ever had before, no amount of green veggies was going to work at that point.  The downward track had begun.

Fast-forward to December, 2009.  I have a disc, collapsing in my back.  While the back pain for that seemed to have gotten better after a year of working out and doing exercises from a physical therapist, the knee pain I’d originally gone to the doctor had not only gotten worse, but is now in both knees.  My Irritable Bowel Syndrome, diagnosed just before I was married in 1997, was once again worsening.  I’d had my first colonoscopy, but nothing appeared to be wrong, so the diagnosis held.  I’d begun seeing a Rheumatologist, who diagnosed me with Fibromyalgia, a cronic pain disorder.  To me, Fibromyalgia has been my body’s way of screaming out to me for help.  Yet, what could I do?  Every doctor I saw wanted to put me on more medication, until I was taking eight different prescriptions.  It would have been ten, but the cardiologist agreed to wait and see if the fibromyalgia treatment worked before trying anything for my high blood pressure and cholesterol.  I was watching my diet, but the cholesterol wouldn’t go down, the blood pressure stayed (I’ve always been a low-salt kind of girl!), the old hiatal hernia (diagnosed back when I was a high school junior) started acting up and I was on something for reflux as well.  The allergies themselves were slightly better managed by the new prescription of Singular, but I was supplementing Benadryl on a regular basis still, and both Tylenol and Tums were regular visitors too.  I finally saw an eye doctor to try and solve the splitting headache pain that was now centering on my left eye, but she firmly explained to me that my eyes were in great health, but I was clearly under a lot of stress…

In fact, nearly every doctor I saw either said I was in perfect health and should not be experiencing the pain I was (desperately) trying to describe to them, OR… that they only ever saw “this kind of degredation” in “older” or “geriatric” patient.

Geriatric?  Great.  So I have half my doctor’s trying to tell me to “manage stress better” and shaking their heads as if I were a hypochondriac, and the other half worrying over me as if I was prematurely tipping headlong into an early grave.  And, frankly, with the way I felt – my money was on the latter.  If it weren’t for my beloved husband and my two beautiful children – and that knowledge that I had a wonderful thing going on there… well, I don’t know that I wouldn’t have just given up entirely.  There wasn’t a week that passed where I didn’t cry at least three-four times.  Possibly more.  Not just a wispy tear here or there, but deep-down, shuddering, hold-myself-together-with-both-arms-or-I’m-going-to-shatter-and-I-don’t-know-what-happens-then kind of crying.  I was adrift with despair, and Brian and the kids were the only real raft I had left that I could be sure I could rely on.

Because, when you’re there, nobody but family (and even then, only the closest ones) wants to get too close.  You’re a sinking ship and part of them can sense it, like a strange whining noise off to one side in the back of their heads.  So you hold on as best you can and ride through it all, just trying to keep enough above water so you don’t stop breathing.

I was in so much pain.  Physical pain.  Sure, I was under some stress, but damnit – so were other people around me!  How could THEY manage to get through it, if it was normal?  Is this how everyone feels?  And, if so, how could these other moms around me not just lay down and die???  There were days it hurt so much that a part of me wanted to.  Fortunately, I had my beautiful little family.  I wanted to get better.  To be a better me, so I could be better for them.  So I kept plodding along, to each and every damned doctor appointment.  There were little glimmers of hope along the way, but each one that didn’t FIX anything just brought me a little further back down the slope in the end.

And then one day, out of the blue, Brian sends me an email:

This was advertised in the Aspectarian.  Their theory sounds good but I’m skeptical about the methodology.  I tried googling for independent reviews of it but didn’t find anything useful at a quick check.

 http://www.midwestallergyrelief.com/

 It would be nice if it’s everything they claim, but I have doubts.

 Anyway, thought I’d share.

Brian doesn’t send me crap in my inbox, mind you.  He knows I already get something like 100 emails a day that just end up getting deleted after a glance over the titles.  I don’t have time for nonsense – I get too overwhelmed – so, naturally, I click the link.  He’s “skeptical”, but he’s sent it anyway, so it bears at least a glance…

Twenty minutes or so later, after having perused the site and watched the video of a news report they have there, I call him at work.  This is a VERY close approximation to the conversation that followed:

How much did you look at?  Do you know what they are saying?” I ask him.

I didn’t have time to look too much, and I can’t watch the video at work,” he tells me.

I think I want to try this,” I tell him.  Then the tears start welling up in my eyes.  “No, I HAVE to try this.  They say they can CURE allergies, Brian.  CURE them.  I don’t know… I’m skeptical… but if it WORKS… I think I have to try.  If it DOES work, and I DON’T try it… I can’t… I need to try this.”

So… make an appointment,” he says.

Are you sure?  I mean… we can’t afford it right now.

We’ll spend more than that in copays this month as it is, based on what we’ve been spending.  Nothing else has worked, and it can’t hurt to try.  Just make an appointment and see what it’s all about and we’ll take it one step at a time.  If you want to try it, then let’s do it.”

Have I mentioned lately how much I love my husband?  So.  Very.  Much.

I called them within about ten minutes or so after that.  I didn’t want to lose my nerve.  I was still skeptical, myself, you see.  Still so very wanting to believe that they could do what they say, but really – doubting it.  But I couldn’t risk not trying.

My first appointment was January 7th, 2010.  By January 20th, we’d confirmed we could use the money in the health spending account to cover it (since Brian had set one up after we’d had SO MANY doctor’s appointments the prior year) and that evening Brian and Jareth had their first appointment.  The next day, January 21st, Kayla had hers.  Within ONE WEEK, I could tell that there was a difference.  Within ONE MONTH, I had gotten to a point where I had realized that I had energy equivallent to when I was in college, AND I had successfully weaned OFF one of my fibromyalgia medications AND cut the medications for my Irritable Bowel Syndrome in half.  TODAY, I called and asked to have the packet to wean down off of one of my other fibromyalgia medications as it is giving me TOO MUCH energy.  At this point, even when I’m NOT under the influence of that particular medication, I feel like I have more energy than I have ever had in my entire life.  Maybe when I was a child, back before I can remember…?  Maybe I had this kind of energy then?

Don’t get me wrong.  The knees still hurt, so I’m not giving up a couple of my meds just yet.  There’s a different kind of problem there.  I’ve also noticed other things.  I had a head injury back in July of 2001.  The swelling to my brain didn’t end until they were at the point where the next step would be drilling a hole to drain the fluid.  Five days in ICU, ten days in the hospital total, with months of seizure meds and follow-ups.  The swelling crushed my olfactory nerve, and one day I realized I’d lost most of my sense of smell as a result.

Nope.  What I’d lost was the ability to smell the finer details, clearly.  Or maybe, the body CAN heal that after all, despite the surgeon saying that it was likely to be permanent.  Over the last two months, I have gained nearly all my sense of smell back.  Because I’ve gotten rid of so many allergies… I can breathe again.  And those were mostly FOOD allergies – we’re just getting into the pollens and respiratory stuff.

The treatment is relatively painless, they say.  After two years of allergy shots with no results, I can attest to that.  With the shots, every other Monday night was my own personal hell.  I wanted so badly for them to work that I was all but lying to the ENT nurses – telling them that the side effects I was experiencing were less than they really were because I had already been sent back to the starting point once.  “Shots night” meant we met at a clinic so Jareth, Brian and I could all each have one shot per arm, which left us burning at first and then bruised later on.  I would get a serious headache, dizziness, and fatigue.  And then – I couldn’t sleep.  Every other Monday night was one where I would toss and turn and then have brief bits of sleep where I’d wake up from nightmares and not get any rest at all.  And, two weeks later, I’d have to go do it again and pretend (mostly for Jareth’s sake) that everything was going great.

That was every two weeks.  Once I realized what this was going to do for me – I started scheduling as many appointments as I could.  A few times, I even had two in one day, with a two-hour break in between.

I won’t say there haven’t been side effects to these treatments, however.  There have been points where my body was detoxing so much I would just suddenly need to lay down and sleep.  I could tell my body was going through something.  And I started to realize early on that my body was communicating with me more and more through the process.  One of the two doctors who administer the treatment described it to me as an “onion” effect.  With each new allergy/sensitivity that was resolved, my body was better able to notice and communicate the other problems.  There was a point, about one month in, where I began to feel like I might have a clue about what it felt like to go through chemotherapy – there were points where I felt the way my mother once looked when she was going through chemo.  I cried and cried, and slept as much of it off as I could, while my body grappled with trying to tell me about EVERY DAMNED PROBLEM THAT EVER WAS, as it pertained to my health.

Please remember that I was (and still am) going EVERY DAY.  Results not typical, unless you are going to fanatically try to get better as FAST AS FREAKING POSSIBLE, like I am.  Most people could probably do this once per week and their body would have more time to adapt and adjust to the new input.  But, at this point, you know I have been both desperate and used to the “no pain, no gain” philosophy.  And it was working!  No WAY was I going to slow down!  I still haven’t yet. 

Then they treated me for EMOTIONS.

That’s right folks – certain emotions, like Anxiety and Sadness, were literally giving me physical problems.  THIS was the “critical mass” point for me.  I’d been feeling crappy all week, like I was fighting something off.  I wasn’t sure if I was sick or if I’d just been overdoing the treatments, but I was leaning towards “sick” based on nearly throwing up Tuesday morning.  Brian had stayed home that day and I’d skipped my treatment.  On Wednesday, I dragged my still-waning self into the office to get the treatment in.  On Monday, I’d been having a discussion there about what exactly a treatment for emotions might help with.  We’d talked about it in relation to Jareth, but on Wednesday, (oh yeah, this is LAST Wednesday, folks) I went in and suggested we do that one for ME instead.

I started feeling a little different before I’d even left the office.  By Thursday evening, I was euphoric.  I had never felt so good in my LIFE.  I was grinning ear-to-ear and telling everyone I could catch the ear of…

The web site.  Go there.  Look at it.  It WORKS.  Here, I’ll link it again, to make it more convenient: 

 http://www.midwestallergyrelief.com/

There’s so much more that I can, and will say about this.  In the last four days I have possibly accomplished more than I have in the prior four weeks towards tasks that have been sitting in my inbox for months.  My energy is better.  My focus and alertness have improved.  I am absolutely amazed at what they have been able to do for me in such a short period of time.  The results are dramatic and phenomenal!

I will continue this in a future post.  I want to talk about the treatment itself – how it works.  I want to tell you how the kids have responded.  I’m hoping to encourage Brian to post his own results on his web page as well, since he has to schedule his appointments in the evenings and is taking the process more slowly than I am.  I want to tell you about the great people I’ve met there, and how different an experience it has been than the cold, dry medical world I’d grown accustomed to.

Stay tuned.  More to come as I have time!

Bunny Photo Shoot #1

click to view larger

click to view larger

For some reason I like this picture best out of the mini photo shoot Kayla and I did this morning with Snowflake.  He and I have been coming to terms.  Clearly he likes his cage a.  particular.  way.  Thus, the litterbox has swapped corners with the toy corner, I have moved the hay hanger and bin from the back to the front of the cage, and today I removed the food dish that he kept flicking all the food out of before eating it and instead put in one of the very bowls you see in the picture above.  He also gets his salad served to him on a matching white rectangular plate these days.  Perhaps he just likes to color coordinate all his dishes with his fur, or perhaps he just prefers the texture and shape of these dishes.

He tends to communicate his hunger with his teeth.  He’ll either bite at my clothes if I’m holding him, or he’ll start trying to rip up the rug if he’s been out to play as is often the case.  He’s only bit on fingers once or twice and never enough to draw blood – just his way of reminding us that he’d like more of the lettuce those fingers were holding before he snarfed it down.  He’s picky about his carrots – so far he’s only liked them hidden in treat-form or in peels mixed in with his greens.  I put out a metal 9×9 baking pan with some of the aspen litter I’ve been using and he and I have adjusted it’s placement on the rug until he is mostly litter-trained even when he is out playing in the family room.  The real problem is the litter itself.  I’m thinking I may need to get some sort of rug that will keep the litter in as he leaves, since it’s ending up all over the rug and then the kids’ socks and beyond.  Ugh.  I keep sweeping up and then snagging the dustbuster to deal with the stragglers, but I’ll have to work on a solution to keep them from getting so far.  I’m thinking we could get a rug to extend off the carpet, but I’d need something that will either attract and keep the litter or have an edge that sticks up?  Perhaps my bunny-savvy friends will give me some ideas there…

There are more pictures, some with Kayla too, and hopefully I’ll get some others online.  Meanwhile, I’m overwhelmed with the backlog of things that didn’t get done before or during the holiday break and also usually feeling overmedicated to the point of either exhaustion or tears or both, mixed with a healthy dose of the usual pain.  Ugh.  And now, somehow, the husband and one of my friends who are both tracking workouts and calories on an iPhone app have gotten ME tracking the same info for myself.  It’s only been a couple of days but one of them I nearly doubled the amount of calories the damned thing allotted me.  It was at least a little heartening yesterday, when I snacked, had all three meals AND dessert, but came in nearly 300 calories UNDER my target… because I’d worked out that morning.  Heh.  If only I had the time (and energy) to do that every day.  I hate diets.  So I’m NOT dieting.  I’m just… submitting to peer pressure.  *sigh*  I’m going to miss aobut 1/4 of my own cooking, as  Brian slowly goes through my recipes as I cook them and determines the calorie intake per serving.   While most of my recipes ARE turning out just fine, SOME of them are just decadent.  Although, even Brian says that the app calculated a smaller calorie budget than he would have suggested, so I have a little wiggle room.

On the medical front, I’m going to be getting a second opinion in a couple of weeks, from a different doctor.  It’s not that I don’t believe I have this Fibromyalgia thing.  It’s that I want the “healing” process to involve less drugs and yet happen SOONER.  I woke up around 4 am a week or so ago and found myself staggering and stumbling drunkenly when I tried to get to the bathroom.  I FELT drugged and it was frightening.  I’ve been feeling a lot more shifts as time-release drugs kick on and a lot more moodiness from the most recent drug addition – Lyrica.  I’m seeing the Rheumatologist tomorrow though, and I’m sure she’ll either dial that one down or change it.  Nonetheless, I’m still going to go for the second opinion.  I’m growing more concerned that my high blood pressure is on the sidelines and I’m just on too many meds as it is to add another one so I’ve been stalling both my primary and my cardiologist from giving me anything.  I need to have OTHER stuff removed without leaving me in agony – and I’m already in some pain as it is, since I’ve been refusing to up the dosages on the pain meds.  I don’t need to be any more drugged up – I have enough days that I feel like I’m wading through a reality fog just to focus on the task at hand.  And some days I have to bully up my willpower just to go from sitting to standing as I never know if I’ll find more pain in the process.  The idea was supposed to be that we were going to retrain my brain and body to understand signals correctly, but I’m still getting the same signals – some seem to be getting worse!  There are days I just want to stay in bed.  My emotions are all out of wack, so I sometimes burst into tears over the tiniest thing…

Oof.  Enough of that.  I could go on for hours.  But I’ve got a little boy to go get from school, a little girl to wake from her nap, and a bunny to play with when we all get back home.  I like those options MUCH better.  *grin*

Perhaps I’m not TOTALLY a cynic after all…

But Baby, It’s Cold Outside…

Not long ago, a lady looked at Kayla and I in the hardware store and asked me “How can you refuse that cute little girl anything?“  and I had to reply that sometimes… I can’t.  This bright-eyed little face decided to come inside from playing in the snow.  I popped off her hat and found curls and a smile waiting for me.  I took pictures and then we ate the snow off her scarf.  Heehee.  I suggested it tasted like “cold Outside” and she sagely agreed.

The Longest Night (part 2)

11:36 pm.  Solstice Night.  The children tried their best to stay up ALL night.  Frankly, I was impressed they made it past 11:00…

click to view larger

click to view larger

Now it’s all up to the grownups to keep vigil, awaiting the sun’s return.  :-)

The Longest Night…

Tonight is Solstice, the longest night of the year.  For those who don’t know, this is what we celebrate in our little family.  A few years back we startled everyone when we suddenly announced that there would be no more gift exchanges from us.  While we do enjoy and continue to attend ALL the family gatherings, as they celebrate Christmas – we celebrate Family and the spirit we hold within our own home-made holiday.

There are plenty of people who already celebrate Solstice (mostly Wiccan, I believe), but we didn’t really consult them when we fashioned what WE wanted our holiday to be.  “Fine, let’s just celebrate the seasons,” I had told Brian one night after we’d had the same old conversation about how Christmas didn’t “mean” anything to us anymore.  Since Brian studies things like Shamanism, he couldn’t argue the logic of celebrating the four seasons instead of Christ’s birthday or the Hallmark/Santa gift holiday.  Christmas had become an exhausting ordeal of gathering the “right” gifts for everyone and worrying that it wasn’t the right one after all once it had been wrapped.  I’ve always enjoyed the cooking aspect – especially when they let me delve into the wonderful world of baked cookies and chocolate delicacies.  I’m already waiting and thinking on what I intend to bring this year.  We kept that tradition, oh yes.  But, since we weren’t practicing Christians, it seemed hypocritical to be celebrating the birthday aspect.  So Brian suggested we celebrate Solstice & Equinox holidays.  And, since then, each year we work to slightly define each holiday just a little bit more.

Winter Solstice is the longest night of the year and, in ancient times, they feared that the sun was leaving or burning out.  So they would light fires and keep vigil, praying for the sun’s return.  In respect to that heritage we will spend tonight staying up and keeping vigil until the sun’s return in the morning.  At that point we will feast and celebrate (before passing out in staggered naps, I expect), making seed and peanut butter pinecones for the birds and maybe even stringing popcorn to hang on the trees.  Some of our family members will be joining us (most have to work this year) for the breakfast feast and we’ve scheduled it so that the feast will begin shortly after the sunrise so that we can all see it together.  We, at least, do not take that big ball of light for granted.  Let us celebrate it’s continued nourishment, as our world would not be habitable without it.

As for the long night itself, the kids are excited that we have told them they can stay up.  I imagine they’ll make it a couple hours past bedtime at least, although I suspect that Jareth will try to make it further before passing out on the couch or something.  Once they are asleep I’ll wrap up the little things we’ve got for the stockings.  Nothing, however, ends up wrapped beneath the Solstice tree (yep, still have a tree too – not so different from all the other households, really), but there is a little bit of gift exchange mostly just some fun little stocking stuff and this year’s gift – one blue-eyed, white dwarf rabbit named Snowflake.  Last year we got fish (not nearly warm-fuzzy enough for my needs, but fun to watch) and the children each got a wooden toybox which we spent part of the next day painting with them.  This year we’ve got other craft plans – peanut-butter birdseed balls, made with pinecones we collected in the fall.  We might also do some popcorn strings as we never got to that one last year.  We also are going to make our own ornaments this year, since I’ve come up with a craft that even Kayla can do – felting!  I picked up a felt kit during a holiday market at our school.  One of the parents makes them (http://www.mysmallwonders.etsy.com) and she had a cute setup with a felting needle, unspun wool, a foam block, a cookie cutter and some instructions.  I tried the kit, which was one to make a flower, and enjoyed it quite a bit.  This resulted in my sending off some felted flowers in with the cards my kids drew for their teachers this year.  I was hedging on doing it (since I’m pretty sure ALL the teacher have felting experience at that school and my efforts are probably amateurish at best), but Jareth liked the idea and made me do it.  What can I say, I let them twist my arm when it comes to the non-essentials.  I just hope the teachers liked them.  Next year, I’ll make the kids do their own, after they’ve had some further practice, starting with the ornaments for this year’s tree.

Other plans on the agenda tonight include talking about how last year went - compared to how we wanted it to – and how we envision the next year.  This is the time we really decide on those New Year’s resolutions, really.  Time to reflect and dream.  Time to visualize how to make those dreams a reality, or at least get a step further by next year’s end.  We also take time during the long night to gather clothes from our closets – things we no longer wear – and pile them into bags for donation.  Our way of trying to give back to the community around us.  As the kids grow older, we will find other activities to include for community as well.  We’re considering going through the toys this year too, as there are a lot that the children have either outgrown or no longer play with.

We often get ambitious, and there will be some things that don’t get done tonight or tomorrow, but then I don’t expect that to be any different this year.  After all, we have a bunny to play with!  I’ve already spent half the day just lounging about in the family room, letting the rabbit run free.  Brian got a bunch of Plexiglas and installed it into strategic points to prevent the rabbit from getting into a few restricted areas.  So, except for when I needed to run my back-saver (roomba) around the family room to clean up some hay from last night’s play, Snowflake has been exploring the family room (and the kids) most of the day.  I am amazed at how easily this rabbit is handling the bouncing and hopping of my two loud rabbit wannabes as they spent most of that time bouncing on their knees, trying to encourage Snowflake to jump around like them.  I will admit, there were a few moments where I think the bunny was outsmarting the kids…

Happy Solstice everyone!  Sleep soundly, for we will be keeping this night’s vigil.