Mel's story of getting an axial SpA diagnosis (Act on axial SpA)
Вставка
- Опубліковано 24 лис 2021
- Meet Mel, who lives with axial SpA. She waited 14 years to find out the reason she was in so much pain and constantly felt exhausted.
In this video she talks to comedian Sunil Patel about waiting too long for a diagnosis and how, with the right treatment and care, she can be the mum she wants to be.
Whether or not you are under 40, experiencing persistent back pain that wakes you in the night and eases with exercise, check out our axial SpA symptom checker - www.actonaxialspa.com/for-the...
1 in 200 people live with axial SpA.
Do you have unexplained back pain that could be Axial SpA? Let us know in the comments 👇or check your symptoms using our simple symptom checker: www.actonaxialspa.com/symptom...
Enjoying this video? Subscribe! → / nasscentral
We are the National Axial Spondyloarthritis Society (NASS) and we are here to transform the diagnosis and care of people living with axial SpA.
Axial SpA works silently. We don’t.
FOLLOW US ↓
• Facebook / nationalaxialspondyloa...
• Twitter / nassexercise
• Instagram / nass_exercise
• LinkedIn / national-axial-spondyl...
• TikTok / nass_charity
JOIN OUR COMMUNITY ↓
• Receive our monthly e-newsletter nass.co.uk/newsletter/
• Become a member nass.co.uk/get-involved/becom...
• Join a Your SpAce online meetup bit.ly/3WbPCH4
• Find your local NASS Branch nass.co.uk/managing-my-as/in-...
USEFUL RESOURCES ↓
• Contact the NASS Helpline for support nass.co.uk/contact-us/
Find out more at www.actonaxialspa.com
Check your symptoms: www.actonaxialspa.com/symptom...
#ActOnAxialSpA #ankylosingspondylitis
Campaign funded by UCB
It took me over 20 years to get a diagnosis and I worked in the medical field....
I also had my symptoms disappear while pregnant!
What was the name of the medication that she uses? Since there are several Biologics and treatments for it, I would like to know which one she was using so I could also look into it
Hi, while I cannot give the details of Mel's medication given the personal details of that. The group of medicines referred to are Anti-TNF biologic medication. You can read more about these here: nass.co.uk/managing-my-as/medication/biologic-therapy/
We also have help for making medication decisions here: nass.co.uk/about-as/your-space/medication/
It would help to know the name of her medication please
Hi, while I cannot give the details of Mel's medication given the personal details of that. The group of medicines referred to are Anti-TNF biologic medication. You can read more about these here: nass.co.uk/managing-my-as/medication/biologic-therapy/
We also have help for making medication decisions here: nass.co.uk/about-as/your-space/medication/
Does this affect the EYES?
About a quarter of people with axial SpA will have an episode of an eye condition called uveitis at some point in their lives. We have some more info here: nass.co.uk/about-as/what-is-as/your-eyes/
Yes! Absolutely. I would get recurrent uveitis/conjunctivitis in my 20s.
I have had a diagnosis letter very little info but it’s saying spondyloarthropathy is this the same I’m so confused. I get lower back pain. Also I have got sacroiliitis inflammation and I get pain in my shoulders arms hands and ribs but no swelling also taken years for my diagnosis any info would be really appreciated
Does methotrexate help this condition?
Hi, generally methotrexate doesn't help axial SpA. We have more information on the medication available here: nass.co.uk/managing-my-as/medication/ ~Zoë
I wish I could see a rheumatologist and start on medication.
Biologic medications are amazing, changed my life is not an understatement
You dont say what medicației helped......