Erika Dawn Hodgson

RA Guy Real Profiles of RA 6 Comments

Real Profiles of Rheumatoid Arthritis
Photos © Erika Dawn Hodgson


Erika Dawn Hodgson




Calgary, Alberta, Canada

How long have you lived with RA?

I was officially diagnosed in January 2010, but have had joint swelling and issues for about 5-6 years.

What advice would you give to someone who has just been diagnosed with RA?

Ask your doctor for potential links to support networks as well. This was something I didn’t do in the beginning. I saw my Rheumatologist, received my diagnosis and then walked out with no information. I did my own research though, so being armed with the education, however you obtain it, is valuable.

Do you use any mobility aids?

When my knees were really really bad I would use a cane. Since medication though, I have had very few problems with the knees. When my elbows were at my worst I used my children as aids…running and getting me things etc…

How has living with RA helped to improve your life?

I am much more grateful for what I have in my life. I feel like I can teach my kids by example, to plod on in life through the difficult moments, because there are ALOT of them. I feel happier and more confident too, because when I started researching RA, I started educating myself about alot of issues and health concerns. I have other autoimmune diseases that are tricky and annoying and that affect my life (for instance, I have alopecia, so I am visibly different to most others) – and the RA has given me the opportunity to focus less on that and the other diseases, because in comparison, they really aren’t that horrible – and none of these things have ruined my life exactly.

Do you have any visible signs of RA?

When I flare my elbows look twice their size and I can’t bend or straighten them. They are big and red and hot and angry looking. The way I walk because of some damage in the knees and ankles is a sign, too.

Can you please describe some of your favorite coping strategies for living with RA?

Talking about my frustrations with people who care and want to listen. Educating myself more. Putting myself out there on message boards and resources like this to show people that life doesn’t have to be awful when you have RA or other diseases. When I accomplish more and more physically during the days too, it makes me feel good about myself, both like I have accomplished something kind of major in my world, but also knowing that I am setting a good example for the kids and my friends and family. I also focus on not feeling guilty on the days when I accomplish nothing but rest. Rest is good though, and needed.

Can you please describe your current medical (traditional and alternative) treatments?

Regular gentle exercise for starters, Methotrexate, Prednisone, Folic Acid, Ibuprofen, Losec and I try to get all my vitamins and calcium through diet because vitamin pills kill my tummy.

Is there anything else about yourself that you would like to share?

I’m a MOM of two first and foremost – my children are who make me want to continue on this path of education, happiness and contentment. I live with RA, Alopecia Areata Universalis, Chronic Uveitis that flares up often, Thyroid disfunction, a bulging disc in my back from years of walking funny and a recently diagnoised pulmonary embolism. Life is too short to focus on all of the negative things, and I say that I live with these disesases and I mean it. I live with them. They don’t run my life, they don’t define who I am, but they are my daily challenge in this life, and you know what? I feel like I am conquering mountains sometimes just by facing the day, and that feels good when I can function and feel contentment.

Comments 6

  1. Steve

    I think having a solid support group is really important and agree that it is something many people don’t even think about. It can be a tremendous help to have others that have a similar situation that you can speak with and get advice from. It is great that you have such a great outlook too, that helps a lot!

  2. Sherri Danyluk

    Thank you so much for sharing this I am part of the support network as I am Erika’s mom. She has taught me alot as well about RA and all of the meds that she takes to function in daily life. I am so proud of her and all the things that she has accomplished as a woman and as a mother. She remains positive and an absolute joy to talk to about any problem that may be plaguing her or any friends or family, or to just chat about days events. Love you dearly.

  3. Moselle

    Erika you are such a beautiful woman! We could all learn from you. I wish you a wonderful, pain free Christmas and New Year.

    Sherri it takes a strong woman to be able to support someone who suffers through chronic illnesses. She is lucky to have you, as are we all.

  4. Erika

    Thanks everyone for the lovely compliments.
    You are right, I am very lucky. I have a good supportive network of friends and family who understand that daily life can be a little more of a hastle to get through than for the average Erika. 🙂 Im proud of be a part of this site!

  5. emma

    I am currently awaiting confirmation of an RA diagnosis. I think you are absolutely amazing. And the comment fromy your mum is BEAUTIFUL! Thank you for inspiring me.

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