Ramblings · RANDOM · Silly

Team Klaus!!!

This person did an amazing video of them.

I had never watch TVD [The Vampire diaries] before and my dd’s got me watching and catching up on Netflix and on the internet . We watched all 4 seasons in approximately 5 days. I could not turn it off. I am so anxious for season 5. If you love the ‘romance’ and mystery regarding Vampire lore, you will love this series. I’m completely hooked now! Love me some Vampires!

Anger · Craziness · Family · Fear · Health · HELL · Hope · Love · Medical · Multiple Sclerosis · Primary Progressive MS · Ramblings · RANDOM · Silly · Strength

5am… Oh Mr. Sandman!

Nights like these are beginning to piss me off. Mr. Sandman must have lost my freakin’ address. My night has been watching movies and trying to sleep.

I realized after reading yesterdays blog, I really haven’t gotten out of bed for a while now. I’ve been thinking about the ‘why’ I haven’t. If I am truly honest with myself, I know the reason… “What’s the point?” I could get up and sit in my wheel-chariot, but then my ankles become kankles, and I really hate that. I’m no longer able to drive, so I can’t just get up and go out. Unless I have help, I can’t even get out of my bed to get in my chair. So, again, “What’s the point?” I feel safe here. I really hate being out in public. I’m in a body I hate, and frankly I don’t like people. I’m not me anymore.

Some might say I’m feeling sorry for myself. Well DUH! I’m fucking human, of course I do at times. Anyone dealing with a progressive illness is lying if they say they never feel sorry for themselves. It’s human nature. I also feel anger, sadness, emptiness, loneliness, and the list goes on. My body is broken and it’s messing with my head. I try so hard to find the ‘positives’ of life, but when you can’t even sit up in bed without someone pulling you up by your arm, positivity is hard to find. Then the fear sets in. Will tomorrow be the day I wake up and my body no longer moves at all? Every night that thought crosses my mind. I’ve lost 2 dear friends, younger than me, to complications of PPMS. It’s fucking scary. And please don’t anyone say it could be worse! This IS my ‘worse’. Death would be easier. I’m so tired of fighting this all the time. But, I’ve never been a quitter, so death is not an option. But, I’m just so fucking tired!!

I know some of my emotions right now stem from the loss of my mom. But honestly, there’s nothing wrong with telling it like it is… the cold hard truth. So many people with with debilitating illnesses keep their inner thoughts to themselves for fear of what others might think. Yes, I think of death, and how much easier it would be. Will I go there? NO! But, the thought is in my head at times. It’s much healthier to talk about it then keep it bottled up inside. People with disabilities unite!! It’s okay to be sad, it’s okay to feel sorry for ourselves, it’s okay to be angry as hell. We need to vent it out in order to heal our minds. Honestly, if the ‘healthies’ and/or others don’t like it or want to hear it, fuck them! They’re not worthy of us in the first place. You really do find out who your try friends are when illness [serious illness, not a cold 😛 ] strikes.

People tell me all the time to think of the good things; family and my friends who love me. DUH, I know this, but I’d also like a little quality of life. No one but me lives in my body. No one but me feels my emotional and constant physical pain. My body no longer works, I can’t do anything without someone there to help me. My independence is gone. When my kids are in school and hubby is at work and I’m home alone, it’s terrifying. I can’t get out of bed or do anything for fear of falling and hurting myself. It feels like i’m in jail.

There’s a line from one of my favorite movies, Last Holiday, that sums it up. “I would like to be cremated. I spent my whole life in a box. I don’t want to be buried in one.”

I know kind of depressing, but my feelings in a nutshell.

 I’m not getting better. I will keep progressing. Scary part is that progression at this point is heading towards total paralysis. Oh joy!

I am looking in to a new neurologist. After 16 years with the same one I feel he’s getting a bit lax. I’m also looking in to a wheel-chariot that has a reclining and raising option. I’ve been looking for clinical trials for PPMS, but most say the patient needs to be able to walk 20 feet to qualify. Are you fucking kidding me. I even looked in to a trial for incontinence, and didn’t qualify. SERIOUSLY!! I’m the incontinent Queen for fucks sake. If they can help me, they can help anyone! 😉 There’s all kinds of new medications for RRMS. Shit, if they could find a medication for the progressive form, that works, they could control RRMS completely. Get on it you researching fools!!

Well peeps, it’s now after 6am. Think I’ll find another movie to watch. Preferably something boring that will put me to sleep. Where’s my ole economics professor when I need him. lmao

A quick note, I’m reading some cool spell books. Who knows i may be able to cure myself. I believe in the power of nature and balance. Damn, I’ve tried everything else, it can’t hurt to give this a go. I’ll keep you posted.

Ta-Ta for now. Love and Light

Family · Love · Ramblings · RANDOM

No point in chewing through the straps

Hi all! It’s been a while I know. So much has happened. I wish I could say ‘good’ things have happened…

My mom passed away June 5, 2013. Still trying to cope, trying to make sense of it. But, how do you cope? I’m numb, I’m angry, I’m sad. I don’t sleep much as I spend a lot of time talking to my mom, trying to feel her presense. I miss her and am kind of lost right now. I’m not even sure what to type or how to say it. For those who know me, I’m not usually at a loss for words.

I’ve been spending my time lying in bed lately as I have no desire to do anything or see anyone. My way of ‘coping’ I guess.

My sisters sent me a package of things from my moms and I am having a hard time opening it up. I brought home a few things from our last trip up there that I haven’t gone through either. Maybe because it makes it final…

I loved my mom dearly, but we had a bit of a strained relationship over the years. I just hope that when she took her final breath that she knew how much I loved her. I think many people feel this way when they lose a loved one.

Knowing my mom, wherever she is now, she’s taking over and letting everyone know she’s there. She’s probably remodeling, chatting up old friends, and making to-do lists for all. That’s just how she rolled and is probably still rolling.

Mom and me 1999
Mom and me 1999

All I know is I miss her and am hoping she will contact me… somehow, some way. I truly believe in spirits and I truly believe they are all around us. I’ve had first hand encounters before and am hoping at some point I will again.

Trying to be back around more and find my way back to ‘life’. For now I am taking it one day at a time.

Love and Light

Family · Health · Hope · Multiple Sclerosis · Primary Progressive MS · Ramblings · RANDOM · Strength · Stupid Stuff

Feeling a bit nutty…

I know, what’s new right? I’m needing a change, so first thing I did was pretty up my blog here with a new design. Love how WordPress has so many cool options.

Not sure if I shared that I am yet again a foster fail! I suck at it. My worry is, what if the people who adopt him are not good. What if they don’t like the fact that he likes to sleep under the covers or between their legs? I actually had NO choice this time as my hubby fell in love with him. Hmmm, so this time it was Rog who was the foster fail!! HA!! 😛

Sleepy Boy Gatsby
Sleepy Boy Gatsby

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Yesterday we finally broke down and got new tires my on crip-mobile. They were getting bad, but when you have no dinero what can you do. Thankfully, Sears has that deferred pmt plan so we have 12 mos to pay it off with no interest. We’re heading out of town soon and there was no way I would let us drive that distance on ‘iffy’ tires. Especially not with my kids in the car.

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I’m trying really hard right now to focus on other things and fight off the depression. It’s a long hard battle. I usually come out on top, but this time seems different. I can’t quite put my finger on it. Normally I ‘joke’ my way out of it, but nothing seems funny right now. I know it will pass eventually… at least I hope it will!

Peace Out peeps! xo

Anger · Craziness · Family · Fear · FUCK · HELL · Multiple Sclerosis · Ramblings · RANDOM · Religion · Sarcasm

Oh what a World!

Life can seriously get you down.  My newest issue, it’s the fear to go outside of my own home. I hadn’t left my home for months, and last time I left I had a little bit of an anxiety attack in my car. The day went downhill from there. I knew better but my car wouldn’t start my first thought was just stay the fuck home! BTW, if my words a little off because I’m using the speech program as it’s been really hard to type and honestly the speech programs aren’t what they say they are. I do know proper grammar, But sometimes what comes out on here isn’t what I actually said. And honestly, much too tired to go back through and fix it all so please bear with me!

My biggest issue, with not being able to go outside, is my baby sister is getting married in April at her bridal shower is this month. I would never miss it for anything! They may have to drug me to get me in the car to go, but all good as again I wouldn’t miss this for the world.

Wow! As I just read this over there are so many mistakes, and again I am so sorry for them but I really cannot type right now.

I know I’m not feeling well when I just do not want to get on the computer. Facebook is the last place I want to be right now. For a while, I think I’m just going to do some blogging on here and maybe share Facebook but not get involved too much right now as I really need a break, for me. All I want to do lately is to sleep. Depression maybe, yeah think so! I am working on getting out of my house slowly but surely. I actually went out the day after everything went crazy with my husband, and it was a little easier although I did want to get back home quickly!

Unless you have an anxiety attack, a real anxiety attack you have no idea what happens. I am so sick of the people that tell you to just breathe through it. Well you can’t fucking just breathe Through it! I had to leave my room at night out of my cozy bed and asleep in my recliner as my anxiety gets so crazy I do not want to wake up my husband. Then the breathing gets really erratic, start to sweat, the tears flow, and I just want the world to end! If it wasn’t for Valium I probably would’ve pulled all of my hair out of my head!

I hate how this affects my family, but it’s so hard to just let it all go. I try to keep it to myself, but it’s very very hard to do so. I know I have love I have friends and family, but in all honesty most people don’t want to hear about it. Most people don’t understand what it’s like to have your life taken away from you and end up in a wheelchair. Unless you’re in that situation, you really have no idea.

They say things happen for reason, I think that’s bullshit! If it were true then all of the murderers, the pedophiles, and scum in prison, would be stricken with these illnesses. So I’m sorry, but fuck that bullshit that things happen for reason!

Does it sound like an angry? Well I am angry, what’s going happen when the day comes that I wake up and can’t move,  I wake up and can’t speak. Who is going to help then, God! I don’t think so.

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Peace out kids!