Monday, November 16, 2020
Friday, November 6, 2020
It's hard enough for the individual with a disability already. So, for them to try to explain things to you ; and you to brush them off and act as though you don't care is heartbreaking.
Please don't tell them what someone else is going through. Nor what it is they are doing. I'm sure they wish they could be in that person's position. Or something close to it.
I'm typing this because I've tried different groups online years ago. and I didn't like how it was going. And per my therapist, I tried again. Upon doing so I realized that just like we could go in and get support, our friends and family members can too, and in some cases should.
To get a better understanding of what it is our diagnosis entails. And I don't mean just for multiple sclerosis. There are different types of groups out there for everything.
You just have to research and find the right ones. And I urge you guys to do so to get a better understanding of what it is your friends and family members are going through.
Wednesday, October 21, 2020
For the past few months, I've been complaining about pain. And I have not been able to see any of my regular doctors. Only after making a complaint was I able to have them get in direct contact with my neurologists.
And he's a little bit older now. So, I think I may have to start looking into getting a new one. Being that all of the last few appointments he's only been consulting via phone.
My primary doctor hasn't been in at all. And they've had another doctor stand-in. And I automatically didn't like his vibes. Being that I could tell he hadn't even looked into my files.
Offering me some meds without even taking into consideration that I have a therapist. And has offered me psych meds several times. Like, don't you think of have maybe been prescribed them by her if I’d needed them already?
Then I've been describing my pain to him over time and he's been kind of overlooking it.
Now I know I have never allergies to certain things. As a doctor, if he's unsure about what to prescribe me; shouldn't he be trying to refer me to someone else? Instead of telling me he couldn't because my Neurologist had given me something else. but had only given me enough to last to my last appointment.
An appointment that the messed up and had to reschedule. A month out mind you. Only to tell me to make an appointment with him for him to still ignore my issue.
And then give me a referral to pain management after me emailing them about their incompetence. Which still resulted in me not getting in pain medication.
At this point, I see why some people's health goes down the drain. And it a very scary site!
Have you experienced this? What do you recommend? Do you find doctors by word of mouth or your own research?
I really need help with this. Please leave your thoughts in the comment section. And also don't forget to follow me!
Sunday, July 19, 2020
Thursday, April 16, 2020
Infusion Day If you click on the link above it'll bring you to a Youtube short video. From the day of my first full infusion. Which...
I noticed there’s a lot of people don’t go to the doctors often. Unless they’re sick. Sometimes they go when its a little too late. Which...