Browsed by
Tag: living with multiple sclerosis

5-7 Benefits of owning a pet with multiple sclerosis

5-7 Benefits of owning a pet with multiple sclerosis

I came across this picture the other day Being an absolute dog lover, I had to look for his seven reasons why. Personally I can think of 1 million reasons to own animals but I was wondering what his were. I found his YouTube video that you could watch here https://youtu.be/1JBke_ukVpI. I’d say most of the things I knew but maybe one or two I just never thought of in the same way. I also came across this one https://multiplesclerosisnewstoday.com/2017/03/09/five-benefits-of-having-pets-when-you-have-multiple-sclerosis/….

Read More Read More

A MS anger post

A MS anger post

If you follow my blog you know I’m normally positive. I don’t have the energy to be positive right now. I am so tired of being 46 and having to have somebody cut my food. If I make some sort of protein for dinner, like steak which I recently started eating, my aid has to cut it before she leaves. I could barely even cut chicken. I can barely use one of my stainless steel silverware and usually opt for…

Read More Read More

Running on empty

Running on empty

Man I am beat. I am so tired and I’ve really done nothing but what I’ve done is enough to exhaust me. July has certainly has been a very tough month for me. It started out with my insurance changing to Medicare. Goodbye referrals!!! However, I also had many doctors appointments appointment scheduled because of it. Then I ended up with cellulitis at the beginning of July. July 9 actually was my first trip to the emergency room. I know…

Read More Read More

2nd medical insurance assessment for home health services

2nd medical insurance assessment for home health services

My agency where my aid comes from that I been using for over a year is not acepting my insurance anymore. I have the option to change insurance companies and continue to use my agency or I just have to find a new agency. Right now with my current insurance, I receive five days a week, eight hours a day of home health aid services. I had an assessment last week and where they only offered me five days a…

Read More Read More

High dose biotin

High dose biotin

Since I was in the hospital, this is one of the pills that has changed. First it never made my weekly pill box, which was just a complete oversight. Second, the hospital doesn’t give that out. So I must say I haven’t correctly taken my high dose biotin for a week. It occurred to me, this morning, that this could be the reason I’m having difficulties regulating my body temperature since about Saturday. I finally started taking it again 3…

Read More Read More

High dose biotin

High dose biotin

Since I was in the hospital, this is one of the pills that has changed. First it never made my weekly pill box, which was just a complete oversight. Second, the hospital doesn’t give that out. So I must say I haven’t correctly taken my high dose biotin for a week. It occurred to me, this morning, that this could be the reason I’m having difficulties regulating my body temperature since about Saturday. I finally started taking it again 3…

Read More Read More

You are what you think

You are what you think

This whole hospital episode has put me in a little bit of a depression. I just haven’t been able to shake myself from it but I’m very aware that I’m in it. I don’t know if it is a side effect of the immense amount of antibiotics or if my anti-depressant got messed up last week. I know I ran out and I my prescription was picked up late but I was given them in the hospital. Maybe it just…

Read More Read More

Regulating body temperature with MS

Regulating body temperature with MS

I almost forgot this fact, well slightly forgot this fact. However my multiple sclerosis let me know it is still here in abundance. I got that crazy symptoms yesterday where I couldn’t regulate my body temperature. I’m sitting on my chair inches away from the AC and sweating. Sweat was literally dripping down my neck. Why? I wasn’t even moving. Normally this happens after I eat maybe something a little hot, this time it happened for no apparent reason. Guess…

Read More Read More

Ocrevus and the compromised immune system

Ocrevus and the compromised immune system

I’m happy to report I was discharged from the hospital last night. One thing I know, from my career working in nursing homes, hospitals like to discharge on Friday to make room for the weekend influx. The infection disease doctor would have held me to today but I really wanted to go and the main doctor was for it. So what did I learn from this? First of all this happened from a simple fall. The fall gave me a…

Read More Read More

Still in hospital but doing better

Still in hospital but doing better

I slept last night. That makes a huge difference. I also got them to stop the saline drip that wasn’t necessary and truthfully was torture for an MS patient with bladder issues. I was peeing every 20-30 minutes yesterday. I took a second bladder urgency pill I am prescribed last night which helped me sleep and cut the bathroom trips down to every few hours. I also used a commode next to my bed. It just went smoother. The doctor…

Read More Read More

Verified by MonsterInsights