Recently I have been writing, but not what I normally write. For some odd reason I have switched to writing poems, or at least, trying to anyway. I am not sure on the sudden shift but I am just going to go with it. Here is a little poem I wrote and am finally putting out in the world. Thanks to my sister for being my beta reader. 🙂
In a recent blog post (now I will have to go back and check) I stated that I had been having horrible heartburn. On my worst days even peanut butter and water would give me heartburn, which made trying to figure out what to have for the other meals a tad difficult.
I decided that I finally had enough trying to deal with it on my own so I made an appointment to see a GI doctor. The GI’s office called and apparently I had already seen one of their doctors for when I had gallbladder issues. So they booked an upper endoscopy for me at the beginning of January.
It had been a while since I’ve had to spend time in the hospital so naturally I was nervous as hell. I started crying when they went to put in my IV. If I have to have anything medical done I cry. I hate it and you would think I would be used to it after all these years dealing with my Lupus. My mom once made the comment that perhaps the reason for me being hysterical is that I had to do all this testing when I was just a kid/young adult and it somewhat scarred me. I think she is right.
Later, I awoke in my room and asked the nurses what they found. I was told that I have Gastroparesis which meant my stomach was not working correctly by not completely emptying. They changed my heartburn meds and told my mom (since I was coming off the drugs) to call the office if things didn’t change.
I was told nothing else so I had to do some online research, which is ironic because normally doctors do NOT want the patient to do that. Suddenly things began to make sense. I had been experiencing some of the symptoms (nausea, the constant feeling of being full, no appetite, and heartburn) but I just thought it was my Lupus.
The new medication had helped the first month or so but now I am starting to get really bad heartburn again. It looks like a diet change is in order, which should be interesting because I am already a finicky eater.
I have been away for quite some time as some of you may have noticed. I’m hoping to post again soon to explain what is new. As I look out my large living room window, I see snow zooming across. It’s somewhat blizzard conditions today so I figured I would post some flower pics to remind myself that Spring should be here soon. They are from a birthday bouquet but that is besides the point. It’s flowers!
Since I normally have insomnia, I love sleep. I love bedtime. I know to enjoy it when I get sleep because there is a good chance that I won’t get any the next night. However the last two to three months, I have hated sleep because my whole backside ends up in such pain every night. I wake up with a headache EVERY morning and the intense pain radiates down my neck and continues all the way down my back.
At first I thought it might be my new mattress, but it was past the return date so I couldn’t bring it back. I did some more thinking and also thought it could be my Fibromyalgia. I know talking with one of my aunts that she no longer sleeps in a bed because of her Fibro pain.
I decided to experiment one night and slept on my new couch, which mind you, is a comfy couch during the day. I found when I woke up, I had the same familiar pain. So I know it is my Fibro. This is the first time I have had issues from my Fibro and sleeping. After talking to a friend that also has Fibro, she mentioned she has dealt with the same issue and a zero gravity chair works great. So until I can save for a zero gravity chair to sleep in, I need to figure out something else.
On Monday I saw my family doctor and we decided it would be best to up one of my doses instead of adding another new pill to the mix that I already take. It should be at least a couple days before I can tell if the extra pill is working or not. So now I wait…
I’m not sure the last time I posted three times in one day, or if it has ever been done by me. Luuuuuuuucky you!! 🙂
I still have been spending an obnoxious amount of time coloring in my free time. I happened to look at some of the books I colored some time ago, and got a warm, and fuzzy feeling seeing that I have improved. My shading has gotten better as well as coloring hair, yet I still struggle with those two areas.
Benelli is doing well and will be turning one at the end of this month. If it’s not too humid and hot out, I try and take him to the dog park to get used to other dogs. Buuuuut, he is a chicken and just drops to the ground to submit. Haha! Maybe one of these days he will surprise me and play with a dog.
What a week! I had a very busy week so I was not able to blog. I have been slowly increasing the number of drops every day; tonight I took 18. I know it will be a little over 30 days until I am finished with the bottle, since I haven’t been taking the full recommended amount of drops per day. *Fun fact: there are 1,000 drops of CBD oil in a Hempworx bottle.*
One thing I have noticed is that I feel better when that special time of the month comes around (Men: skip the rest of this paragraph). I still get cramps, but they are soooooo much easier to deal with. Another plus is that my nausea isn’t as bad compared to when I’m not on the CBD oil.
Another thing that I have come to realize is that my IBS (irritable bowel syndrome) has calmed down. Don’t worry, I will spare you the details! 😄 Haha!! Just believe me when I say it helps with that issue.
A couple days ago, my arthritis in my left knee was letting me know that rain was coming. With an achy and painful knee, I had to completely use the rail along the stairs to be able to get to the top. I’m talking putting what weight I could on the rail while using my arm strength to pull me up each step. When I finally got at the top of the stairs, I took 3 drops of the CBD oil and rubbed it on my knee. I then went to lay down and found out an hour later that it helped! 😃 I still had some pain but it was much tolerable, plus I could actually walk!
I’m dreading when this bottle becomes empty because I can’t afford to purchase it. 😞 I don’t want to ask my parents to help because they’ve done enough for me. I’m not looking forward to once again dealing with the full force of my ailments.