Since about 2012 I've been living with Multiple Sclerosis. And In 2018 it was the reason I had to make some major changes. I started this blog to share my experience with that and other things. And maybe get some insight. To help myself and other people. along the way.
Showing posts with label Youtube. Show all posts
Showing posts with label Youtube. Show all posts
Tuesday, January 12, 2021
The Last Video I Made/ Regarding my natural hair
Hello Everyone,
I realized it's been a little while since I've posted anything. I posted this video a few weeks ago on Youtube. Yet, I did not share it anywhere. Although it is an old video I really wanted to share it here.
My hair has come a long way. Well, I think so anyway. Being that I am so used to perming my hair and putting heat to it all of the time.
I can no longer do my hair myself. Being that I've been having issues with my hands. I'd like to share the fact that I did however utilize the treatment CardiB shared before(a mixture of avocado, banana, castor oil, mayonnaise, 2 eggs, honey, and argan oil ). I wish I could find the original video from when she made it. . And I believe it has helped me strengthen my hair along this natural hair journey.
Now it's not long as ever but it has I think gotten back to my shoulders. After several sets of braids.
This is From when I first cur the perm and the dead ends off.
This is the second set of braids I had gotten done.
This is the last set of braids I had done.
I'm broke so unless someone is nice enough to donate to my cashapp (over on the right). My hair will be looking a hot mess. The braids I did have my aunt and my gramma was nice enough to pay for me to get done. And I'm not sure they'll be nice enough to do so again.
This is when I did the hair mask.
And this is where I am now.
Please keep in mind I'm able to get my blogs done either utilizing one hand(so, it takes me some time). Or speech to text.
If you've taken the time and read this far in, thank you, I really appreciate you, and I hope you follow and or subscribe to my blog and my Youtube page!
Wednesday, August 26, 2020
A 4-Year Old Taught Me How to Live Life by Brett Holcomb | Brett Holcomb...
Pay attention to your children. The things that they do can sometimes apply to your life!
Monday, August 17, 2020
Saturday, August 15, 2020
Blog and Video Update
Something else got in the way in regard to my health. I will be posting a video. It will be posted by the end of next week. I did start on the blog( honestly I started it two weeks ago). So, I will try to edit it soon. Please bear with me! Keep me in your prayers I'm trying. My health is just getting in the way. The relapse part of the multiple sclerosis is definitely getting real at this point!
check out this TikTok video for an update for now
Saturday, August 8, 2020
Tuesday, July 28, 2020
Sunday, July 26, 2020
Wednesday, July 22, 2020
Even A Little Bit of Support Goes A Long Way
Don't Expect me to support any of your endeavors;If you've never even took the time out to take a sneak peek into mine!
Monday, May 18, 2020
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!
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!
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Tuesday, June 11, 2019
Sunday, June 2, 2019
Re-posting this post Re-edited blog/ About My second attempt at this
So,I started what I assumed was a blog before.On Vocal Media but I've since deactivated that account. After I'd posted three different articles I realized that wasn't the route I had wanted to go.On that site.
I assumed I'd get more traffic. Not really sure exactly how I was going to do so. I shared it on my pages. Several times might I add. I'd even sent it to few friends and family members look at it. I'm assuming because it might of been a little to real(I've been and am still going threw some things in my life as well as with my finances); not too many people gravitated to it. or they just didn't care.
The site itself was okay I guess. A great starter for me. It pushed me to look further into things.
Which led me here. I didn't like how the payouts were listed on that site,after I got to my third article, and realized at that rate I'd never get anywhere. Nor to get my stories out like i'd like.
I assumed I'd get more traffic. Not really sure exactly how I was going to do so. I shared it on my pages. Several times might I add. I'd even sent it to few friends and family members look at it. I'm assuming because it might of been a little to real(I've been and am still going threw some things in my life as well as with my finances); not too many people gravitated to it. or they just didn't care.
The site itself was okay I guess. A great starter for me. It pushed me to look further into things.
Which led me here. I didn't like how the payouts were listed on that site,after I got to my third article, and realized at that rate I'd never get anywhere. Nor to get my stories out like i'd like.
Although I did like how it allowed for people to give tips. Something about the sit itself didn't sit well with my spirit. Which led to blogger and eventuality my own website . Were I signed up for ads , added my cashapp,and also my paypal links. That way if people would like to donate they could .Or they could just click on and ad or two.
Again that was is my first time actually blogging and can assure you it wasn't my last. I have a YouTube page as well (Mz Littlejohn) you can look at what I've shared there as well.
Again that was is my first time actually blogging and can assure you it wasn't my last. I have a YouTube page as well (Mz Littlejohn) you can look at what I've shared there as well.
I hope that I can be a help to someone as well as myself in doing this.
I hope you enjoy and continue to hang in here with me. Have a great day.
MzLittlejohn
MzLittlejohn
Thursday, May 23, 2019
Surviving Multiple Sclerosis/Contest entry
I entered a contest today. It's called the 25k Pitch competition. Started by Chamillionaire, E40, and Republic.co on a website named Convoz.
I'm not sure If I'll actually win. Although if I do I hope that I can make a difference in peoples lives To try and get them the help that I can't seem to receive. If you've read any of my prior blogs on here, my Vocal Media account (https://vocal.media/authors/tatiana-littlejohn ), on my YouTube account ( https://www.youtube.com/channel/UCOzvODbsdT35sTb4bcpj8VQ ). I tend to talk about the struggles i'm currently going through.
After being hospitalized the end of September. My children and I being separated and losing primary custody of my youngest son. As well as about me having to living from one house to the other. To the point were I may end up in a shelter next.
Hopefully I win and can get the help that people in these or similar situations need.
I only came back up here this even to post this. I hope you all are having or have had a good 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
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.
Surviving Multiple Sclerosis/ My parents, family, and friends
Yesterday
evening I was in my feelings about my medications. This morning I am not any closer to
getting out of them.
For some odd
reason I haven’t been to sleep. I broke night. And when I crash, I’m not going hear
anyone. This morning my oldest started texting in him, his sister an I’s group
chat. About our cellphone bill. Upon
doing so I realized we’ve ran into yet another controversy. I say we but at
this point it is on me.
As of right now we’re
all separated. And he’s the only one with even a little bit of income. His paycheck
would leave him with nothing after paying the rest of the bill. Which means I
have to take on the task of trying to get money for the rest of the cellphone
bill, our storage, and how the heck we’re going to get my daughters things from
her College to our storage.
And of course, being
that my parents have been holding me down financially . The only one that I
could think of immediately is my dad. Who’s been thankfully helping us out a
lot more. As I type this I’m crying.
The both of my parents may not have much; but
they help us as much as they can. Even though it’s not even really their responsibility.
I am so grateful for them and it’s not even funny. I don’t know what I would do
without the two of them. This is one of the most devastating times of my life.
Now I’ve gotten help
from a now old friend; that this situation of mine has caused me to fall out
with. As well as much Auntie; and my best friend( who I’m sure will probably
say she hasn’t done anything),and she’s done more than she thinks. Even though
the situation isn’t ideal. Heck and in both cases I probably shouldn’t be there.
But they’ve been a great help as well. Surprisingly in my old friends head I was ungrateful. Even after
expressing almost every chance I had gotten that I was very grateful.
I say I’m crying, and
I mean I am really sitting here crying as I type this. I’m beyond overwhelmed
and am tired of having to lean on anyone. I’m not used to this crap. It’s has
me questioning a lot of different things. And also asking why when I know I shouldn’t. I had been working since I
was 15 years old. It hurts me deeply because I can hardly do much .With these
flare ups I have going on. Today it’s the shakes(great)
I’m just happy that I do/did have anyone in
our corner. I can only imagine how people that have no one at all do this. This
is a burden I wouldn’t wish on any one at all. How do the people that do handle
it? What do they do in times like this? Do they speak to counselors The two I
spoke to weren’t very much help)? Or psychiatrists?
I’m sure me speaking about things I’m going
through has everyone looking at me sideways. This is the point in my life that
I really don’t care how anyone feels. Especially if it isn’t from my children,
my parents, and my friends that have actually been through this with us.
Hopefully you all
will see this. When you do just know you’re appreciated! Thank you for holding us
down when we couldn’t.
If you’ve taken the
time out to read, please share and donate if you like. I hope this helps someone
other than just myself. It helps me by getting all of my crazy thoughts out of
my head. Instead of holding the pain and suffering that I’m enduring in.
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