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Tag: ms symptoms

Up all night and it wasn’t a party

Up all night and it wasn’t a party

ALL NIGHT!!! I may have slept for twenty minutes at the most. I know at some point my dogs started playing with each other like it was the afternoon. One of them was sick, I was cleaning up my floor at wee hours of the morning. I was crying because when I’m that tired and can’t sleep I get very frustrated and cranky.  I can’t take not sleeping. It’s just the worst thing that could happen t me. It’s this…

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Perseverance, persistent or just plain stubborn

Perseverance, persistent or just plain stubborn

I don’t know which one I am take your pick. If you haven’t read my post for the last couple of days, I had an incident. I slid to the floor and I wasn’t able to get up.  One of the culprits could’ve been the fact that I increased one of my medicines, Gabapentin which is the generic form of Neurontin, due to the pain in my shoulder from tendonitis. I increased it on Sunday, and the incident happened on…

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Yesterday was a very disheartening MS day explanation

Yesterday was a very disheartening MS day explanation

First I want to thank everybody. I had a lot of support from a lot of people and I can’t say how much it meant to me.   There were a few contributing factors that went into yesterday that I wanted to explain. First was my mood. I was very stressed over an email I got the night before about my daughters housing for college. Her housing agreement had to be signed and returned to the school within five days…

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Bears hibernate in the winter, MS patients hibernate in the summer

Bears hibernate in the winter, MS patients hibernate in the summer

Got a wake up call the other day. We went from a comfortable 60° in New York up to  82° overnight.  Silly me, didn’t think anything of it and opened all the windows.  I have roughly 7 windows in my apartment that I opened, well I should say my daughter before she left.  Normally there’s a nice cross breeze in my apartment, but that takes wind. I live upstairs, heat rises, no wind, so no cross breeze and by 2:00 it…

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The evil art of future tripping

The evil art of future tripping

I was future tripping yesterday. A very evil thing to do. Future tripping, in my world, is when you worry about what’s going to happen in the future when you really have no idea. So you get your all worked up over a possibility but not an actuality.  I future trip over the same three things in my life; my multiple sclerosis,where am I going to live  or my finances.  I work hard at NOT doing it but one of…

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My current list of medications for my MS

My current list of medications for my MS

With any chronic Illness, I think our medicine cabinet becomes a small pharmacy. I thought I’d give a list of what I am taking for my multiple sclerosis, the dosage and the reason. I’ve included links to my other posts if I have information that I thought was useful on a particular drug or vitamin. This post is an added plus for me. I can print and give to doctors instead of rewriting each drug I take on their medical…

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My multiple sclerosis affects everyone

My multiple sclerosis affects everyone

I’ve written blogs about this in the past, my daughter at 17 takes on the bulk of the responsibility. It’s not something a 17-year-old signs up for, and she’s been doing it for years.  My mother takes on the brunt of the emotional side of my multiple sclerosis. Another topic of my blogs that you could find throughout. My step dad takes on the emotional backlash of what my mom takes on, breaking his heart. Plus he’s the one taking me to…

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Who wants to date someone with multiple sclerosis?

Who wants to date someone with multiple sclerosis?

I’m afraid to date.  I’m afraid to be rejected again. I’m afraid to be hurt again. I’m afraid to fall in love again. I’m afraid of the pain. I’m afraid to have to explain the embarrassing MS symptoms again.  I’m afraid of the embarrassment again. I’m afraid of the anxiety again. I’m even afraid of the excitement of it again. I’m afraid of the hope of it again.  I’m afraid of the beginning, the middle, and the end. I’m just…

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A multiple sclerosis life coach

A multiple sclerosis life coach

When you go to group meetings on the specific subjects, normally you talk about that subject. When I joined my MS support group,  I guess I thought it would be more of a round circle kind of discussion group. I’ve definitely have walked away with information that is very useful.  I’ve made friends that have been a wonderful additions.  I just thought it would be more of a support group of people talking of issues, frustrations and feelings. I didn’t…

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Migraines with multiple sclerosis

Migraines with multiple sclerosis

This is the strangest topic with multiple sclerosis because migraines themselves are a very tough thing to medically see and explain. Migraines don’t show up on any MRI, blood work or Cat Scan. Doctor’s go solely on the patients account of the symptoms. The National Multiple Sclerosis Societyhttp://www.nationalmssociety.org/Symptoms-Diagnosis/MS-Symptoms/Headache  says this about headaches: Although headache is not a common symptom of MS, some reports suggest that people with MS have an increased incidence of certain types of headache. One report noted…

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