Posted in Chronic illness, Health

A future in the balance

It’s been roughly eleven years that I have been diagnosed with RA. I have experienced many flares that bring excruciating pain and I have been rendered nearly unable to function in today’s day to day life. But, I have also been blessed with times of remission, and nearly pain free periods. Those are the days when I give special thanks and where I’m grateful and in tune with my surroundings on a different level. I already am, but even more-so then and those days become a precious gift.

The pain never goes away completely, but after a bout of flares, the remission periods of little pain become much more tolerable. It is usually the winters that are tougher, and I have frequently referred to myself as the human barometer. I can pick up on approaching storms, and the pressure changes make my bones heavy and ache. At times I know before the meteorologists know. I feel clumsy on those days and everything takes more effort. After winter, a period of relief usually follows, but this was not the case this year.

Winter came to an end earlier this year, but the symptoms remained and never dissipated. The only difference was varying degrees of intensity, but the nagging pain remained. Life changed for me at a faster pace this year. I was reevaluating my truths and everything I have come to know in my journey. Not really a bad thing and again I realize that it was adversity and pain that stretched me into my higher self as a person. I now recognize those patterns and by knowing that the outcome is always something beautiful and greater if you carry hope and belief within your heart, I have learned to embrace the pain. But I also learned to understand how someone becomes depressed or gives up all together, not wanting, or unable to face another day filled with pain, be it physical or psychological. It was difficult to function and even more difficult to make it through a day at work. Minutes turned into hours of agonizing pain and even hiking became a challenge for longer distances. I didn’t trust myself and my footing was unstable and frail on the trail. I had no choice and requested a referral to a rheumatologist. After a few troubles and denials, I was finally accepted by a local praxis. Yippie…right, but now is probably a good time to remind you that I have little belief and faith in doctors these days and that my first rheumatologist placed me on cancer medicine without my knowledge, that depleted almost all of my white blood cell count. A common could have killed me without me knowing it. Needless to say I never went back and have been on my own ever since, going through life with a chronic illness untreated.

My September trip to Germany was around the corner and I was in so much pain. I had no idea of how to make the strenuous journey, handle the luggage and the stress of the trip without triggering an even bigger flare. I had to take charge and off to the new doctor I went just before the trip. I saw a nurse practitioner and I liked her a lot. She took the time, she listened and still had a genuine desire to help vs. being consumed by pharmacy kick back of prescribing pills and seeing her patients as a number and dollar sign. She wanted to be sure of what she was dealing with and a barrage of blood tests in the excess of over 1000.00 dollars was ordered. In addition there were X-Rays of my hands and wrists. I told her of my fear of the upcoming trip and she offered steroids I could take as needed in order to have some quality of life, manage the stresses of the trip and be able to function while in Germany. I knew I had no choice, despite my pill dislike and later that day I filled a prescription for Prednisone. Over the next few days it would diminish the edge of the pain, making it tolerable and I left for Germany. Prior to leaving, we scheduled a follow up appointment to go over the blood work and the X-Rays. I wondered about the results while I was in Germany and I knew it was time to face the truth. I was wondering if RA was the only info she would confirm or if a truth would follow that I wasn’t even aware of yet. I tried not to think of it too much and I surrendered. It was out of my hands and I had to be ok with whatever was coming my way. If I needed to believe more than ever, then now was the time to do so. Regardless of the news, it would be from there that a treatment plan would follow, where a decision might be required, where I find out where the path was leading and where I discover what was on the other of the hill that I was clawing my way up to.

Author:

We are the co-creators of our life and the time is now. More than ever are we needed to support Mother Earth and each other. Together we discover and explore our unique gifts in times of strengths, in times we lean on each other, and in times when we learn from each other. This blog started as an outlet and what I ultimately called my “Warriors Journey.” It was a way to document the ups and downs of my life, sharing my hardships as well as my successes. It showcased the struggles, but more important the ways of how to overcome them. Although we are warriors each and every day, I realized that having to be a warrior, comes from a place of pain. I decided to rename this blog, and “Phoenix Rising” now stands for the story of overcoming such a painful place. My motivation for this blog hasn’t changed and I hope to share inspiration and hope, to create a sense of belonging, a space of being heard, and connecting with like minded beings who instill a sense of oneness. We are never alone, and we are unstoppable in the pursuit of what sets our soul on fire. Who I am in a nutshell... 
I am an energy healer and Reiki Master. I am surviving a chronic disease that I’ve sent into remission three times since my initial bout, 15 years ago. I continuously challenge the status quo and by doing so I change my stars. I am a believer that anything is possible. I am a hopeless romantic and I believe that true love exists on various levels. I am an optimist that will always see the glass as half full. I am a dreamer, believing in endless possibilities. Not even the sky is the limit. I have jumped off of the hamster wheel, and I am writing a new chapter. I am chasing my Nirvana to support my most authentic self. This is my story, I am that Phoenix and I am rising from the ashes. Namaste 🙏🏼💙🦋

37 thoughts on “A future in the balance

  1. Arthritis is no fun, I know. How are you feeling now? Did you get new answers, as we will read about in a following post? You made me curious, Rhapsody.
    I’m awaiting to see a new Rheumatologist too and I do have some knowledge, but nothing about, what is going to happen in short time.
    We need to embrace every day and be thankful to get the day and maybe also to our body for the days, when they are working well.

    Liked by 3 people

    1. Mmmmh yeah you knew, there will be the follow up post about the results and what is going on. Sorry to leave everyone hanging, just wanted to break it down and didn’t have enough time to write it all. Hope to finish tonight for a scheduled post tomorrow. It might have two more parts to it and I hope it might bring you some insight. Everybody is different and ultimately we have to decide for ourselves what treatment is best. Best wishes as always to you my dear friend. Hugs

      Liked by 3 people

    2. Thank you, Irene, for your care and comment here. 🙂

      RhapsodyBoheme, would you consider stem cell therapy and/or gene therapy if either or both were to become available in the future to treat or cure arthritis?

      Liked by 2 people

      1. I wouldn’t say no but of course would need more research to understand the pros and cons. I still feel that there are things I need to do such as lifestyle changes that deem helpful and worthy. Interesting question for sure to consider.

        Liked by 1 person

  2. You always have the most amazing attitude, regardless of your situation! You are a strong woman that can handle anything! Sending hugs and naughty fairies your way!

    Liked by 2 people

  3. My mum has Arthritis and I think she need to give this a read. She always brushes it off, I know she’s in pain. I think she’d benefit from seeing a specialist too.

    Liked by 2 people

    1. Hi Ella, what type of arthritis does your Mum have? The symptoms and treatment can be different from person to person and a one does not fit all. I’m fixing to write two more installments to my topic and share what I decided. Stay tuned and best wishes my dear. It’s an ugly disease.

      Liked by 2 people

      1. I think it’s Rheumatoid Arthritis, I’m not too sure. I know my grandad I never met had the condition. Her hands have been really affected because she’s done a lot of DIY over the years. It’s age related I think.

        Liked by 2 people

      2. If it’s rheumatoid arthritis then it is an autoimmune disorder and her immune system is attacking her joints. It’s a different form of arthritis and this one is not age related. Best wishes for your Mom and many painfree moments. Hugs

        Liked by 1 person

      3. I think it is different from that. Like I said my mum doesn’t really tallk about it with me. Thank you very much, wishing you all the best on your journey too, glad I can follow it!

        Liked by 1 person

  4. I have several friends with arthritis, not RA however. I taught immunology for 10 years and have followed the research-there is so much more they need to know about this AID. Sorry you have to bear this!! Hope you are doing well right now 🙂

    Liked by 2 people

    1. I believe you hit the nail on the head and there is so much left to research. I feel like an experiment each time and I just can’t get over the side affects of the current treatments. Giving up one to fix the other is just not a good enough option for me and I might as well not bother at all as long as I can somewhat function.

      Liked by 1 person

  5. I can’t even imagine what that must be like. I wish I could take the pain away. I know one thing for sure. If anyone could possibly bring balance to a horrible situation, it is you. You have the ability to cherish the days when the pain isn’t quite as bad. Not many people in your shoes could do that. You have many other attributes that allow you to live life to the fullest. Those are a lot of words to say that you are one special woman! 🐉 ❤️ 🐉 ❤️ 🐉

    Liked by 1 person

    1. Thank you so much for your kind word dear Dragon Keeper. You leave me speechless and I’m touched. It’s tough at times and not all days are created equal for me, but like you said you learn to balance it and try to make the best out of it. And as far as being a special woman, well I would tell you that it takes one to know one and you are extraordinary my dear. Much love to you and a special hug. Xo 💙🦋

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