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Photo testimonial: Maintain hope despite the side effects of treatments for rheumatoid arthritis

Published 19 Mar 2019 • By Louise Bollecker

"No one warns you of the side effects: hair loss, nausea... Cortisone reduces inflammation and makes pain bearable but it gives you something extra: hello weight gain."
Photo testimonial: Maintain hope despite the side effects of treatments for rheumatoid arthritis

 

Virginia's testimonial
Maintain hope despite the side effects of treatments for rheumatoid arthritis

 

rheumatoid arthritis

Shortly after the birth of my third child, I started to experience joint pain. I was told that this was normal after childbirth, in addition to having three children to manage, a home and a job. After several discussions with my physician and a battery of tests, the verdict fell: "Madam, you have rheumatoid arthritis".

The hope of the diagnosis

Magnificent, I could finally put a name to this invisible disease and which, therefore, is not understood by those around me because the pain is not visible. The treatments followed one after the other to try to reduce this pain but in vain.
One day, my rheumatologist prescribed a so-called biological treatment, what a beautiful word to hide the fact that you are injected every month with a molecule used in oncology. This treatment allows you to move a little more and slow down the progress of this disease.

Side effects of biological treatment

But no one warns you of the side effects: hair loss, nausea... Cortisone reduces inflammation and makes pain bearable but it gives you something extra: hello weight gain. It's hard to see your image change, to admit that physically, I'm diminished. It's hard in the morning when your brain says "let's get up" and your body says "uh... no".
I sometimes feel humiliated and so misunderstood by those around me who do not know this pain, which is very much present day and night.

Maintaining hope despite rheumatoid arthritis

I try to find something positive: a day with bearable pain is a day saved. I try not to get discouraged and keep hope, there are better days.

And during those better days, I try to be a normal mother, a mother who is not in pain and who can do activities with her children even though I know that the next day will be a real pain.

I enjoy every positive moment and I say to myself every day "Carpe Diem".

This testimonial is part of the graduation project of Gaëlle Regnier, a student in photography at the Agnès Varda School of Photography and Visual Techniques in Brussels. She chose chronic pain as the theme of this photo report to highlight the patients and their struggle.

 

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Carenity

avatar Louise Bollecker

Author: Louise Bollecker, Community Manager France

Community Manager of Carenity in France, Louise is also editor-in-chief of the Health Magazine to provide articles, videos and testimonials that focus on patients' experiences and making their voices heard. With a... >> Learn more

3 comments


JosephineO • Community manager
on 19/03/2019

Can you relate to this testimonial? What did you think?

@ellis1949‍ ‍ @Bridget1‍ @MandyG‍ @beagle ‍ @moosue‍ @AlexLoui‍ @proudofthebrave‍ @Annanngriff‍ @Ferdy73‍ @Cazcartoon‍ @BookerBoo‍ @Claireie‍ @Myo3557‍ @raining‍ @marydollathome‍ @cataddict‍ @Trace01‍ @chele23‍ @Sarahbee‍ @Tantagg‍ @tess277‍ @Lorenzonk84‍ @jools_warwick‍ @Cally90‍ @Brumden‍ @Jimjacduffy‍ @Kerry43‍ @Margret‍ @nannakay‍ @Carmelq ‍ @Vic9986‍ @annette‍ @Daisymay‍ @MandyP‍ @CharChar‍ @lynnsky43‍ @Jones123‍ @grannypam‍ @dykes2‍ 


moosue
on 20/03/2019

Hi, yes I relate to a lot said in the above.

I am on a bio drug ,I have noticed minor improvements in the reduction of pain, Due to which  I may be able to reduce the steroids I have been on for 11 years, Through which I have now just been  told I am on the cusp of diabetes and raised cholesterol, After which I’m feeling a bit low but upward and onward.hugs to all.


on 08/04/2019

Yes, I can relate to all of it and am now on my third bio treatment, trying to be positive and active knowing you will pay a price for this is very hard. I can hardly look at myself and do not like how my body has changed due to all the meds. I will carry on until I can no longer. As the lady said Carpe Diem. 

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