Home Actress Jess Impiazzi HD Photos and Wallpapers October 2023 Jess Impiazzi Instagram - A lot has been going on here since the start of the year!… I don’t know where to begin! Obviously I was very open with the IVF journey and the process, but during that time and pretty much since early January I had been getting sicker and sicker, this was with inflammation, stomach issues that were debilitating. As the months rolled on I’d have muscle spasms, my joints would swell and I’d be unable to move my entire body, my eyesight got worse, the fatigue was something and is still something I’ve never experienced before. From being in the gym nearly everyday and running 5k’s this has just been horrid. Then I got rashes all over my chest arms and face (I’ve learnt how to cover them well with make up, but without it it’s horrible down my nose and my whole forehead) In July I had three trips to A&E from the pain, I just knew I was getting worse and I was really struggling! Mentally it’s taken a toll, if the IVF and that failing wasn’t hard enough this was topping it off! After many, many tests and lots of blood taken I was diagnosed with a chronic autoimmune disease called Lupus. (Swipe along to see more info on lupus taken from @lupus_uk) I am currently on steroids to get this under control and then see what the future holds medication wise but having a diagnosis helps as I can now work with the doctors to get myself living again and do whatever it takes to keep my body in the best working condition! I’ve had amazing friends and family supporting me! (You know who you are!) I’m looking in to something’s as to why it’s happened and what may have caused it although it’s hard for doctors to establish that, however I did have an operation late December last year that I feel may be linked. (I’ll talk about this in detail once I know more) If anyone has autoimmune issues especially lupus please reach out and let me know ways that may have helped you! Anyways… that’s what’s been going on lately and have felt a little bit lost but I’m finding my feet again! I’ll bounce back with tweaks and get the show back on the road! 🌈🦋💖 peace and love to everyone 💖🎀🦋 a thank you to @susehilly for helping me tell my story in todays paper 💖. #lupus #autoimmune #ivf

Jess Impiazzi Instagram – A lot has been going on here since the start of the year!… I don’t know where to begin! Obviously I was very open with the IVF journey and the process, but during that time and pretty much since early January I had been getting sicker and sicker, this was with inflammation, stomach issues that were debilitating. As the months rolled on I’d have muscle spasms, my joints would swell and I’d be unable to move my entire body, my eyesight got worse, the fatigue was something and is still something I’ve never experienced before. From being in the gym nearly everyday and running 5k’s this has just been horrid. Then I got rashes all over my chest arms and face (I’ve learnt how to cover them well with make up, but without it it’s horrible down my nose and my whole forehead) In July I had three trips to A&E from the pain, I just knew I was getting worse and I was really struggling! Mentally it’s taken a toll, if the IVF and that failing wasn’t hard enough this was topping it off! After many, many tests and lots of blood taken I was diagnosed with a chronic autoimmune disease called Lupus. (Swipe along to see more info on lupus taken from @lupus_uk) I am currently on steroids to get this under control and then see what the future holds medication wise but having a diagnosis helps as I can now work with the doctors to get myself living again and do whatever it takes to keep my body in the best working condition! I’ve had amazing friends and family supporting me! (You know who you are!) I’m looking in to something’s as to why it’s happened and what may have caused it although it’s hard for doctors to establish that, however I did have an operation late December last year that I feel may be linked. (I’ll talk about this in detail once I know more) If anyone has autoimmune issues especially lupus please reach out and let me know ways that may have helped you! Anyways… that’s what’s been going on lately and have felt a little bit lost but I’m finding my feet again! I’ll bounce back with tweaks and get the show back on the road! 🌈🦋💖 peace and love to everyone 💖🎀🦋 a thank you to @susehilly for helping me tell my story in todays paper 💖. #lupus #autoimmune #ivf

Jess Impiazzi Instagram - A lot has been going on here since the start of the year!… I don’t know where to begin! Obviously I was very open with the IVF journey and the process, but during that time and pretty much since early January I had been getting sicker and sicker, this was with inflammation, stomach issues that were debilitating. As the months rolled on I’d have muscle spasms, my joints would swell and I’d be unable to move my entire body, my eyesight got worse, the fatigue was something and is still something I’ve never experienced before. From being in the gym nearly everyday and running 5k’s this has just been horrid. Then I got rashes all over my chest arms and face (I’ve learnt how to cover them well with make up, but without it it’s horrible down my nose and my whole forehead) In July I had three trips to A&E from the pain, I just knew I was getting worse and I was really struggling! Mentally it’s taken a toll, if the IVF and that failing wasn’t hard enough this was topping it off! After many, many tests and lots of blood taken I was diagnosed with a chronic autoimmune disease called Lupus. (Swipe along to see more info on lupus taken from @lupus_uk) I am currently on steroids to get this under control and then see what the future holds medication wise but having a diagnosis helps as I can now work with the doctors to get myself living again and do whatever it takes to keep my body in the best working condition! I’ve had amazing friends and family supporting me! (You know who you are!) I’m looking in to something’s as to why it’s happened and what may have caused it although it’s hard for doctors to establish that, however I did have an operation late December last year that I feel may be linked. (I’ll talk about this in detail once I know more) If anyone has autoimmune issues especially lupus please reach out and let me know ways that may have helped you! Anyways… that’s what’s been going on lately and have felt a little bit lost but I’m finding my feet again! I’ll bounce back with tweaks and get the show back on the road! 🌈🦋💖 peace and love to everyone 💖🎀🦋 a thank you to @susehilly for helping me tell my story in todays paper 💖. #lupus #autoimmune #ivf

Jess Impiazzi Instagram – A lot has been going on here since the start of the year!… I don’t know where to begin!
Obviously I was very open with the IVF journey and the process, but during that time and pretty much since early January I had been getting sicker and sicker, this was with inflammation, stomach issues that were debilitating. As the months rolled on I’d have muscle spasms, my joints would swell and I’d be unable to move my entire body, my eyesight got worse, the fatigue was something and is still something I’ve never experienced before. From being in the gym nearly everyday and running 5k’s this has just been horrid. Then I got rashes all over my chest arms and face (I’ve learnt how to cover them well with make up, but without it it’s horrible down my nose and my whole forehead)
In July I had three trips to A&E from the pain, I just knew I was getting worse and I was really struggling! Mentally it’s taken a toll, if the IVF and that failing wasn’t hard enough this was topping it off!
After many, many tests and lots of blood taken I was diagnosed with a chronic autoimmune disease called Lupus. (Swipe along to see more info on lupus taken from @lupus_uk) I am currently on steroids to get this under control and then see what the future holds medication wise but having a diagnosis helps as I can now work with the doctors to get myself living again and do whatever it takes to keep my body in the best working condition!
I’ve had amazing friends and family supporting me! (You know who you are!) I’m looking in to something’s as to why it’s happened and what may have caused it although it’s hard for doctors to establish that, however I did have an operation late December last year that I feel may be linked. (I’ll talk about this in detail once I know more)
If anyone has autoimmune issues especially lupus please reach out and let me know ways that may have helped you!
Anyways… that’s what’s been going on lately and have felt a little bit lost but I’m finding my feet again! I’ll bounce back with tweaks and get the show back on the road! 🌈🦋💖 peace and love to everyone 💖🎀🦋 a thank you to @susehilly for helping me tell my story in todays paper 💖.
#lupus #autoimmune #ivf | Posted on 17/Sep/2023 14:06:46

Jess Impiazzi Instagram – A little Lupus update!

For the last few weeks I’ve been on a lower steroid dose (5mg a day of prednisone) and 300mg a day of Hydroxychloroquine. The new medication (hydroxychloroquine) has started to really work and I’m feeling a lot more like myself. 
Im still nowhere near the old me yet, but I’ve managed a couple of light yoga classes and that’s been great.
I get pain in my spine which is sore but nothing like I was a few months ago where I couldn’t get out of bed.
I have a consultation tomorrow with a surgeon regarding removal of breast implants. I’ve done a lot of research and these implants in the body can cause autoimmune triggers in some people (quite a lot of people I’ve found out) my last implants ruptured early last year and I had minor fatigue and some weird blood results but nothing was done as it was nothing serious. When I had them removed and replaced in December last year it was two weeks until I started getting extremely unwell. It started with gastrointestinal issues and then my hormonal system and so on until I was diagnosed with an autoimmune disease. So I’ll be speaking with my surgeon tomorrow to get them out asap as it’s very coincidental timing. 
However, although I feel physically better I’m still getting brain fog albeit not as severe but my hair is also thinning, falling out a lot daily and that’s causing me a lot of worry.
Fingers crossed removing the implants can help clear some of these symptoms up. Time will only tell on that front.
For now I’m taking the positives, I’ve been really strict on my diet and meditation to remove any stress as all these things help the body alongside my medication and I’m also taking tumeric supplements to help with inflammation. 
So I’ll keep enjoying the good days and keep everyone updated as things happen.
I’m very interested to learn as much as I can about implants in the body and I watched #thebleedingedge on @netflix which was quite the eye opener! 
If anyone has similar stories with their health I’d love to hear from you #lupus #autoimmune #implants #bii
Jess Impiazzi Instagram – ‘If you want to see the sunshine, you have to weather the storm’ 🌈🦋