Seizure

 

 

I hope you get a chance to relax and enjoy this little video I shot and put together for you. Meditate on the things that matter to you, as I also do.

You see last week I had a nasty seizure which threw me back on my progress chart a few degrees, both physically and emotionally. It’s not easy to climb over thoughts such as “not again”, “will I ever”, “I just want to be” etc but giving up its not an option for me since I have too much to lose and would hurt too many people that I love. So I must go on. But getting back up, and moving forward while hurting, having half of my body not functioning as it should and wondering how long will it take until I fully recover is not as easy as you may think. I wish I could be poetic about all this but pain and struggle bring more misery than poetry (unless its some sort of emotional heartbreak and then you should see my muse dance and come up with all sorts of rimes and wisdom:) But for now I try not to fall on my face as I experience dizziness, I try not to walk into walls as my balance seems to be taking a vacation, and I try to smile through the pain all my limbs seemed to join in. I am weak and strong, frail and tough, happy and sad.

What caused such a relapse? Accumulation of stress (I like to collect:) Nasty flue which left a frail immune system exposed, taking up nursing duties as my family laid ill in their beds, work, and the happy visit of my cuz. But the body can’t recognize happy stress from bad stress, just files all that info in the “STRESS” file of my life while smiling knowing what’s to come. But I drove downtown! Took my cuz and my daughter to the Seattle Space Needle and other places and I’m sure inside my head there was a small voice protesting to all the exitement…which I clearly ignored. Did I learn my lesson? Depends on which side of the lesson you are. I would say, yes, then explain. I’ve learned that I have the strength to drive downtown (even if for a day every few months:) I’ve learned that my body is getting strong and able to handle more fun, I learned that relapses do happen and not to focus on them, I learned I’m fun again! Even if in a small increment at the time:) Did I learn my lesson? You be the judge, but I no matter what you decide I smile the whole way because I DROVE DOWNTOWN SEATTLE AND HAD FUN WITH MY CUZ AND DAUGHTER ON TOP OF THE SPACE NEEDLE, and that to me is priceless and worth every muscle twitch and pain;) I would do it all over again the same way, no regrets. Now go have a good time living life in whichever increments of strength you can muster, and when herxing (for my Lyme warriors or all with any autoimmune troubles:) smile because you got to the herxing reaction by living life and in the end you had a say, a choice, not the stupid illness that’s trying to kill us:)

God Bless:)

My gratitude towards you explained.

I asked myself today: why the urge, lately, to write about people that made a positive impact in my life?

It’s not a sudden urge. I’ve had these emotions accompanied by fond memories deep within myself for a very long time but I never acted on them. It seems the deeper I care about a person the harder it is for me to express it. Is it a flaw? A weakness? An oddity? Or am I simply a normal human being. Upon reflection, I’ve gathered that is far easier for us humans to express anger, displeasure, and critic of others to their face (even easier behind their backs) than give them an honest compliment. And if any measure of a compliment holds an element of insincerity it shatters something within us, it shatters our trust, and without trust, a real friendship can’t exist.

Only when I became ill, and I myself received encouragements did I realize how valuable spoken support really is to a human mind, soul and spirit and I thought to myself: I may die soon and they’ll never know how much they mean to me! Unless I tell them.

So what was once buried deep within my heart is slowly but surely making its way to the surface. This may be a cheese way to express such gratitude and at times love, but what can I say? Progress and change enter the world one step at the time. The important aspect is that arrives sooner rather than later, right? So, don’t lose heart if your name hasn’t popped up on my blog just yet, it’s coming:)

God Bless:)

It’s been a while since we talked

D516A709-B2B0-4A0F-8052-D12A5AB364E9What a great summer this one was for us:) The apartment construction work is almost done. I had the most wonderful and unexpected visit for Easter from two of my brothers: Sergiu came from Germany and Flesh came from Romania. IMG_0666They took me completely by surprise:) We had a great time showing them Seattle, among other things and after they left and the weather warmed up, Chet and I spent many hours cycling on bike trails with my in-laws:) IMG_8327I also took lots of macro photos, a hobby of mine, and you can see one such photos at the very top (honey bee on a clover:)

I’m getting stronger every day. I have changed my Lyme tincture treatment to a new product and so far I think it helped me the most (or I’ve had lots of help from previous treatments and this one sort of sealed it). It’s a new product I found on Amazon called Holistic Tincture 7, made in Germany. It’s a 13 Herb tincture (Japanese Knotwood herbage, Teasel root, Cats Claw flower, Coriander herbage, Garlic, Hawthorn leave, Sarsaparilla root, Devil’s Claw root, Boneset leave, Astragalus root, Olive Leaves, Panax Ginseng root, Ginkgo leave) specifically design for those suffering from Lyme. Currently unavailable on Amazon as of today, but you can go directly on their website at http://www.biotraxx.eu to order. Heads up their info is in german (Amazon has an English version), and you need to take 20 drops three times a day for 6 months. One bottle lasts about 2.5 weeks. IMG_0265.jpeg

It really helped me so I hope it does the same for you:) (The cost is around $28 per bottle plus shipping $7).

This year we’ve celebrated our 26th Wedding anniversary:)B26CB92F-1A70-4DC3-9F93-62BD8A5CC31E

I’m grateful and I’m looking forward to the wonderful things to come in this life:) So keep on fighting for those ones not yet on the other side because there’s hope:)

Here are a few more pictures I like sharing with you:)

Have a blessed day and talk to you soon:)

Living Proof-MS Hope

http://www.mshope.com/

https://www.seelivingproof.com/

https://www.imdb.com/title/tt6604174/

I’ve watched this documentary a couple of days ago while in sickation (sick vacation) on MS, knowing people who struggle with this disease, and I strongly recommended to all MS patients out in the world.

About a month ago, unbeknownst to me I began eating a vegan product (fake bacon) and loving it. I would make sandwiches with it and top it with pepperoncini, lettuce, cucumbers, and vegan cheese and smile all the way to the last bite. Then I began feeling some of the old symptoms creeping up, symptoms such as severe fatigue, foggy memory, walking into things, nausea, fever, dropping things all the time, to name a few. Relapse or Lyme-flare was my diagnosis and began treatment right away. It would work until it wouldn’t. I upped the dose and went around the same circle. I would get better only to get worse. What in the world was happening? My joints hurt so bad, especially my hips, I was having a very hard time walking. Meanwhile, I was happily eating my vegan bacon sandwiches. About one week ago, as I was getting ready to make yet another sandwich Chet read the ingredients, for his own reasons, and exclaimed.

“Carmen, did you know this bacon has gluten? Sugar, water and gluten in concentrated form?” My brain was too foggy to process the info I was just receiving and it took me a good while before the truth absorbed between the smoky creases of my brain and into the information center where it could be processed before a response was delivered.

“What?”

“You’ve been on a gluten feast for a month!” He exclaimed in response as we both began laughing. Such privilege yet no recognition.

Well, my vegan sandwich days came to an abrupt halt. It will take a good while until this intake of gluten will be out of my system, meanwhile, I learned a few more lessons.

  1. I’ll stick to real bacon and leave the vegan diet for Chet (who’s been a vegan for the past two years now).
  2. This gluten intolerance issue is not in my head, it’s not a mental/emotional issue I came up with and just need to snap out of it, it’s real and there’s a reason why. This second point goes along with some of the information in the Living Proof MS hope documentary done by Matt Embry who was diagnosed with MS about twenty years back and fights it different ways but mostly through diet, exercise and supplements like Vit. D. Diet is the evil of most diseases and the medicine for all cures.
  3. Read and inform yourself well, without assuming, like I did, that a vegan product automatically means a gluten-free product.
  4. I balanced back quite fast once I stopped the gluten, which tells me my body and mind are serious about getting better:)))) But, I got the flue, along with every single member of my family except Alex. They’ve been in bed for a whole week before showing any signs of life. Today is Chet’s first day back to work after an entire week spent on a horizontal sickation.
  5. Grateful. There’s always a solution for every problem, just read the fine print:)
  6. P.S The words look a little funny to me so any grammatical or expressive mistakes are due to my gluten feast. God Bless:)

ME/CFS or Conversion Disorder speech on Ted Talk

ME or Myalgic Encephalopathy, also known as CFS or Chronic Fatigue Syndrome or Conversion Disorder. 

It’s surprising how about 99% of her symptoms I dealt with and some which remain still deal with. The good news is that I feel soooo much better, despite the mild relapse the past month where I couldn’t touch my chin to my chest due to stiffness and intense pain in the back of my neck and fatigue unusually higher than usual. I’m back on Lyme 2 a tincture that helps calm down the symptoms. I still have a very stiff back neck that crunches all the time I touch but I am so grateful for life in general that I move along:) I have a part-time job now; two hours two times a week cleaning a house, and I’m so happy and proud of myself to be a working woman again. I have deep anxiety before I have to leave, but I take Neurocalm which helps me and this week I’ve just begun drinking Sarsaparilla organic tea which gives me quite a bit of energy and calms my central nervous system as well. Amazon has a brand I use called Buddha Teas, but there are other brands out there to choose from.

For all fellow Lyme Disease, ME, CFS, Conversion Disorder, Cancer and other Autoimmune Issues too many to name, I honestly pray for your complete health or at least bearable symptoms. The cure is out there, we haven’t found it yet. Meanwhile, keep fighting, keep researching and do whatever it takes to heal yourself because if we are to wait for western medicine to do it for us we’d all be dead by now. Maybe one day they’ll catch up as well because they’re seriously behind in autoimmune disease knowledge.

Merry Christmas to everyone reading this blog and a Happy New Year full of an unexpected improvement in your lives.

God Bless:)

The Spandex Curse

Sunday morning, needing to breathe some fresh air, I stopped at a tiny coffee shop here in Magnolia where they make my favorite decaf latte with almond milk drink.

The coffee shop, located in a deserted looking minuscule strip mall, has a male barista and a barbershop feel. Beside the male barista, a man in his 40s or 50s, two other gentlemen were occupying the small space, one on a stool to my left and another paying for his order.  All three laughing. The laughter and under the breath later on giggles were coming and going like a tidal wave and I smiled, happy to see them having a good time. I ordered my coffee, paid and waited. Picking his own coffee the man by the registered left for few seconds then returned, taking a seat on a stool next to the other, all three still giggling. One of them kindly let me in on the humorous secret.

“He just got caught staring at a guy in spandex.” Another wave of laughter.

“You wonder sometimes if people look in the mirror before they leave their house and think: sure, I look alright!” The other one, who got caught staring, now facing the wall, head bowed low and away from me, as if ashamed by his misfortune, spoke.

‘He’s still recovering.” The first man clarified to me, while everyone else kept laughing, me among them. The victim turned around and continued.

“And he was not in good shape…more laughter…I mean he was fat…in spandex.” The poor guy still looked terrified but what he’d witnessed that day and we joined him in laughter.

“I’ve had few such recoveries myself,” I replied, now holding my coffee.

“Have a good day.” I wished them still giggling and left them behind to their recovery ward and medicine. I love the way men talk. Simple, to the point and always with a touch of humor.

Have a great day:)

God Bless:)

Homelessness of the heart

The heart, fatigued and aging, is always on a journey. She starts full of such light but her innocence has been beaten out by shrewd beasts pretending to be her friends. Promises were made to her only to be broken, and the pattern repeated enough times that she hardened and no longer ventures out to the pastures. For a time sheer anger filled her every corner, as a result, she only lashed out. At other times she received kindness and a soft caress and she melted within and without. She loved back and gave herself gladly for it was worth it, but despite the good life and love, she knew someone was missing. Most everyone else called it something, but to her, it was someone. This, someone, was hard to understand or see, its presence was only felt when she took the time, but most days she was busy giving. She often finds herself homeless, even if for a short period of time, or longer. It’s the rejection that builds the lines of sadness and its the acceptance that builds the wrinkles of life, but despite it all, this someone is who she really longs for, a presence beyond her wisdom and time, someone she heard of from so many voices but there’s still a verdict out for what she really thinks of this someone, yet, it’s the someone she longs for because only that someone understands her potential. At times, the heart rests, fully content within her existence, she wants nothing, she needs nothing, she just is. And that someone is always close by in such moments, so she rests and listens. Maybe today she’ll finally meet someone. If not, she’s still happy, even if tired. -Carmen McKnight

The bubble, or the marshmallow as Chet calls it, is getting to us all. The claustrophobia, the lack of fresh air and the stuffiness are not elements a human being was created to thrive in. This environment is digging out of me an issue still unresolved.

This struggle has been unbeknown to me until earlier this year when my heart divulged, as a result of prayers and contemplation, what’s been hidden very deep within the layers of the soal and once exposed the tear glands shed years of struggled emotions. I’ve felt homeless within my own home and heart for many years. As a result, I’ve operated out of an orphaned spirit for years. While young, I had the strength to pretend otherwise. Age brings a whole lot out of the canister.

Let me explain.

I was told, while young and growing, that the home in which I lived was not mine and I could be kicked out anytime I stepped out of line. Now please remember this, I have forgiven my father, there are some old wounds that still need healing but all in all a lot has been healed already and life is good.

When a child grows up with the notion that there is no place in this world for them a complex called the orphan’s heart sets in and with time builds strong roots. When a heart does not have a home, as I suspect most people feel that, it always stays busy searching. That’s actually good.  Searching means moving and movement is life and life-giving and one day the answer or part of the answer will reach those who search. It was the man, in its weakness that hurt us and it’s man in its strength that helps us heal. God built both of these men from the ground up, man chose, consequences followed. So what was once torn down it can be built up twice as strong.

Thanksgiving is a holiday celebrated in the heart of a home, as it should be. But some may feel like you’re intruding like you’re a foreigner like you don’t belong. But we always belong, maybe not in that home, but there is always a home for everyone.

As I’m walking my road towards growth I keep on asking myself which wolf will it win? Lie or Truth? The answer is The one I feed.  

There is nothing weird about a struggle, it simply means we’re all human beings and the growth process within has not ended yet.

Gob Bless:)

 

P.S When happy, I don’t feel the need to write blogs. It’s as if those moments of happiness are so personal writing about them would only taint and diminish their value. But hardships and trials trigger my creative juices so much that I begin a downloading process of imaginative and heartfelt moments who, by some odd impulse, I need to share. I’m sharing this with you when I’d rather keep it private. Weird.

 

 

 

Our world and its influence on us

As you can see from the pictures below, we’re living in a bubble during the following renovations months.IMG_3392IMG_3485-1E2F020C0-7348-405B-BDA7-3606DA812B47

Due to asbestos and lead findings in the windows seals, the whole building, along with all the windows, has been fully wrapped in a protective white plastic sheet. At least it’s not black:) Even though it’s suffocating and unpleasant at least is a temporary inconvenience. In comparison to other people’s lives who have been ripped apart by all sorts of tragedies, this inconvenience is minuscule. So I’m greatful.

I find myself outdoors taking daily walks and on such walks, sometimes, I bond with neighbors. This morning I was talking to a retired female who used to work for the Post Office and lived in Seattle, where she was also born, most of her life. There were a few years back in the old days spent in Canada when she used to be married to her first husband, who happened to be a Canadian. She liked living there, mostly but found herself frustrated over a few of the socialistic perks, specifically health care. While talking about this and that she turned the conversation towards the politics. I understood the temptation since we just had mid-term elections on the 6th of November. I could swear that suddenly I was talking to my in-laws. She used the same terminologies and verbiage, the same quotes and so on. The thing is, my in-laws and this woman never met, to my knowledge, yet her words were eerily similar if not verbatim to those of my-in-laws when it came to her political point of view. I walked away knowing such verbiage was learned from TV news reports or newspaper articles, which reminded me how powerful the media is in shaping people’s minds. And that gives me a lot to ponder on regarding my personal thoughts and beliefs which I constantly evaluate and re-evaluate and change when needed because inevitably our world has an influence on us.

On a personal note, I have a part-time job now and it feels fantastic to get back into the swing of things. I’ve joined a book club as well and being part of the community around me is good not only for the soul but for the body as well. Small steps, giant accomplishments:)

Chet’s B-day, yesterday, was a happy event celebrated in the intimacy of our family:) Next week we’ll be celebrating my beautiful girl Meleah’s B-day:) I can’t believe she’s turning twenty-two years old. Time sure flies when you’re having fun, or even when you’re not having fun:)))

Merrill moved in about three months ago and we’re complete again, even if a little cozy in the small apartment. I would much rather have it this way.

Happy with our lives, thankful to God for health, peace, and love. I hope you’re doing well. (For the Lyme sufferers or all other autoimmune disease sufferers, keep on fighting because there is light at the end of the dark and most days unbearably painful season you find yourself in now. Psalm 23 rescued me.)

God bless:)

IMG_3512

 

 

Before the wind touches the soul

I’ve picked up a new habit, electric skateboarding…sitting style:)

I’ve never skateboarded in my life, however, that recently has changed after trying out Chet’s electric skateboard. Then I’ve ordered mine:)

Usually, I experience fear before getting on the board and if I did let my mind run wild I could easily talk myself out of a potential fun time. The imaginary bad scenarios can be scary:) So I stop the doubt. I have to find my spot on the board just so, one mm off and I get the wobbles and have a hard time turning. I feel the board for a few seconds making sure we’re in agreement. Then I start and as it slightly jerks me forward my stomach tightness and fear wants to have the final word.

These seconds or minutes before every single ride are the hardest; the body works hard in convincing me that laying comfortably on a couch and away from any potential harm is a better idea. But before the wind touches the soul it must touch my face first and for that to happen I must ride. So I do and few seconds in I feel a deep sense of freedom and joy hard to explain. I feel light and no longer burdened. I simply savor the moment of pure bliss.

In life many times we find ourselves in similar situations. The fears of what ifs can intimidate us into complacency and away from joyful moments. It can keep us in the fear zone (which in reality is infinitely smaller than the fun we can have afterward) and prevent us from building another beautiful memory worth preserving.

Pass through the fears of the moment so you can let the wind of joy touch your soul.

The video shows my mother-in-law, Janet, on her electric bike and me on the electric skateboard. Chet’s videotaping:)

P.S. I am impressed by my mother-in-law who battled and won against cancer, and to see her out and about living life is wonderful:)

God Bless:)

http://www.wowgoboard.com

Loneliness during illness

I began this web/blog site with the intent to keep a track on my medical info, since my short-term memory was seriously injured- still is to a certain degree, which can be a fantastic blessing when I get frustrated over small things, because I soon forget them and I’m left without a reason to stay mad:). Another reason was to encourage, if possible, anyone out there in the same situation as mine.

I had a great job and relationships before the illness, my life was on a high peak of happiness and contentment and I worked hard to get there. That changed literally overnight. But something that took me by surprise was the loneliness that trickled in along with the illness, like two best friends, inseparable and intent on causing trouble. I was cast aside, no longer a productive and effective member of the society. I call it “the silent depression” and I now understand how horribly it afflicts the ill, especially the chronically ill, and the senior citizens. With Lyme, as with other toxic and neurological illnesses, the mental clarity and health deteriorates and one’s personality changes. I used to feed off the energy of multitudes of people and found solitude boring and useless. Not now.

So I sat down this morning having my breakfast of tea and a gluten-free/vegan carrot/banana bread (not my usual breakfast, but I baked last night:) thinking of all the other ill people out there in the world and the loneliness they may be experiencing. What can I say to be of encouragement? What encouragement can I receive for myself?

For those who believe in God remember that He used the most imperfect people, men and women, to do great things through. It’s never too late, you’re never too weak, to ill or too fragile to be a strong force for those around you. I am like Issac who was a dreamer, but God ended up doing great things through. What about you?

Rom. 12:15; 1 Pet. 4:10; Ex. 14:14-The Lord shall fight for you, and you shall hold your peace:) These are some verses to encourage you:)

For everyone:

Forgive.

Meditate on good things (health and a cure and remember not everything has been discovered. I strongly believe there is a cure for Lyme, Chronic Lyme, Neuro Lyme etc, even if it has not been discovered yet, but above that I believe that our body has the ability to heal from anything if given the proper balance of nutrients and extracting all toxicity out of it).

Help others. (That means even if you can only pray for them, or smile at them, or give one word of encouragement, it gives you a temporary break away from your troubles).

Make a plan for what you want to do when feeling better and start planning towards that. Here you’ll have to be realistic and change some of the past goals and plans.

The internet is a source to reach out, through support groups, but be careful not to get stuck in the negative cycle of complaining only. Some days you’ll need to unload, and you should do so keeping in mind that your audience is hurt too, but than don’t forget to smile and laugh. (Watch comedies).

The best cure for loneliness is health and being part of the society once again, until then fight like hell to get there, and I promise you once you make it to the other side a wiser person will emerge on the other side.

I’m reading this book now, and I love it. It’s a look into the human body/autoimmune/cell function with a biblical insight as well. For those who don’t have a passion for the medical field, this may be a bit boring, but it’s not hard to understand. Well written and an easy read.

http://www.scriptum.ro/librarie/mai-presus-de-stiinta.html

For those who want the book in Romanian.

God Bless:)