Showing posts with label medication. Show all posts
Showing posts with label medication. Show all posts

Wednesday, August 26, 2020

I Feel like I take so many Medications

                                I'm Sorry It took me so long to get this out there. 

                              I've just been going through a lot with these relapses.

         Although I'm sure there are people that take way more! I just feel like I take too many.

  

 This was the original thing I wanted to blog about for the past few weeks or so. My body has been having what's considered a relapses they've been preventing me from doing so. And I was giving yet another medication. Which helped at the time. Yet, at right now I'm not so sure being that there's still other issues going on 😢.

  With that being said I don't take as much medications now but I still take enough. Which is why I’m not taking as many now( no vitamins😕).

 Now I take 5 sometimes 6 (if I’m in pain)prescribed medications(pills) and two different prescribed eye drops )in the morning. As well as 2 allergy pills. In the afternoon I take 3 prescribed pills. In the evening I take 5 prescribed pills. Three days out of 7 I have to give myself a needle(I really hate this part).

And I was taking vitamins on top of it. Yet, I ran out of them since I originally started this. So, it doesn't seem like as much now. If you all have been keeping up;you know the only income I have at the moment is saga, which is literally only $219 a month, I can barely afford to survive as it is. 

  I was only able to get the vitamins when I got my stimulus check. And I didn't purchase enough to last a long period of time. 

 If I had the vitamins in the mornings it would be two more. Being that I’ve ran out I haven’t been taking them. There's also another 2 maybe 3 that I didn’t even lost; being that they’re as needed. One I may take more than the others.

 I didn't  go into the names of all of them and the dosages. Being that I'd probably be here all day. Trying to explain them all , and what they are for.

 I'm sure it sounds like I'm complaining. It just tends to get overwhelming at times. I just had to get that off of my chest.

Yes, it took me forever to get this out. Blame the relapses 😂.

Do you take a lot of medications? Or not a lot at all?What are you thoughts on this? 

If you have any questions don't hesitate to ask in the comment section. And Please don't forget to follow and share this blog! It would be greatly appreciated.


Wednesday, June 12, 2019

This is week was a good week

 Health wise this was a great one. I had a migraine here and there. My migraine pills work most times. Other times I have to take Motrin or Aleve  to ease them. I actually just took two Aleve pills.
 
   It would probably be nice if I could take Tylenol like most people. Having allergies to certain stuff really sucks.   I'm just happy I don't have to walk around with an Epipen like a lot of people.

 Those of you that do make sure you always have it on hand.  Although last week I woke up with hives. And I have no idea what caused it. I kind of wish I had one then.I sure took them Benadryl  pills as fast as I could. The children's Benadryl would have worked even faster. There's no little babies around us so that was a no go.
 
 I think this particular migraine is caused by me stressing. I have bills that I can't afford to pay. So i'm concerned with how that going to get done. As well as i'm searching for something at the moment that I'd rather not talk about.

I mean you guys already know some of the things i'm searching for (housing, part time job, and how i'm going to keep this storage and phone bill paid). This is just something I'd rather not disclose at the moment.

  I have been applying for jobs. I'm either nowhere near the location. Or don't have a qualification or two they they're requiring. I wish I hadn't been denied my med card. Otherwise I'd be burning the road down in somebody's bus or company vehicle.

  Me driving for a living was kind of relaxing at times. When I was able to site see. And not have to focus so hard on the road and directions. And when I got lost lol. That's what my aunt and I act as though was a game. Even when we were really lost a couple times.

Anyway this migraine is still not easing up.  Even after me taking the Aleve. I'll try to write again later on this week. I just figured I'd come with an article today instead of more pictures and videos. Hopefully you all are or have enjoyed your day!

Sunday, May 19, 2019

Surviving Multiple Sclerosis/ help and mental health


      I’ve happened to notice a few things. Over the past couple of months. People say when you need help to reach out. If you don’t speak on it no one know. When is it that when people do they turn a blind eye to it? Which takes a lot out of people because it is really embarrassing.
  Not everyone feels that way. And I understand that some people aren’t in a place to help. It just has me thinking some people end up in even worse situations because of it.
 Whether it be from friends, family, or even programs that are out here to(help) people.
 The programs that are out here to help people have many clauses. And to me most of them don’t make any sense. I sit and think on why people tend to go out and harm themselves and sometimes other people. Now, I understand some people tend to lie about things. Not everyone is built like that.
 A lot of people myself included really need help. And the only way to get them is to be an alcoholic, a drug addicted individual, or to live in a dangerous shelter(yes, I said that).
   Where is the programs for people like me; who can’t get assistance from the state except food stamps and medical(awaiting a disability decision)? What kind of help is really out there?
  I’ve applied for part time jobs. Although I don’t have that many degrees/certificates. The ones I did obtain in the past can’t be utilized. I previously held a Certification Nurse Assistant certificate as well as a commercial drivers license(class b with several endorsements).Both expired one because I hadn’t utilized it in years the other because my current health condition wouldn’t allow them to approve me to work.
Who really wants someone with Multiple Sclerosis(that occasionally has flare ups) driving them around or caring for sick individuals?
  I can’t go back work on my Associates degree, start any program, because I can’t do all of the hours. I’m limited to 20 hours. Which I’m unsure of whether or not I can actually do that. With me having weakness, numbness, tingling, and my leg sometimes giving out on me.
  Is it that people really don’t care, can’t, or won’t help people in positions like mine? Things of this nature really can have a hazardous affect on people’s mental health. Or does that not matter when people aren’t actually taking medication for it? Or not seeking professional help for it?
   I take enough meds already and would rather not have someone judge me any more than what they already are.
  I’m using these blogs and my YouTube channel to vent, gain insight, and eventually gain some type of income. As well as to help myself deal with my multiple sclerosis as well as other people.
 I am on sites: vocal media and  YouTube .Links provided if you have a moment check them out!


 https://vocal.media/authors/tatiana-littlejohn


https://www.youtube.com/channel/UCOzvODbsdT35sTb4bcpj8VQ?view_as=subscriber



Friday, May 17, 2019

surviving Multiple Sclerosis/My Medication

  It is a needle a have to inject 3 times a week. It comes in a prefilled syringe. Sent to me once a month. When I was diagnosed it was highly recommended by my neurologist. And I absolutely hate it. Even though it helps prevent me from having major flare ups. They seemed easier to manage in the beginning.
   I have really light skin and I almost always get red marks. Every so often I get sores at my injection sites. And before you ask Yes, have to inject myself. I’m able to stick it in my thighs, my stomach, the meaty part of my arms, and my butt. Although I usually use my stomach and my thighs. It hurts me when I use the other sites.
   Being that last month I got a sore on one side of my stomach. Which had me using antibiotics for a week. And still has me sitting here with a scab. On Saturday I noticed another sore coming on the other side of my stomach. It really sucks and is painful.Also not cute at all.
 Today I decided to start using my arms as well. It hurt like hell. And I can’t see it at the moment I’m sure it’ll be red when I’m able to look at it. I go to see my doctor next month and I’ll have to tell him about it. If it gets any worse, I’ll have to go and see him a little bit earlier.
I’m writing about it today because I’m sitting here ready to cry about it. He told me the last time I saw him that he may have to make a change to my medication. I’m not sure what to expect with that one. I actually never took the time out to research other medications. What are some of the medications you’ve heard of or take?
  So, I don’t know if I’ll end up with another needle for a shorter period of time. Or some type of pills. I’m about tired of those because I think I take too many already. Although being a Certified Nurse Aide as well as Medication certified(working in a group home). So, at one point in my life I’ve seen people have to take way more medications than I take now. I think its just that fact that I have to take them period; Is why I am even making a complaint.
  It has me wondering if I had never ended up with Multiple Sclerosis would I have still had to take all of these pills? Would I being going through the aches and pains that I experience? Or the hospitalizations? Would I have ended up out of work like I am? Or even living from couch to couch like I am?
I’m to the point were is frustrating me.
  I’m also feeling like it’s taking forever and a day for me to get myself out of this situation. Like I’m making people uncomfortable in their own homes. And the shelter is an option but I’m afraid to go.
   I got a call the other day about an article on the one I’d have to go to. So, I started looking at other articles about the place. One stated someone had gotten stabbed there about two weeks ago. Then about the staff mistreating the people forcing them to sleep in chairs. As well as them having all types of drug addicted individuals and alcoholics around there.
 I mean with the way I’m getting sores that are becoming infected already; I’d probably end up with an even worse infection.
I said all of that to say I hate taking my needle. Even though I’m still going to take it.