I’ve been laying in the dark for two hours now. I took some aspirin on top of my three different night meds and am still not able to fall asleep. I can’t shut off my mind and am guessing the small amount of red pepper I had is part of the problem. I wish I could eat red peppers but often insomnia follows, even eight hours later.
So I am sure you have heard by now how a medication, hydroxychloroquine, is stated to help with the coronavirus. As I’m sure you have also heard, this is an anti-inflammatory and Lupus drug. In fact, this is my main Lupus medication.
I called my doctor’s office to see if they could write me a script so I could potentially stock up before it’s all out in my state. They said they could not. I asked about the possible shortage and they stated if my pharmacy didn’t have any, to try a different one.
Thankfully I had a month’s worth from when I was in the middle of switching doctors. But I wasn’t sure if I should take it (seeing the prescription had been a year old) so I called my pharmacist. I asked him if it would be okay and he said yes, especially with the situation right now & that they (my pharmacy) were completely out of the product. “You basically have liquid gold,” he stated.
So, I’m not as worried as much knowing I currently have almost two months worth. But it still crosses my mind. I’m hoping that will be enough time for them to make more to meet demands.
But it pisses me off that drumpf (AKA Trump) stated what he did about the medication. He started a frenzy and it was irresponsible of him. They haven’t even had actual lab trials yet to see how it reacts to the coronavirus! Some people have taken chloroquine which is much more toxic than hydroxychloroquine! According to some Lupus groups on FB, they think doctors have been writing scripts of it for family members and friends to have on them “just in case.” I assumed that is what was happening.
I decided to purchase a picture of Benelli along with my free picture. I wish she had cheaper choices so I could have purchased more. Oh well, I am just thankful I was able to go through the process and receive a free picture. And I understand her pricing. These pictures are on like, a wood (I think?) piece, so it is not a normal flimsy picture.
We hope you are all doing well during this challenging time. Stay safe!
Demons telling me nonsense in my ear
Of all the things I don’t want to hear
Lies, lies, and more lies!
They begin to laugh as they hear my cries
Falling fast down this slope
Searching for something to give me hope
No! I can’t listen to what they say!
Guess I will have to take this day by day
In June/July, a dog photographer put out a FB post stating she was having a contest. A person needed to like her business FB page (Animal Studio Photography) and post a picture of their pet in the comments. Ten winners would win a free sitting session and one free 5 x 7 of their favorite picture. I of course wanted chance to get a nice shot of Benelli since I knew I would never be able to afford one.
Well, we won! 🙂
He did great during the sitting session. He listened for about an hour then after that he didn’t bother trying to please the photographer and I. Haha!
The other week I FINALLY received my free 5 x 7. Here is a digital copy, what do you think??
A few months ago I had a not so normal eye exam. The optometrist noted an irregularity with one of my tests that I take for my main Lupus medication, Plaquenil. That meant the medication was starting to effect my eyes. So my new rheumatologist had me see an eye doctor (ya know, because they want to make sure to see a “M.D.” behind the name) and go off the medication. The new eye doctor said it looked fine so I’m back on the medication for the time being. I go back in for another round of tests to make sure everything is still okay at the end of October.
I decided to change my rheumatologist as I felt my current one wasn’t working enough for my health. I told my rheumy about my symptoms of my Gastroparesis (my stomach is not working properly) and she never bothered to look further into it or to send me to a GI doctor.
The first meeting with my new rheumy went well! He also is seeing my sister for MCTD (Mixed Connective Tissue Disease). It was a relief because I had a “feeling” that he would tell me that I didn’t have Lupus, but have what my twin has.
The second meeting with my new rheumy soon came up and my view on him suddenly changed. He told me he didn’t think I had Lupus but I had a disease called Sjogren’s (sounds like “show grins”). He said the Lupus marker never showed up on my blood work but came up on the Sjogren’s marker. And the Sjogren’s marker can mean the person has Sjogren’s…or LUPUS! Think about that for a moment. He kept asking if I had any seizures or heart attacks and I replied with a no. I think he is having a hard time believing that I have Lupus because I haven’t had one or the other, but the thing is having one or the other is NOT a prerequisite for Lupus! So he ordered a bunch of more blood work. I see him again at the beginning of October but wasn’t sure if I wanted to. Suddenly after 20 years I just don’t have Lupus?? Plus, I have had three different doctors tell me that I have Lupus. So at my next appointment I am going to talk to him more of why I “don’t have Lupus.” I didn’t get any of my thoughts/opinions out when he mentioned this shocker because I was so dumbfounded on what he all said. If I’m not satisfied, I am going back to my other doctors that believe that I have it!