After 6 years of chronic pain and inflammation, thyroid, fractures, muscle spasms, asthma and many more, one day your left index PIP (Proximal Inter Phalange) joint swells and doesn’t move (ain’t pretty). You think ah! been there done that, might just be another break but surprise surprise! (not a good one clearly). Worried me went to an orthopaedic doctor who recommended a surgery. Now worried and scared me(because I had a surgery in just December) reached out to my cousin for his opinion who knows my long medical history. This cousin is the one who recommended, 4 years back when he visited India, to go to a rheumatologist as he felt something was missing in my diagnosis. But unfortunately, that rheumatologist didn’t diagnose properly. Now as one more symptom has come into light my cousin recommended all possible x-rays, blood works and combined with hours of consultation with his friend the answer was revealed – “Autoimmune Arthritis”
“Arthritis?! How old are you?” you might ask. Well just going to be 30 (this October) but my body behaves like its 60 years and my heart thinks its still stuck at 3 years! I was going through mixed emotions. I was in great pain and it made me think of others who are experiencing similar issues with no proper diagnosis pained me more. Especially when it comes to women there is a long history of dismissing pain. We don’t know if this is implicit bias or the way we judge women and pain in terms of their presentation for clinical conditions. The history of downplaying symptoms told by women is ridiculous and awareness should be raised around this.
But along with pain I was also happy that I finally got the proper diagnosis and a bunch of people as my support system – my husband, my parents, my in-laws, extended families and dear friends. And two people in particular, my cousin and his friend who made sure to monitor my symptoms and evaluate the reports everyday for 2 weeks. I felt blessed and grateful but this also made me sad about my condition and that I have to be on medication for next few years or maybe for life. Told you right? Mixed emotions! I am OK though.
From this experience of going to hospitals numerous times for tests and consultations now at these scary Covid-19 times made me realize how hard it is for young parents like my brother and me who can’t stay away from their kids. My kid and my brother’s kid would be waiting to hug us a soon as we come from hospital but had to beg them to stay away (which they don’t understand why) until we sanitize ourselves. Its heart wrenching to keep them away even for that little period of time and its frightening as to what we are bringing home to our kids and family from those visits. Words can’t express what I felt for how my brother and Sudhir who supported me and accompanied me in all these visits (Love you both!!!). Extremely thankful and grateful to my parents and sister in-law who were very supportive. My heart goes to all those people who are facing the similar situation and hope they all stay safe & healthy.
Now that I know the problem (Arthritis) I can work towards the solution. I’ve always been strong and that helped me put a smile on my face even under these circumstances. But what to do with comments like “you look healthy, chubby and fat, what’s wrong with you?” (which have become part of everyday conversation)??? Here is my answer – How I look isn’t an indicator of my pain. You don’t have to approve it, accept it, understand it or even acknowledge it unless you’ve x-ray eyes to see my periarticular osteopenia. I hope one day we get to live in a society where we’ll have no one judging others by their looks. These people could be in physical or mental pain, may be a heartbreak. We don’t know the story so we don’t have the right to judge. Let’s be kind to one and another if we can or keep it shut. Period.
















