The past 6 months have been somewhat like a bad dream. I never could never have imagined being sick for this long with so many different ailments. I can’t help but wonder if all the years on methotrexate had such an effect on my immune system that everything kind of shut down for a while. With all this down time I have had the opportunity to learn somethings about myself. I thought I would share some of what all this sickness has taught me.
- Trust your instincts. When two of my doctors had conflicting opinions on whether or not I had a second or continuing Lyme infection I should have trusted my instincts. I could have saved myself valuable time and pain and not have subjected myself to way too many diagnostic tests had I just trusted my gut. I know my body better than anyone else and I knew that I still had Lyme Disease. I shouldn’t have allowed my rheumatologist to talk me into more tests to prove that her opinion was right when I knew deep down inside all I really needed was another treatment of antibiotics. When I finally got the antibiotics was when the symptoms went away and I started to feel better. Lesson learned. Again. I hope this time it sticks.
- Lyme Disease is something to take very seriously. I have had Lyme Disease in the past. I thought that I knew and understood what this disease could do. I could not have been more wrong. I have never in my entire life felt more physically ill than I did with Lyme Disease. I can’t say whether or not the Rheumatoid Arthritis (RA) had an effect on the severity of the Lyme Disease but I know that the treatments for the RA had an effect on how well my body was able to handle Lyme Disease.
- I need to nourish my body and my soul. I have always been the one who puts everyone’s needs before mine. It wasn’t a conscience decision, but none the less other things took priority in my life. Now every day I am slowing down and taking time to do things that nourish my soul. Things that bring me joy nourish my self. I find that I have more patience and energy for other things after making my self a priority. Before I put anything into my body I am asking myself will it nourish me or fill me. They are two very different ideas. I have tried to eat responsibly in the past, but I haven’t always looked at what I am putting into my body as nourishment as opposed to something that will fill me up.
- Don’t be afraid to ask for help. Being an independent person and a bit of a control freak I frequently would rather do something myself than ask for help. Part of me just didn’t want RA to get the best of me. I felt like it was a bit of a battle of wills. I wasn’t going to let RA take over my life completely, I could do most things myself and I hated to ask anyone for help. Being as sick as I have been, I have had no choice but to ask for help. There were days when getting out of bed to go to the bathroom was an ordeal. An extremely painful ordeal. It was simply impossible not to ask for help with some of the most basic of needs. I discovered that the world did not end and it was okay if things were not done “my way”.
- A clean is nice but really not all that important. I used to care very much about how clean my house was. I felt that how my house looked was a reflection on me and how I cared for my family. I know that sounds a little nutty but that is how I felt. I really felt like I could not physically do a great many things anymore but I could take care of my family and a clean house was part of that. Of course now looking back I can see how crazy that whole idea sounds. My house currently is picked up. No one is going to trip over anything in my house, but it is a far cry from clean and I really don’t care. I could spend the next few hours cleaning, or I could spend the next few hours playing with Kevin or reading a good book. Now I choose something that will fill me up instead of depleting my resources.
- Connecting with other people that know and understand what it’s like to have RA is important. Knowing that I am not alone in the day to day challenges that this disease brings has helped me in so many ways. There is comfort in knowing that there are people out there that completely understand what I am going through. I am very grateful to all the new friends that I have found here and for their kindness and support.
Tags: ailments, antibiotics, arthritis, body, diagnostic test, disease, infection, lyme, lyme disease, methotrexate, nourish, RA, rheumatoid, rheumatoid arthritis, rheumatologist, sick, soul
Excellent post yes with Lyme Disease we do need to take time to get to understand the illness and what our bodies are telling us as well as finding a good Lyme Literate Medical Doctor.
I recently found this website which is worth looking at for anyone with Arthritis or Rheumatism
http://www.roadback.org
Good luck with getting rid of your lyme Disease again.
Thanks Joanne. I will check it out.
I was initially diagnosed with lyme disease before my kidneys gave away my lupus. I am glad things are easing up for you and am sending you a gentle pat on the back…those lessons worth learning need to be reinforced from time to time to keep us humble and paying attention.
Smiles~
So true. Thanks for all your support Maria! It means so much.
Jo-Ann, I read this post thinking, “This is me!”. You described so much of what I also have learned while being sick. I really liked the part about nourishing your soul. That is so important, isn’t it? Also, asking for help was a hard one for me. Even recently I have been asking my husband to help with dinner and thought, “All these years of thinking he should read my mind and just help when I could have just asked and he would have been happy to help.” It is nice working side by side and all I had to do was ask. Seems simple now but so hard before. Thanks for sharing. This is one post I will be back to read again.
Thanks Cathy,
I have done the same thing with dinner. My 15 year old son Nathan for Christmas gave me the gift of him cooking dinner once a week for the year. I wish that I had done this years ago!
Hey Jo-Ann,
I have to admit, this last year has been so crappy. I almost said pure hell, but looking beyond myself and my body I have so much to be happy about and thankful for.
Thank you
I stopped by your blog and read your list. Amen. I need to take some of your advice and apply it-knowing my own bod better than the docs. I can’t tell you how many times I let myself suffer while they tested. And I FINALLY let my house go. lol. I used to be OCD about it, a clean house or dirty, that’s how my mood went. sigh.
You know, I’ve put myself into practical seclusion, and I really do need to talk to people with the same things going on. I might just stop by now and then and bug ya ;0)
I hope that you are feeling better and wishing you pain-free and stress-free days. Getting up in the morning and not feeling the RA, but the ‘old you’. Feels like walking on a cloud! (I think I”m gonna wish it for me too, lol)
Hugs,
Michelle
xo
this comment is copied and pasted from my blog as my response to you hun. sorry, fingers are a hurtin.
I sure hope you are feeling better now. There is alot to be learned when you struggle with serve conditions like RA. I did know how severe lyme disease was. Well, I am glad you have seen and gotten to the light at the end of the tunnel. It sounds like it was scary ordeal. Keep taking care of yourself.
Thanks Lana,
I know that you are having a bit struggle lately with your hands and I hope that it gets resolved soon. One minute in pain is too much.
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