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Tag: bad ms days

And how are you?

And how are you?

One of the greatest things about my blog, is the feedback I’ve gotten from people that have known me for years. It’s the first time they really seen into my life on a daily basis. The truth is as soon as the how are you feeling question is asked, I immediately, say ok, how are you? I mean really what was I going to say to them, I had an accident today I peed my pants or or maybe I…

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No, I’m not lucky

No, I’m not lucky

There’s a reason I have an aide for eight hours a day. There’s a reason I don’t work anymore. Sometimes I feel like I’m running a scam, that I should be working or I don’t need an aide eight hours a day. Especially when someone says lucky you. Let me explain something to you and myself, I’m not a lucky girl.  I’m not a lucky girl that I’m on full disability and don’t work. I’m not a lucky girl that…

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Damn fatigue a short blog post

Damn fatigue a short blog post

I’ve been so tired lately. I hate this feeling. I have been napping every afternoon for a few months now. Not always a long nap but at some point my eyes just have to close. The last few weeks have been really rough. I’m just wiped out doing anything. I had therapy today. I just am spent. I really want to crawl back into my bed and stay there for the day but I won’t. I’ve blogged everyday since I…

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It’s just one of those MS days

It’s just one of those MS days

It is just one of those days when things are more difficult. It could be chalked up to sleep, I definitely didn’t sleep well last night. Most people would probably blame the weather. I don’t get this one honestly. I find my doctors and therapists blame the weather an awful lot when I have a “bad day”. I get the heat sensitivity one because I live that one but today it is 78 and cloudy. So today it’s blamed on…

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Alpha Lipoic Acid and MS a patient’s view

Alpha Lipoic Acid and MS a patient’s view

On December 13, 2016, I wrote a blog about Alpha Lipoic Acid and multiple sclerosis. On July 3, 2017 this article was published in medical news today. http://www.medicalnewstoday.com/articles/318225.php Ive been talking alpha lipoic acid now for 7 months. I still take 2 600mg pills a day. One in the morning and one at night. Alpha lipoic acid started about 3 months after starting high dose biotin. Another Vitamin shown that in high doses has stopped disease progression. Since both biotin…

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Prozac making a difference

Prozac making a difference

Not too long ago I wrote a post about MS and depression  how there is a link. I asked my doctor to go back on Prozac, a drug I was on for over 18 years. I stopped taking Prozac along with a bunch of my other drugs when I stopped working back in January 2016. I was just taking so many pills to get through a day, I thought by not working anymore, I didn’t need them all.  Well it’s…

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MS and depression it’s not all in your head

MS and depression it’s not all in your head

I wrote a blog couple weeks ago titled am I depressed? https://multipleexperiences.org/2017/05/16/am-i-depressed/. I agree with  everything I wrote, but when I saw my neurologist the other day, we decided to put Prozac back in my medicine mix.  Where I don’t think I’m depressed, what isn’t fully in control, is my emotions. I cry over everything. I’ve written blogs about this too. I cry over happy things and sad things, it makes no difference. According to webmd: http://www.webmd.com/multiple-sclerosis/guide/ms-depression#1 The Link Between MS and…

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The only thing you control in a chronic illness

The only thing you control in a chronic illness

I was diagnosed with MS in 1998. That was over 19 years ago. It’s 42.2% of my life. That’s a long time. There’s only one sure thing with a chronic disease, it holds true with any situation, the only part fully in your control is Your attitude Yes, you could eat right, take the medicine as directed, exercise, not smoke, and not do drugs, these are all wonderful things that may slow down a disease, but it won’t cure one….

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Today was a very disheartening MS day

Today was a very disheartening MS day

This one is not for my family. This is a bad one, so I give you the advance warning.  Everyone’s been telling me I’m doing too much.I am a little stubborn about slowing down. I  been having a lot of trouble at physical therapy lately. I had been fatiguing not just a little but severely and I don’t know why. It’s the same routine I had been doing since November. Luckily, I had my daughter around when I got home to…

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Being Vegan and multiple sclerosis

Being Vegan and multiple sclerosis

May is my going to be my 6th month being vegan. I have had no problems being vegan other than salad dressing and my coffee. I prefer having a carb over a protein any day. How it relates to my multiple sclerosis is a different story: You can’t be vegan and not cook. This has been difficult because my hands fatigue easily making chopping, stirring and sautéing tiresome. The other issue is standing on my feet over the stove. I…

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