I'm most happy when I'm plucking weeds in my gardens. I'm a sun worshiper. I've had psoriasis since I was born and usually it's mild unless stressed.
Its my fault in some way for researching into mesh hurnia repairs but is it? NOOOO not really as i was told its safe and i knew people no problems with mesh implants , Not until things go wrong then you do research like i did , though for over 2 years i thought it was something else and docs never said a word to me about this,. I have ranted at Docs about it but they like to dismiss the mesh even though there thousands in the uk whom have problems, I weould had rather left it as it was tiny and not painful at all unless i coughed but otherwise it was okay,Thought best get fixed while its small,surgeon didnt say i could have a host of problems and docs never picked up on it .One doc just said, your not the only one lol, What a thing to say? unbelievable really. Now its going to cost more money for them and some from me to try help me like thousands of others, so they shouldnt be using mesh, Woman can get destroyed too with mesh, Someways i think we are in the dark ages to be happy to gamble and put a lot of people through torture. I spoke to many people whom had Auto immune response from mesh , basically rejection, I have accepted what is as i have to. Luckily i can still walk at the moment and i hope i still can ,People out there in worse situation than me Thanks :)
Keep it together John, pain sucks, enstilar is for skin, it sucked for me lol, so that's it, done. Psrioasis is not so bad even all over, till you deal with with oa, /psrioasis /psrioatic arthritis, it's, a, diff life and you want to die, but you don't so you are here. That's how I deal, cheers and you will find a way
Thank you Rosey, Well ihad psoriatic arthritis since 2003 but never had an onset like it was this time,My diet/lifestyle kept it near none existant for over 3 years and then just went nuts, I had been feeling fluey for sometime so it was working up to it, Once that mesh really sinking into my inners and pain started in places that wasnt there then that was it,Believe me though , if you stick to eating mainly veg .chicken and fish , steer clear of dairy , sugar eat fruit or have rarely then withing 5 months your be ammazed how much you may reduce symptoms or clear it to near gone,I have evidence of inflammation that was left behind, nodules on my wrist and thumb, didnt have any problems until now,It does take effort and my skin is got mind of its own but , If you leave these things you end up more pain and nodules,Its all a choice though i know and not easy, like you my skin dosnt make a difference but i rather have dodgy skin than painful crippled joints given the choice,My symptoms have calmed down as now i am to stage 2, Fever and it getting in joints last week now its going start try and destroy my joints , I am eating well and hope i can get this back as it was to nothing but maybe difficult because of this mesh that caused me get like this . I wish you well Rosey :)
I jnow Rosey but i like makes sure i got all the nuitriance i need ,Yes my psoriasi dosnt make any difference, lifestyle does to my joints, well it did with psoriatic arthritis , Thank you Rosey, still rough as hell, i got try to work, will i make it lol, No docs cant help you unless you need meds thats it, never cure you or anything Thanks
It means everything to have such wonderful support, especially in hard times. Here in Canada the government is saying there will be support for workers, some banks are deferring mortgage payments as well as hydro and phone with helps the stress levels. They are going to start slowly lifting restrictions to help the economy but if there are flare ups wit new numbers coming down with the virus they will ship it it down. Ontario and Quebec are having a tough go of it. B.C. Is doing better.
Lots of stresses in this new normal, hang in there and stay calm and stay safe.
Thank you Rita ,I am feeling better now the arthritis is in my joints, still got foggy head but okay Thanks, I already got psoriatic arthritis which not been a problem, but assume this is rhumatiod on my research with auto immune with mesh,I knew i was feeling rough but temperature was fine, wasnt until thursday it was running through my body, couldnt sleep and was having fever and gradually feeling my joints getting it,I wish i researched into this before they put the mesh in, i was told safe etc, they even knew i had auto immune diseases, still went ahead with it ,I may have to resort to disease modifiying drugs get better then ween off it as i got to work,I dont want use these at all but i dont want anymore pain or destruction in joints Yes i hope i am better soon too thank you
Tank you Linda, To think 4 days ago i was walking around etc like ususal , i just had to go to corona test and i am beat and pain in my joints thanks to NHS uk lol, I dont see any other choice but take strong stuff, Cant work cant pay bills ,I am sure plenty out there like this ,I just got get on with it, My wife is great understands and there always. 3 days feeling i want to end it , shes a gem , really is thank you :)
Hi Michelle. Sorry about the spots, i got those too from sanitisers,Yes i know lock down will get people bored and just eat a lot, I do now and i am still going to work but think its just boredom while i await my flakey wife to get to the uk :),Your winters are special compared to the UK, 25 degrees is summer here but can get a bit hotter in the summer for some weeks,Diane, Hand sanitiser can make your hands crack like mine have with too much alcahole, I need wash my hands at work all the time and put these products on ,bad too much but i do put moisturiser on the hands sometimes through the day just make them soft ori get old mans hands, Today is raining and cold which not usual as been hot for so long , Dont know how people will cope if lockdown on too long as they wont stay in , well you cant blame people as we dont get long summers though in the UK,we are still in spring but weather been nice. You take care too :)
When I was suffering, I used to run my house a lot cooler than normally expected. I use a urea-based skin cream daily and then took vitamin D tablets. However, this was also when I was on regular UVB treatment so I was a lot 'warmer' having been in the light cabinets. Now, I'm able to go short sleeves thanks to the biologics but obviously have to be much more careful due to the suppressed immune system...
True Elizabeth, we do have a invisible enemy. scary right? All we can do is to try and keep safe. wearing masks, using hand sanitizers, try to not touch our face....do they know how difficult that is for some? but here we are, we have to adapt and who knows what other virus is waiting for us. this will just teach us to stay healthy and try take others into consideration. This is not a thing of everyone for themselves but to think of others too.