Getting My Diagnosis PT3 Chronic Illness Diagnosis Ankylosing Spondylitis

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Hope you are all having the best day with minimal pain!
Thank you for taking the time to watch my videos on my diagnosis story. I really hope you can find comfort and hope from them for yourselves, if you’re going through a similar thing. It may not feel like it now, you are exactly where you need to be in your life, and you’re on the right path. Be as strong as you can, and take each day one by one.Wishing you all a positive week, be kind to yourself and make healthy choices!
Let me know if you liked this video by giving it a thumbs up, this lets me know that you enjoy this type of content and I will make more for you. Remember to subscribe to my channel, I'd love it if you would stick around!
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Part 1 - Blood tests
• Chronic Illness Diagno...
Part 2 - Rheumatologist Appointment
• Rheumatologist Appoint...
Part 3 - Getting my diagnosis
• Getting My Diagnosis P...
Part 4 - Physio
• Physio PT 4 Chronic il...
Part 5 - Starting my medication
• Starting Medication PT...
Part 6 - My autoimmune disease Upgraded Itself
• My Autoimmune Disease ...
My video on tips of how I accepted my chronic illness
• How I Accepted My Chro...
My video about the mental challenges of living with a chronic illness
• The mental challenges ...
Need help with injecting your medication? do it with me!
• Inject Your Medication...
Explaining Ankylosing Spondylitis video
• Ankylosing Spondylitis...
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INTRO / OUTRO / OVERLAYS
Designed & created by Video Editor Em
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[@AnkylosingSpondylitisMan]

Sorry to hear about your diagnosis, the emotional reaction is perfectly understandable. Stay strong!

[@user-hb8lj8lz7h]

❤❤❤❤aww my darling, i live with chronic pain, spinal nerve damage, and spondylitis, im older 62yrs with 2 daughters and grand children, just want to say your young think positiv, there is lots of meds now, god bless you jayne ❤❤ walton, of bristol, love to you❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤

[@286sitar]

Hello
I have recently started medication for my autoimmune disease after months. I was wondering when the normal followups are after the initial rheumatologist appointments.
I have been given a follow up with a nurse in 12 weeks is that normal?
Just trying to figure out the NHS system

[@lavintella]

Hi! I'm watching your videos and they help me a lot not to feel alone struggling to get a diagnosis, your symptoms are very similar to mine and regarding your dizziness, I'm now convinced that it can be related to AS, this other young woman talks who has been diagnosed with AS as well in France, talks about that symptoms that was her main one for a long time (it seemed related to AS affecting a cervical spine), maybe you can unterstand her with the automatic translation (my native language is French so I can understand her) ruclips.net/video/M1WETSyUbBM/видео.htmlsi=4meybOnOMZHWNr1w