I haven’t posted on a regular basis due to my several admissions via the ER for debilitating pain and unregulated high blood pressure. My whole body is in pain all the time, but my left side seems to be exacerbated a little more than the rest. From the extreme joint pain to the burning painful sensations in my left arm. And as of last night, my right arm is starting to have the same burning pain as well. I’ve spoken to my doctors about it and they look at me like I am crazy. One doctor went as far as ordering an xray and a vascular ultrasound of my left arm. He stated that the results came back normal. Now all those who battle incurable chronic diseases know that there is nothing normal about us. Also, I still haven’t received an answer about what is causing the pain in my left side, front to back, under the rib cage. My husband and I feel painful nodules in those areas.
I have totally lost faith in the medical community in reference to my care. I go to them for answers and don’t recieved any. The first thing they do is put pain meds in my i.v. So, now I have reached out to the Sarcoidosis clinic in Philadelphia and a group called “The Grand Rounds”, which is a group of doctors from across America for answers. I provided them with access to all of my medical records which included all films. Both have concluded that my medical care here in my state of Delaware has been inconsistent. Testing that should have been done, wasn’t. And the fact that my physician’s were not communicating with each other, my treatments were not cohesive.
So, as you now know, not only were my doctor’s not listening to me, but they were not really treating me as an unique individual that is very sick.
I have been battling my illness’s for almost 19 years and my health has seriously declined in the last two years. I rely on 24hr oxygen support and the use of a walker to get around. I’ve congestive heart failure twice and a series of ischemic stroke’s and a lacunar stroke. I have been diagnosed with steroid induced type 2 diabetes on top of Fibromyalgia, Rheumatoid arthritis, Chronic Sarcoidosis, Periphial Neuropathy, anemia and Cushing’s. That’s a lot huh?
I am a person battling several auto immune, debilitating chronic diseases. I am fighting for my life. I am a Warrior.
This is a follow-up to the Cinemark Christiana Movie Theatre debacle.
I called the theatre the next morning after being humiliated the night before and spoke to a representative who intern stated that I would be receiving a call from their manager (Stephanie) on Monday. Well that didn’t happen. I called this evening around 4:30 pm and actually spoke to Stephanie herself. After explaining to her how I was treated, she told me “where I was wrong.” She said that I, indeed was sitting in someone else’s seat.? Wrong! I understood the meaning of reserved handicapped seating and I was indeed sitting in a seat that I had reserved. Stephanie also stated that they sat those that was supposed to sit in our seats elsewhere, and that the usher was supposed to tell us this. NOT! LIES BEGAT LIES BEGAT LIES! Stephanie then went on to say that I had no right to raise my voice to her. I rebutted with, why Not? You are not listening to what I am trying to explain to you about what actually happened. She then apologized for her staff not alerting me to reassigning the other moviegoers Stephanie promised me a refund, in which I was prepared to give her my confirmation number so that it could be reimbursed to my card. Stephanie said that was not possible and that I had to come back to the movie theater and show her my digital receipt. Again reiterating that it would be hard for me to do so tonight because of my disability, so may I email it to her. Of course she said no. Stating that I must present the ticket in person in order to receive my refund out of their petty cash fund due to the ticket being purchased via Fandango. She said that it would be okay to send a copy of the ticket with my husband. Stephanie stated, “that if she was not there, then she would leave word with the other managers to refund my money. Hubby went there and the staff denied our refund. A manager named Carlos specifically, spoke very negatively to hubby.
I am venting this because I already deal with being handicapped because of Sarcoidosis and what it has done to my life, but to be humiliated when I was in the right for sitting in a seat designated for the handicapped. Especially, when being asked to move for those who were not. #Fighting4ACure #LivingWithChronicPain #LivingWithAnInvisibleIllness #SarcoidosisAwareness #LivingWithChronicPain #TheRightsOfTheHandicap #Fighting4OurRights #MistreatmentOfTheHandicapped
Flaxseed, is definitely a component saturated in qualities and advantages for the wellness. It’s an all natural material saturated in essential fatty acids and nutrients, supplements, materials, that are required for the correct performance of your body. It’s in a position to reduce sugar’s raised degrees within the bloodstream, hence decreasing our hunger. Additionally, if…
via After I Started To Drink This I Never Did Get Fat Again! I Only Had To Use 2 Ingredients! » Health and Home Remedies — living with fibroblog
At the suggestion of my Rheumatologist that I thought I loved, I found someone who examined me, listened to me, read my chart thoroughly and diagnosed what I kind of already knew. Well, my prednisone prescription was tripled and I am to take, after labs, is a drug that is the next step above methotrexate. Forgot what it was called unfortunately.
Sarcoidosis is now affecting my bones and joints. I called it a long time ago because the pain was extreme, but was told it was the Fibromyalgia or Rheumatoid Arthritis. MRIs and Xrays showed that my lymph nodes were swollen, yet it wasn’t being addressed.
All I ask is for prayers and to all who read this, listen to your heart. If it seems as though you are not being taken seriously, seek out another doctor. Don’t waste your precious time making them rich for doing nothing.