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Tag: difficulties with ms

MS views a news round table discussion

MS views a news round table discussion

I’m attending a discussion group today for people with multiple sclerosis or care givers of people with multiple sclerosis. It’s a round table discussion group that is lead by two different MS doctors. Many years ago, I was a patient representative for the drug Gilenya. I use to tell my MS story to a group of people either before or after the guest doctor would discuss MS and how the drug worked. I must admit it was a lucrative deal for…

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Drink yes, drunk NO

Drink yes, drunk NO

Well found another thing that can no longer be on my list of things I can do, get drunk. Since the last time I actually consumed a lot of alcohol, other than wine, was over 2 years ago, I had no idea. I went out for dinner with my friend last night and had a very, very dirty martini, my new drink choice. No big deal if I had one, might not have been an issue if I stopped at…

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Was MS present long before my diagnosis?

Was MS present long before my diagnosis?

I’m pretty sure I had a MS long before I was diagnosed . I had many strange things happen even as a child. When I was in the fifth grade, I got it rash.  The rash was only on my hands and my feet, like gloves and socks. The day my mom took me to the dermatologist, I  threw up in the bathroom. The dermatologist said I was having an allergic reaction to the virus. My body was literally allergic…

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tips for dealing with the heat with MS

tips for dealing with the heat with MS

I’m hibernating for the summer. For most people with MS heat is very difficult. It causes fatigue and muscle weakness, spasms and it basically exacerbates all your current symptoms. They make a cooling vest but let me explain what this thing is. First it’s a vest that comes up to your waist so if closed will nicely accentuate your hips not very flattering. Second it’s this light brown/tan color that is just plain ugly. Third the vest has something like…

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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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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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I am never getting a handicap van

I am never getting a handicap van

So I had to take my mom and my stepdad to the airport yesterday. We were driving my black Honda Civic two door. His name is Bob. I name all my cars.  Everybody was trying to tell me you should not get a two door car, you have too many devices that need to go in the car for your MS. They were all right. I really should not of gotten a two door car. However he’s so beautiful and sexy,…

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Starting the process of getting an aid

Starting the process of getting an aid

Good morning and happy Friday to everyone.  Most of the time I dictate my blog through the voice on my iPad. Then I go back and correct any mistakes, which are usually a lot and sometimes hilarious. What obviously never comes across is my voice inflections when I’m speaking, probably why my humor doesn’t come across. I guess you can’t hear sarcasm in words that you read. Oh well, back to my topic, which this morning is, that I started…

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