Email a copy of 'Interview with a young woman living with Rheumatoid Arthritis, Part 1' to a friend
Loading ...
E-Mail 'Interview with a young woman living with Rheumatoid Arthritis, Part 1' To A Friend
Loading ... Loading ...22 thoughts on “Interview with a young woman living with Rheumatoid Arthritis, Part 1”
Comments are closed.
wow- same ole story passing again.. different person.. it’s so sad.. sucks… that damage she got could possibly not have occured if there had been early diagnosis and intervention.
i still can’t let go of the fact that she STILL has JRA as an adult.. it’s not RA it.s JRA.. and she has a blog calling it RA when its not.. this is just a very basic thing that makes a big difference with the diseases yet people, including rheumatologist perpetuate this common practice making it harder for awareness as well as understanding of the prognosis differences etc….
just the same, she is adorable in that picture and I look forward to learning/reading more.
Issadora,
I’m planning to address RA versus JRA on Wednesday, I think, when I am finished with Pamela’s interview.
In the meantime, I’ll just say that I have admiration for Pamela and her recent decision to blog about her RA / JRA and I’m hoping she receives lots of support. O:-)
And this “not getting diagnosed” for so long baffles me because these aren’t just general practitioners. These are the rheumatologists. They should be well aware that one can have negative lab work and still have RA.
My GP diagnosed me on the basis of my hands and feet and because prednisone helped so much. The rhemy agreed although my blood work is neg. I was the one that was most surprised about my dx. 🙂 so every day, my body reminds me. 🙂 I am very thankful for my GP!
Hey kmom,
This is only the second time I’ve heard of a doctor actually trying this method: See what the prednisone does to the symptoms.
I’m amazed: I have suggested that tactic as a diagnosis tool, but only in theory. I’m so glad it worked for you to get an answer. I wonder whether more doctors are trying that. :teeth:
Frustrating indeed. But glad that she was finally diagnosed.
My Rheumy mentioned that a positive reaction to prednisone was also part of the confirmation of RA induced inflammation.
I hate that anyone has to endure this disease, but it hurts me to see kids with it. I was diagnosed with it at age 45. I’m ok with that, I lived most of my life before being diagnosed with it, but I couldn’t imagine having to go through high school, college and your early adult life with either RA or JRA.
I agree with kmom, these were rheumatologists. Why would they just pass her off as having growing pains or muscles were too firm? These are our specialist that we rely on to help us.
Tharr, I so agree with you. I cannot imagine how different my life would have been had I been diagnosed at Pamela’s age. My prayers go out for you, Pamela, that in ten years time there will be even more new meds for you and that this will all be a thing of the past for you.
Noelle
Morning Inspiration,,,,,, THANKS KELLY…This was …
Very touching story, I hope Pamela could face her condition with God’s loving care..
I feel so bad for this young lady, here we always say how devastatied we are that we have RA, but when it comes to one so young, I dont know how I could have gone through my teen years with RA….. and Kelly I was on prednisone most of my youth, it was all they had back in the 60s for asthma… go figure, one med that can help so many has so many ill effects
I hope my daughter is as strong as Pamela is.
Jordan was diagnosed almost 5 years at the age of 3. Part of me thinks that the younger you are when you are diagnosed the better. You don’t know/remember what life was like before. All these meds, appts, tests and so on are routine for J. Me being 35 and just diagnosed has sent me a spin. I’m having a hard time adapting to everything and I find myself having to look to my 7 year old for support.
Pamela’s story sounds similar to mine except I was diagnosed at 23 and had been having symptoms since High School…I’ll be praying for her.
I think one of the oddest things about it is that so many people with RA do seem to be either younger or older; being in the teens or early twenties seems to be a bit of a no mans land. I don’t know if that is just my perception based on sitting in my doctor’s waiting room for too long but…for what its worth.
My daughter was diagnosed at fifteen with RA. She will turn eighteen this month. Her arthritis is the adult version and I am humbled everyday to watch her live her life coping with this unpredictable disease. I am amazed at her bravery, and desire to live her life the best she can with the cards she has been dealt. Her faith sustains her and frankly she has been much braver than I have. Good luck Pamela.
Jane,
We have several young people who comment on the blog, so I don’t know if I’ve ever spoken with your daughter. Please give her a hug for me. The only thing I can imagine harder than living with RA would be to be a young person living with RA.
Thanks for being the wonderful kind of mom who would read a page like this. So many with RA have families who don’t understand at all or ever read something like this story so they will. She’s lucky to have you. God bless you both. :heart:
I am 18 and was diagnosed with RA two years ago. I just discovered this website/blog, and I have been looking for other people my age with RA; I have never talked to anyone my age who has it. Living with this in college is hard, and I would love to connect with someone who shares my age, health situation, and faith! Do you know if Pamela has a blog anymore? Anyway, thank you for blogging about this!
Hi Allison. I’m glad you found us! It must be so hard for you. I have daughters your age & I can imagine! Bless your heart! :heart:
There are a number of girls your age I hear from here on the blog sometimes. If you see a comment from one of them, go ahead & reply. If they don’t see it, I could email them to see if they want to get in touch. Let me know if you want me to try that.
Pam has moved her blog. I’ll fix the link! She is also very active on Twitter so if you’d like to try Twitter, you could follow her & me there & we could help you find friends. Click here for Pam’s blog link. Click here for Pam’s Twitter link. Click here for my Twitter link.
thank you for sharing this! I was diagnosed with JRA when I was 14. It is now 7 years later. I enjoy reading stories of other young women my age.
I was diagnosed with Juvenile Systemic Arthritis in 1993. I was only 16. I have suffered through the severe pains of inflammation through out my body. I also have uveitis.
I have a new Rheumatologist who doesn’t think I should call my condition JA because I am now 35. He said, JA can become RA or AS or simply stay as Still’s Disease (JRA) or go away
Hi Pricilla, Rheumatologists differ a lot on this. I guess as long as you get good care and treatment, it doesn’t matter much what their perspective is. It does matter for research and we may advocate a more holistic view in the future. And it matters to the majority of families who are told that the children will outgrow it and then do not – so it will of course be good to know more and have better data about kids who get this disease and their outcomes.
More answers to questions I have had. My heart breaks for this young lady in not being diagnosed. Hear from more and more people that have negative blood tests but do have RA. My prayers are with her as with all of us who suffer from this disease.
God Bless You Kelly.
Dear Kelly,
I am a middle school student in Singapore and have recently been set the task for my Design Technology project,
In order to complete it I would need to interview a person with arthritis,
I was just wondering would you by any chance help me with this project so I can interview you?
All the best
sent you an email Eliza