Foul Weather Mood

Google ImagesIt’s hot and muggy and I’m sick of the air conditioning. So during the day I sometimes open up and leave it off, but I eventually feel wilted and cranky, byproducts of the MS, so in the evening it usually goes back on. Sometimes I gauge my cat’s behavior on whether the air needs to go on: If he’s lying completely stretched out and long on his back and his eyes look glazed, it’s probably time for some cool air.

On this topic, I have to admit that I’m a somewhat moody person. Just like the weather, there are days when I feel sunny and temperate, brisk and aloof, cold and not open to conversation, misty and sad, and hot and volatile. Doesn’t everyone? I like to think that I’m not the only moody person out there, and I do have a way of reigning it in when situations call for it. I think over the years I have learned to better control my emotions when I need to—- something challenging for fiery Aries people who pretty much wear their thoughts and emotions on their sleeves. Nevertheless, I try to make a conscious effort to keep calm and not overreact.

Yesterday was definitely a foul weather day and I know that I lashed out with immediate anger towards a loved one (you know who you are…..) But in my defense, I do keep the dramatics to a minimum, and sometimes people with chronic illness need to just vent and be heard. No replies necessary. And I in turn need to realize that others often also have a lot on their plates (medical, financial, and such) and learn to respond with a little less ZEAL? Is that the correct word?…………Let’s meet in the middle.

4 comments

  • I too have been a bit moody. Now that the PMS has passed I almost feel like a real person again

  • Jen

    Hi Nadja–

    Your Carnival post is so raw and real. I imagine everyone with MS feels this way from time to time. I feel very much like you in regards to guilt (I am still pretty mobile, yet I just won my disability case because I can’t hold down even a part-time, outside job on a regular basis, yet I don’t use a cane or a wheelchair), PMS (I become my worst critic, even though I know it’s hormonal, and all my accomplishments mean nothing to me at this point), and insomnia (the steroids and the attack itself make me so anxious and sleepless, even on sleeping meds, and it takes me about a month to sleep a little better, but I don’t usually sleep well to begin with because my mind is always spinning in overdrive, thinking about what I can and can’t do.)

    Just letting you know that I do understand and it makes me feel a little less isolated hearing you say the same things.

    Jen

  • Todd

    I was diagnosed with MS in April 2006, so I am still trying to get the hang of things. I’ve noticed that lately my emotions swing alot, and it doesn’t take much to set me off. My family notices this too, cause they are the ones who are usually at ground zero. I’m usually really relaxed and layed back, so all this sudden dramatics isn’t any fun at all. I can also get really down at the drop of a hat. I’ve been kinda taking notes and plan on talking to my neurologist about it on my next visit. I’m lso a chronic weird sleeper. Sometimes I can, and sometimes I can’t. I never know when I’ll be able to sleep or not. Anyhow, is that your cat in the picture? I have a cat that looks almost exactly like it. Her name is Freckles. Well, take care!

  • Jen

    Hi Todd—

    Thanks for your comment. What works for me is counseling with a social worker. I’ve been going for a little over 2 years now. After one of my more dramatic attacks, I was completely at a loss for what to do. I was unemployed and uncertain of the future. So I started seeing the social worker and I got on an antidepressant. I went off the medication for about 9 months until recently (May) when I had another attack and again was forced to stop working. I can really tell the difference when I’m on the Lexapro. I guess medication is an individual’s decision he or she comes to with the help of a doctor.

    I also have problems sleeping! I am such an insomniac. My sleep patterns are all screwed up because I have no regular schedule right now. I stay up late and have trouble getting up and about in the morning. Sometimes an antidepressant helps with this as well. You should probably ask your neurologist about this, too.

    I wrote a recent post about MS and emotional counseling. It can be accessed on my homepage: http://www.msfriend.com. I’m glad to meet you and look forward to talking to you again. And by the way, the cat in the photo isn’t mine. I have a large, male orange cat named Sandy. He’s the best!

    Sincerely,

    Jen

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