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Tag: living with a chronic disease

Better but exhausted

Better but exhausted

Better today but still so tired. I went into bed at 8 last night and got out of bed after 8 this morning. Today is the first day I’m drinking coffee. Hopefully that helps. However I can feel already my body is exhausted. I did a very simple 30 minute workout because I have a few things going on today and didn’t want to overdo myself. Yet I’m sitting here exhausted. This is not good. So much has gone on…

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Rough day

Rough day

Rough day yesterday. I didn’t feel well when I woke up in the morning. I didn’t pay attention. I did my normal routine and was working out when Minx started eating something he shouldn’t. I reached down to pick up my grabber, which I myself knocked over, and literally fell out of the wheelchair. I got myself right back up but was unable to turn around and get myself back into the wheelchair and slid down again. My body was…

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I have multiple sclerosis

I have multiple sclerosis

I have multiple sclerosis. Sometimes this disease makes it so difficult. I pray for a day that everything wasn’t so hard. Yet one day I’ll look back at days the way I am now wishing I could have these back. That’s the thing, I know in time, it will be worse. That’s a truly sobering thought, knowing for sure my MS will be worse. People ask how I have such a positive attitude, with the real knowledge I live with,…

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Choking on liquids

Choking on liquids

I had 2 choking episodes yesterday. Maybe choking isn’t the exact word because I really just swallowed wrong. The first one was mangos. Cut up in small pieces but slightly hard and very tart, just the way I like them. I swallowed wrong but it wasn’t the actual mango that was causing the problem. The tartness of the piece in my saliva is what I swallowed incorrectly. It caused me to cough, as it should, however I couldn’t move that…

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Jumping from a plane

Jumping from a plane

Good morning. Another week starts again. It is grey looking outside. However the weekend was gorgeous. Open windows and fresh air, I love days like that. Having multiple sclerosis, I like when weather warms up but not when it gets hot. Unfortunately summer is right around the corner and that’s when the bad days will outnumber the good. I don’t have to explain this to anyone with MS, most people have this issue. That’s why I cherish those days with…

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Pain with Multiple Sclerosis

Pain with Multiple Sclerosis

I get these pains, sometimes on my back or my side, out of nowhere. Usually along my bra line. Since I wear sports bras, this is a thicker band area. It always feels like there is something wrong on my skin in a certain area. Like a cut, rash or irritation except nothing is there when you look. The area is fine. No red spot even to show something coming up on the skin. It is completely normal. It just…

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How fatigue affects life

How fatigue affects life

I’ve been so tired lately. I never really took in to account how my body would react to work being done in my place. I knew I would be shifted around slightly but didn’t think it was a big deal. I was clearly wrong. By the time the afternoon comes around I’m struggling to get myself to the bathroom. I’m back to dreading every time the need comes. Sometimes I’m so tired that the hesitancy I talked about recently Bladder…

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The Routine

The Routine

I’m sure I’ve blogged about this at some point because I don’t do well with disruptions. The days of spontaneous activities have long been gone. I could never just meet someone for dinner at short notice. My life, or I should say my activities, are planned both mentally and physically. Everything I do requires a tremendous amount of effort. Everyday is different as to which activity will put me over the edge. The activity might be the same and the…

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My magic button is broken

My magic button is broken

I’ve been chilling in my room as work has begun in my kitchen/living room area. Making things more handicap accessible. Hopefully I will hit less walls with the additional space but I make no promises. Let’s be honest here, my wheelchair driving hasn’t improved. I’m actually waiting once again on a wheelchair repair. This is on the button that was placed on the side that immediately lifted the chair up. My magic button that has been a true lifesaver. I’ve…

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Bladder Hesitancy

Bladder Hesitancy

I’ve written so many blogs about my numerous “accidents” but I never discuss the other way. I actually experience both of them which is why Botox wasn’t an option for me. I dealt with hesitancy long before I dealt with the urgency and the accidents. What is urinary hesitancy mean? If you have trouble starting to urinate or maintaining urine flow, you may have urinary hesitancy. If you ever experienced hesitancy you know how it feels. Your bladder is full,…

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