Showing posts with label mthfr. Show all posts
Showing posts with label mthfr. Show all posts

Thursday, January 28, 2016

Winter Detoxing and Stuff

But do you even dry brush? Detox bath? Drink lemon water? Sweat it out in a sauna?
Quick drop in. It's still cold, people are sick, joints hurt, skin is dry, here's some potential remedies. If anything pamper yourself. You owe it to YOU.
Who cares if it doesn't work. It feels AH-mazing. Dry brushing scratches my skin in a way that my nails won't and it makes it feel soft. So, here's how it's supposed to work. You get a brush. You start at the bottom of your body, at the feet and in circle/oval motions you move up the body towards the heart.


Benefits.
* Exfoliation of the dead skin cells. I could always use new and younger looking skin.
*Lymphatic circulation. Yes please. Get those toxins OUT.
*Clearer Pores. Again, what's not to like about this?
*Increased blood flow.......better circulation....heart health.....I ain't getting any younger. Another health benefit.
*Some claim cellulite reduction.
Try it. Do it. You're welcome.

Detox bath. Lymie or not. Everyone should get one of these in at LEAST twice a month. I do once a week. It consist of super duper hot water, epsom salts, baking soda, and an essential oil such as lavender. The epsom soothes the muscles and drawls out toxins, the baking soda softens the skin, the lavender because it is my favorite and if I could my master bath and master bedroom would reek of it at all times. So, whatever your favorite reek smell is, feel free to reek away.

Lemon water. It's good. It's a good way to get your water down for those that don't like to drink their daily intake. I'm still not sure if it's pseudo or not, but I'm pretty sure I can hear everything flush when I drink lemon water after I've sat in the sauna, came home and dried brushed and had a good soak in a detox bath followed by a nap.

Our bodies get a build up from the things we do to it, the stress we physically and mentally place on it. Illnesses and disease, busy schedules, the foods we put in our bodies, medications. Take time to give your body a break. The inside deserves it just as much as your nails, or a new haircut, or a foot rub. All these things are just as important. Diseased or not.  Be kind to yourself.
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Monday, July 27, 2015

Wouldn't It Be Nice

That is the song that will be stuck in my head today.  Weekend was excellent. Breakfast with the parents, farmer's market, kite festival, lunch with husband, yard work, and I got to hang this beauty:


We got our new porch back in May and I'm still painting it as energy and time allow. I love the bird watching, grilling, and reading I do out there. It is my little escape. The chandelier has been the perfect addition thus far. I even managed to start on my little succulent garden. She is kinda puny at the moment, but I look forward to seeing how she grows.

I have plans for this week. Going to try to get back to the gym, do some detoxing.
I have this mental exercise I do every morning when I wake up. Having "lyme brain" causes forgetfulness and confusion more than I am willing to admit. I may forget something that happened years ago or I may forget what I was talking about mid sentence. Almost always forget where I park. I've always been a chatter box, but I find myself more and more just sitting in silence. Afraid of what I may sound like to others, I just keep my trap closed. Friends and family understand. The general public doesn't. I can see it in their face. Like either I am too wrapped up in my self to care, or I'm the girl who is "really starting to lose it".

The morning drill for me consist of me opening my eyes, taking my thyroid pill, and laying there and making a run through: What day is it, year, address, my name, my husbands name, all of my children, their birthdays, important days. I try to run through recent events. How far back can I go with my dinner. What did I eat last night, and the night before, what about the night before that? Then I scavenge for a few memories. Sometimes it is a little foggy, but they all come to me. Except dinner. I do good if I can go back 2 nights. I usually do not get past 3. Some days I am on point. I'm quick with the drill and know it will be a day of clarity. Others it is a little slow. This morning was heartbreaking.

Husband was getting ready for work. I could hear him in the bathroom. I rolled over to take my pill with my water. I rubbed my eyes, and moved enough to listen to all my joints pop and creak, Then I started. Today is Monday. Tyler Scott, Macy Elizabeth, Kenneth Ray, Amber Lynn, Elyse Nicole.
Birthdays are as follows. We made pizza on the grill last night and watched Netflix. The night before I didn't eat dinner. My husband is Kenneth Ray. We have been married for 6 years. WHO IS HE???? I know who he is. He is my husband. He isn't a stranger, but who is he?????? Where are our memories??? Does he love me? Who is he??????

NO! This isn't happening. Quick, my parents. Sandra and Gary. My brother and all his family........Got it. What the HELL is happening????

He is coming out of the bathroom. Close your eyes, Adrienne. Stop crying. He is going to come tell you goodbye and he doesn't need to think anything is wrong. Stop CRYING!!!

He knew though. He ran through memories with me, asking me if I remember our cruises. (I remember them, but I can't REMEMBER them). He asked if I remembered his marriage proposal and where we ate afterwards. Yes! He asked if I remembered how much he loves me. No. I don't know him enough right now to know how he feels, his likes and dislikes. I'm so confused. This sucks. He compared us to the movie 50 First Dates. I remember that. Made me laugh. Told me that if he has to remind me every morning he will.


Now, I have the scene stuck in my head where he plays the video for her each and every morning to the Beach Boys song Wouldn't It Be Nice.  At least something is sticking right?

OH POOP! I have eggs boiling. I'll be right back.

I obviously have mashed potatoes for brains right now. I'm sad. This isn't fun. I figured I had better blog quick before I forget. Like forgetful Lucy.  This has to be equally upsetting for him.  Lyme isnt fair. Not to the person infected or the family coping. I try to find humor in everything. I wish I had something more uplifting to share in closing. I apologize. Time for a neurologist visit and another MRI I suppose. One thing I do know is how much I love my husband. How blessed am I to have a man that is willing to take the time to be late so that he can talk me through our past? Blessed indeed.


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Wednesday, June 10, 2015

Kristen Wiig Reenacts My Lyme Seizures

It's 4AM and 2 weeks later. I honestly didn't think I'd be back this soon. Insomnia hit me a few hours ago, husband is off to a side job, and the cats are in the next room playing parkour again. May as well share what brain activity I can with you while I can right now. I do my most lucid thinking in the wee hours as it seems.  So without further ado, I bring you my next entry.

They are back. There has been 3 now in the past week. Well, 3 notable. When you hear seizure you probably think I'm spitting pea soup and wonder why I'm not in the hospital and how come my licences hasn't been taken from me yet. You are thinking gran mal. Usually associated with Epilepsy. That is all I used to think of as well. I was pretty afraid when I first started getting these disruptions in my body. It was pretty frighting. I've mentioned before I can feel mine coming. I get a sense. Sometimes I just go blank, or I will have an aura headache, blinding brightness in my eyes or extreme vertigo. Sometimes all of my senses are super-powered right before it will happen. I will retreat to my room. Here lately, it is just happening. Not much of a warning. In the middle of the day, in the middle of sleep. I loose my ability to speak, to walk, to control my hands, swallow, breath. The difference between the type of seizure you may think of and the type I suffer from.....I am wide awake during the entire thing.

 A seizure is defined as uncontrolled electrical activity in the brain, which may produce a physical convulsion, minor physical signs, thought disturbances, or a combination of symptoms.

To help you better understand, I will explain the different types.While this is scary as all "le chiz" to my family who has witnessed these episodes, I have to bring a #funnynotfunny factor to the table. I also have to find a creative way to keep your attention. For this reason, Kristen Wiig is gonna help me out.


******{this is not intended to offend or discredited anyone's pain and suffering as myself am a pain and suffer just tryin to find my way and that is my disclaimer}

There are 2 categories for seizures. General (produced by the entire brain) & Partial (self-explanatory)
Under General there are 6 different types:

*Gran Mal~ This is the most serious and scary of them all. The one you are probably most familiar with. The patient becomes tonic and loses all consciousness for 30-60 seconds and violently jerks before possibly falling into a deep sleep. Most commonly associated with Epilepsy.  I have never experienced this. Thank you, Jesus!

*Absence~ cause a short loss of consciousness. This only last for a few seconds. Patients are usually not even aware that this has happened. Only that there has been a sense of a loss of time. So THAT is where my day has been going!!!! For reals. I just blank out. I'm proof it is possible to think of nothing.


*Myoclonic~sporadic jerks. Usually on both sides of the body. Patients usually with throw objects if holding them. GUILTY. Ummmm......Kenneth, Remember that time that fork went flying across the room when all I was trying to do was put some food in meh mouth?

 *Clonic~repetitive, rhythmic jerks that involve both sides of the body. Been there, done that. Wake up the next day feeling like I worked out the night before I'm so sore. Friends, these leave me spent. These are what I have most commonly.


*Tonic~stiffining of the muscles. My kids got to witness this in my hand just this past weekend. The day after I had a Clonic. Not to be confused with a colonic.


*Atonic~sudden and general loss of muscle tone, usually limbs. Normally results in fall. The only time I have had a problem with this one has been when I have been doing some major herxing and I just lose all muscle control. I cannot even feed myself when I get to this state.



 Partial seizures are divided into simple and complex and secondary generalized. The difference between simple and complex is that with simple, patients maintain awareness whereas complex, they lose awareness.

This area affects the motor skills, the senses, memory, emotional disturbances. Jerking, spasms, and so on.
It is not uncommon for more than one of these to occur at a time. ANY of the above.

THYROID ULTRASOUND tomorrow. It has been 2 years since my partial. If I have a clean report, I'm G2G.  I visit a new doc next week and keep pressing forward. This solitude thing is a little more somber than what I figured it would be. I mean. I think the crickets can hear crickets. 2 weeks no social media now. I'm learning stuff. Life.

Well, this is all for now. I'm off to heal today. Kristen and myself thank you and wish you a sunny weekend.


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Monday, June 1, 2015

An Open Letter

Day one:

I don't often go back and reread my past posts. My mind is becoming more and more clouded these days, therefore I did this time. My emotional state has not changed much. My heart hurts now more than ever. Not a day goes by that tears do not meet my cheeks. I'm broken. I am defeated. I do not expect you to understand.

This past week my daughter had her high school end of the year choir show. An hour before we were to leave I was downing water and laying back after a bath in hopes of easing my tremors and the brain rattles I was having. I'm walking in a constant nightmare right now. I stepped out into public. This was a first for me. I have always hidden away when these episodes hit. They are just running into each other anymore. Too much for me to stay locked away. This was not an easy thing to do. The people, The sounds. The overload. I had to sit very still holding my arms as tight as I could at one point or I would have started having some major twitches. My husband wiped the tears from my face as I pinned my limbs and let my hair fall hiding my face from my parents sitting on the other side of me.

We left early out the side door before it was over to avoid everyone.

This is it guys. Friends, foes, family, strangers.....whoever you are reading this. I am not well. I am tired. Tired of the show, Tired of repeating myself. Tired of the pain. Tired of trying to please everyone. Tired of the madness. Tired of the bad news. Tired of being taken for granted. Tired of caring about some of you too much. Tired of smiling.

It hurts to walk, it hurts to turn over in bed, it hurts to breath. This is mentally taxing.

 I      am      depleted.

..........hold on.....I was just asked to come help and climb a ladder.......case and point........

My intentions are always to blog more. My life is full of distractions. Then when I do have time, I feel like a vegetable. I do not mean that to be cruel before you start thinking of me as insensitive. My brain is mush sometimes and all I can do is sit and stare. I do not have a conventional blog in which I am giving weekly dating advice or reviews on products. It isn't always easy for me to put into words how I'm feeling or what is going on. Sometimes I wonder if you really care. I see some of the crap that falls across the feed of my social media that some of you believe and subscribe to, but yet, you just pass me by. I'm someone who is real. You can talk to me, see me, touch me, pinch me.

As I have mentioned I was pretty ill at the beginning of the year and it has only gotten worse. I have started seeing the docs again, back on a few meds, rounds of labs and blood work, tests,.....as I was preparing to go back into battle, I was putting my binder of medical paperwork back into order. Looking over past lab levels and whatnot when I ran across something that my LLMD had ran that I have not shared with any of my other doctors and I just passed right over. Something detrimental and something that just blew me up against the wall as if I needed anything else.

Highlight-circled-and hand written notes: MTHFR two copies of the same mutation A1289c

Day two:

I am finding myself "nesting". I have been going through from room to room clearing out every corner. As I can. Organizing seems to be the only thing I have any control over right now. We made a trip to the recycle center today. I drug a bench that was in our back yard. As soon as I was finished dragging it a full maybe 10 yards I collapsed in tears in a melt down. Something isn't right. This is the third time in a week this has happened. I'm losing all control. I'm the strongest right now I will ever be. It is becoming painfully relevant.

MTHFR A1289c. I'm born with it. My body cannot convert folate or B12. It is vital for restructure of cells and detoxification. I'm sick on top of sick. Have been my whole life. The Lyme intensifies it. This increases chances of cardiovascular diseases and cancers.


Possible conditions associated with A1298C MTHFR mutations:
  • fibromyalgia
  • chronic fatigue syndrome
  • autism
  • depression
  • insomnia
  • ADD/ADHD
  • irritable bowel syndrome
  • inflammatory bowel syndrome
  • erectile dysfunction
  • migraine
  • Raynaud’s
  • cancer
  • Alzheimer’s
  • Parkinson’s
  • recurrent miscarriages

So, you can only imagine my frustration now as I do not know what is MTHFR related (and yes, it does kinda look like an acronym for something) and what is Lyme related. I'm only left to constantly treat each symptom/disease/condition as I have it. This is a stress factor in itself. 

No one really asks anymore so I haven't shared. My last set of labs showed elevated blood platelets. They've gradually climbed over the past set of labs. Along with a lower than normal body temperature, there is reason for concern. I predict a hematologist in my future. 

You will see me in public. You may see me at the gym. Please be my friend. Do not pressure me into taking a class or pushing myself to go hard. I'm doing the best I can to take care of me. You may see me out having dinner with my husband. On a rare occasion anymore with a friend having dinner. Do not judge me and think I am well enough to go out. No. I am making the best of my time. I want to enjoy life just as much as the next person. You may see me at the store. I may not talk. I may even avoid you. Do not take it personal. I honestly, may not be able to speak coherently that day......I may not remember your name and I may be ashamed. 

On this I close. I'm very saddened currently. My heart is heavy. My life outside of sickness has not been easy lately. I have carried a lot of burden. I have been hurt deeply just this past week and am beside myself. For those reasons you will not find me on the social media platforms you are used to contacting me on.  I have removed myself from them. The emotional strain some of this has taken on me is not conducive to me trying to move forward in reclaiming my health. I may or may not be around here. I am not sure at all what direction I am headed in right now or how long or deep this road is going to be. Blogging may be difficult or I may find it to be the perfect outlet. For only time will tell. 

"They tell me to stay strong, but they don't know what it feels like to feel so weak."




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