RSS

Monthly Archives: March 2012

Should I Have Hope?

I’ve been on the full dosage of the Betaseron for some time now. Amazingly, since getting to the full dosage…and after the first shot of an increase which is never fun….I have felt pretty good! Yay!

I changed from taking ibuprofen 1/2 hour before a shot to taking Tylenol (well, I take generic acetaminophen) 1/2 hour before, then just before bed and then the following morning. This seems to have really helped overall. The acid reflux also has died down a lot. Looking back over the past week+ I can say that I’ve only had a few brief yuckiness feelings in the mornings and then only one day of utter exhaustion. Compared to what was happening, this is way better.

Even though I feel better, this year still seems to be a year of health issues for myself or my daughter. In the past 7 days, I’ve taken her to the emergency room for different ‘possible’ broken bones. Luckily, each time it turned out it was only a bad bruise and no fracture. Last week, she had her fingers taped together. This week, she has a sling. I am hoping that once March closes, our health will be 100% great and not sucky.

Advertisements
 
1 Comment

Posted by on March 27, 2012 in Life, Multiple Sclerosis

 

Tags: , , , , , , , ,

Dosage Smosage

Yea, that is my way of saying I finally got to the full dosage amount of my medication last night.  The first one.  Today I feel like crapola.  I came in to work but it will be a struggle.  I’m just so sick and tired of being, well, sick and tired.  I am so nauseous, lethargic, light-headed, muscles are horribly weak and are starting to become painful all over, and I am just sick to my stomach.  Acid reflux, cramping, sweating, clammy.  You name it I feel it.  Not sure why I bothered coming in.  Driving to work was a joke.  I can’t focus on anything.  I ate something for breakfast and immediately felt like a rock was in my throat.  Geez I hate this.  Hate it, hate it, hate it.  On top of that since starting the medicine I’ve gained even more weight.  I feel like crap.  All over.  My mental state is depressed and teary and I just really, really dislike so many things.  This disease and what one has to go through to ‘try’ to prevent it getting worse really sucks.

MS SUCKS!

Add to all of that my daughter has been getting sick. Last night spent 3 hours in convenient care just to get her finger looked at due to a trampoline incident. Yep, it’s fractured. I sat there feeling worse and worse. Monday I had to work from home because she called me (after I was already at work) and said she didn’t feel good. So back I go home. What a waste of gasoline. So with either her illnesses or mine, it seems like I’m working from home every week at least one day. I don’t mind, but I doubt work is thrilled. And here I sit feeling really horrible and wishing I was lying down in my bed. It is bad enough that I’m close to tears. Yea, I could cry easily if I let myself.

Yea, today sucks

 
Leave a comment

Posted by on March 15, 2012 in Multiple Sclerosis

 

Tags: , , , ,

Why?

These past several days have been rough.  Sometimes I think I can never just breathe and relax.  I wonder if life will ever be one where I’m content, happy, relaxed, and joyful.  I don’t know when the last time I really laughed was.  Oh sure, I’ve done some giggling or chuckling but it didn’t come from deep down and just bubble up in a wonderful, joyful, happy spirit.  So many things are just pressing down on me and I just try to keep trudging along and deal with ‘it’.  That’s all anyone can do, right?  Try to stay strong and take things as they come.   I know I’m not alone feeling like this.  I wonder if the majority of the people in this world actually feel like this and that elusive happy go lucky attitude is only spattered across a small few in the world.

I hate the medicine I have to take for this stupid disease.  It makes me feel like crap.  Why do I have to feel worse every single day than I did before?  Is spending $48000 (yes forty-eight thousand dollars!) a year on one medication really worth it?  Am I worth it?  *sigh* Anyway,  I’m hoping that once I finally get to the full dosage amount and have a few shots under my belt at that level that these side affects (are they side affects?) go away.  Each time I increase the amount, the next day I feel like I was hit by a truck.  My entire body hurts.  Walking hurts.  Sitting hurts.  Lying down hurts. My eyebrows hurt!  lol.  The following day, the amount of ‘hurt’ in my muscles starts to fade but I seem to get the vertigo, nausea, utter exhaustion, feeling like crap day.  Of course I always ‘think’ I will be fine so I head off to work.  Within a few hours I feel so crappy that I have to go home.  I end up lying down the entire day usually asleep or resting.  Then the 3rd day I have to give myself another shot.  The following day is more of what the day before was like but typically I can last the day at work.  I just feel ‘not myself’ the entire time.  It is so depressing and makes me unhappy.  Who wants to feel like that?  I feel  I should just suck it up (that’s what we do in my family…suck it up and deal with it) but it is hard.  So very, very hard to deal with this all the time and all by myself.  Because really, we all just have to deal with this ourselves.  Sure, others may be willing to help but they don’t know how you feel.  They don’t know what you experience.  They don’t know how this disease just totally sucks.  And when it comes down to it, they can’t help.

On top of my feeling sorry for myself (or just fed-up frustration), my mom has been in the hospital.  What was a short, quick outpatient surgery turned into many days in the hospital and she is still there.  She’s not there for any complication of the surgerical site at all.  It was the stupid catheter.! She got a UTI and just guess what it can do to elderly patients??  It can cause dementia and hallucinations.  Yeah.  I never knew that before!  My mom wasn’t herself from this past Saturday evening up through about midday yesterday.  It seems that finally the antibiotics seem to be working on the infection and she is about 80% back to her normal self.  I hope and pray that today she is back 100%.

It really sucks seeing your parent lying in a hospital bed.  I’m lucky that I have both parents living.  I can’t ever imagine them not being here.  I couldn’t ever imagine anything happening to them that they didn’t seem like themselves either.  This week has been a hard lesson.  I’m no longer a young adult.  My parents are no longer in the prime of their lives.  Any day, at any time, something could happen to them or even to me as I’m not a spring chicken.  How much time do I even have on this planet?  How much time for my parents or my sisters?  Unfortunately now I can picture a countdown clock for all of us.  That’s pretty shocking.

I am very thankful that I have sisters that are always there for my parents in any time of need.  Actually they do that for anyone.  They have empathy and caring built in.  As for me, I feel  like a fish out of water in these situations.  I didn’t get the empathy gene I think.  It’s not that I don’t care.  That’s totally NOT it!  I do care.  I just don’t know how to act or respond.  My response is always one of distancing myself and thinking through things logically (if I can) in a moment of crisis or a situation.  My sisters are ones to throw themselves in and help.  I thank them for that.  I’m in awe of them because I don’t even know how to do something like that. I feel so worthless and basically I am with that stuff.  I guess that is why God made us all different with different personalities and traits.  My daughter, luckily, got an abundance of empathy and caring.  She has always been like a mother hen when it is needed.  It makes me so proud.

It’s a downer week.  It’s been a downer year.  This year really, truly seems like it will be a rough one for me.  I will always hope that tomorrow will be a brighter day.  Maybe some day I won’t be so disgusted with my situation.  Maybe some day something will click inside my head to try to turn my health around.  Maybe someday I will have happiness and joy the majority of the time rather than the minority.

Maybe someday

I always say someday.  When is someday going to come?

 
1 Comment

Posted by on March 8, 2012 in Life

 

Tags: ,

 
%d bloggers like this: