When I was diagnosed with Rheumatoid Arthritis, I didn’t know my life would change the way that it has, still there was so much more about this disease that I just did not know. Each day that I suffer, I learn just a little bit more but never learning all that there is to know about a disease that needs more light shown on it in order to make better progress for those of us who has to live this life.
I didn’t know by having this disease my life would be turned upside down so fast
I didn’t know pain could be as bad as it is with a disease that can be unseen
I didn’t know I would watch that pain make me struggle just to take a few steps, wring my hands or even bend my knees
I didn’t know there was this thing called fatigue that would plague me no matter what I did to fight it
I didn’t know there would be days I would cry for relief from that fatigue and the sleep I need to help me along my days
I didn’t know that slowly my abilities would slip away one by one
I didn’t know how hard it would be adjusting to losing those abilities that I was able to do for so long
I didn’t know with Rheumatoid Arthritis came a barrage of different medications
I didn’t know how hard it would be finding the one that would work best for me or how hard it would be adjusting to them
I didn’t know what is working for me would also make me sick, confused and afraid
I didn’t know I would experience things that made me afraid for myself
I didn’t know I would have to learn to cope with the confusion in my head
I didn’t know all of this would become a part of my normal
I didn’t know learning to cope with it all would take every ounce of strength that I have
I didn’t know this disease would tear at the very fiber of what family means
I didn’t know I would almost lose myself while seeking the support and understanding that would help me to keep going
I didn’t know I would lay my head down wishing to look up into eyes of comfort
Above all, I didn’t know with all that I suffer, many would still walk away from me believing I am not as sick as I am.
What I do know about Rheumatoid Arthritis, it is debilitating, disabling and so misunderstood. So as I continue my journey, I will pray that comfort will come to me and all that suffer from what has become our life altering way.
From All of Us!!
Be Blessed
photo credit: alexasfotos/pixabay.com
June 8, 2017 at 3:22 pm
I got a triple whammy. SLE, RA and osteoporosis. My body is slowly breaking down with organ involvement. Some of the meds are as bad as the problem. Diagnosed in my 20’s, 62 now. I just want to rest…
June 8, 2017 at 7:40 pm
Linda I’m so sorry that you’re suffering. I truly wish you the best. God Bless you.
June 10, 2017 at 8:54 pm
You brilliantly outline the path of my own pain, sadness and fear. You are a gifted writer! Thank you for telling the story of life with RA.
June 10, 2017 at 9:30 pm
Wow Kimberly how sweet. Thank you for reading my blog and it is for all of us. In every word I write it touches someone in one way or the other. I wish you the best and God Bless you.
June 11, 2017 at 10:37 am
My hubby now has pulmonary fibrosis due to his ra his life has now been cut short. Lung function at 44 per cent . He is only 52
June 11, 2017 at 11:50 am
Good morning Jane and Happy Sunday to you and your hubby. I’m so sorry to hear about your husband. It is true many do not know just how dangerous this disease is to us. The effects are horrible and our fight is relentless. I wish him the best through this tough journey. May God Bless you and him and your family. Thank you for reading my blog.
June 11, 2017 at 2:18 pm
Brings tears to my eyes…. Thank you for sharing! May The Good Lord continue to Bless you immensely!
June 11, 2017 at 4:35 pm
Thank you David and I pray the same for you as well.
July 8, 2017 at 9:44 pm
I have OA and RA in my neck, back and hands. I need surgery on my right thumb joint and been getting injections in my spine. This a dreadful disease. I have a blog on this site too documenting my journey with arthritis and my daily challenges. Hope you get a moment to read what I wrote.
July 9, 2017 at 5:00 am
I’m sorry for your tough time and I hope it gets better along the way. Thanks for reading my blog and I will check out yours.
September 19, 2017 at 4:12 pm
I’m here for my sister.
I’m here because she’s in pain and I need to learn more about this disease -not from the internet but- from someone else who’s also experiencing it.
I’m here for my sister because I love her and I need to help her through this as much as I can.
I thank you so much for being here. Because this blog is needed more than you will ever know.
September 19, 2017 at 8:16 pm
It is wonderful that you are there for your sister because for so many of is this disease may be invisible so people don’t think you’re sick. The truth is each and every day we endure pain so you understanding and supporting your sister will help in ways you can’t imagine. I wish her the best. Blessings.
September 30, 2017 at 12:37 pm
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