Just Breathe

D1_LIP_TIE

We might take for granted that we breathe.  It’s something we don’t think about often, until our passage ways, by which we take in oxygen, are blocked.  Either we’re stuffed up, or swollen up, or something toxic in the air prevents us from breathing…

How much thought have you given to breathing while you sleep?

Do you snore?

Are you a mouth breather?

Do you “smack” when you eat?

Messy eater?

Drooler?

Have trouble swallowing?

I remember my snoring and lack of ability to breathe being SO bad during pregnancy, my husband asked the doctor if I could “die” – because it sounded like I was gasping for air.  Yes – it was really horrible.

We had our first official “meeting” via Skype with our Oral-facial Therapist this week.  The woman who has insight into helping my 14-year-old be able to close his mouth, retrain his tongue, and avoid yet another round of braces.  Time is of the essence.

Something I didn’t realize until a few days ago, D1 has a lip tie, in addition to his tongue tie.  That’s partly why he can’t close his mouth.  His top lip is “tied” to the skin of his face inside his mouth, not allowing him to pull that lip OVER his teeth, and close his mouth.

His lips are always cracking and dry.  He is a horrible mouth breather.  It often leads to bad breath.

All of that seems pretty minor, comparatively to the quality of sleep he has been missing over the years.

Sleep is essential to your body healing.  Its’ when you repair and recover…. and grow.  There is growth hormone only created when you sleep.

So while getting your inflammation down, and eating a real food diet is helpful, as is increasing your zinc, and getting enough vitamin D…

If you’re not getting the proper oxygen throughout the day, and you’re not getting the oxygen flow at night.

Guess what?

Not cool.

So we discussed all of that… and next week we’re setting up an appointment with an ENT to take a look at D1, so we can address these issues with him first.  I’m fairly positive he isn’t the only one who will be addressed – but the palate expander on several of the other children HAS helped address things dramatically.  She said when you’re talking about even tiny millimeters of space “cleared” to allow oxygen flow, you’re talking huge differences.

While we talked, she shared part of her story.  Very similar on some levels to mine.  Metal toxicity, and healing her body inside out.  She encouraged me to look into expanders myself.  I told her my orthodontist seemed to shy away from that, at my age…  she disagreed, and said it was the best thing she has done, although they used removable devices, so you can eat – it has made HUGE impacts on her sleep and healing.

I can imagine…. just how much that is impairing my healing process.  I do sleep – but I never feel rested.  I just don’t.

She explain how braces used to be addressed, vs. how they are now…  The teeth on top were “aligned” and the bottom jaw was “tucked” under.  (If you can visualize my profile… Beeker from the muppets comes to mind!)  She went on further to say that once you set that bottom foundation – then you set the top teeth on TOP of that, you have a set up a healthy breathing space needed to function.  It changes your face shape, but more importantly – you can breathe.

I try not to think about what if…

However…

What if someone mentioned that PUPPS was related to celiac disease.  I could have changed my diet, instead of being put on steroids… and the snowball that got me to now.  What if my son had been “clipped” years ago… and nursing hadn’t been such a struggle.  Would that have prevented post pardum depression, and all of the issues that were created from lack of family support during those very trying months?  What would be different now?

My head spins.  Literally.

I cry at how many times I didn’t “get” that my son said, “I can’t control my tongue”.  I mean, I get that it’s a strong muscle… but WHO can’t control it.  Seriously?

We have lots of months of things that were include many trips, most likely surgery for multiple kids, as well as myself, and then therapy for a long while to get these things corrected.  It’s not going to be a quick thing.  We’re going to have to make adjustments to not just throw ourselves into things that eat up our time.  We have to make a solid effort to heal, and be open to changes that need to be made.

Most people would probably cringe at the thought of all of this, but I’m actually VERY excited.  I know this is going to help us tremendously.  We are thankful to God, for the knowledge and advancements being made to understand our body better.  Never assume God doesn’t know what He’s doing.  The one thing I didn’t mention – just how much He has grown me, and strengthened our marriage through this process.  It’s solidified our relationship with our kids, and given them opportunities to trust in Him as well.

God is good.  ALL the time, He is good.

 

“And we know that all things work together for good to them that love God, to them who are the called according to His purpose.”

Romans 8:28

Posted on May 24, 2014, in Auto Immune Disease, Our Struggles and tagged , , , , , , , , , , . Bookmark the permalink. Leave a comment.

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