DONT MAKE ME ANGRY, YOU WONT LIKE ME WHEN I AM ANGY, I TURN VERY FLAKEY I am a maintenance operative in my job, i am a plumber by trade.I have had psoriasis all my life since birth 50 yrs, psoriatic arthritis 16 years.
I didnt know as this is what all them do, shove mesh in , I declared i had auto immunedisease and i should had been turned away, neglegigence this is , I am making a complaint to NHS uk against the surgeon too, There are many who have mesh and have auto immune diseases believe me because this is standard practice now for 30 years , Someone told me here they have too had mesh too , its russian roulette and its a matter of time before it happens then your screwed,live with auto immune response which is really bad with mesh or get it taken out with more risks even death though it wont matter if you are asleep anyway as you wont notice until you hover over the surgeon killing you . Glad you slept well Rosey :) glad you are better Rosey :) Thanks
psoriasis is all trial and error with docs Rosey , If you are not getting anywhere then dont bother with them i say , I dont see them for psoriasis as you know, not done for years but now got to deal with them because of what they done to me ,Bad psoriasis is hard i know and i am lucky that i havnt had it bad for 30 odd years , Hope you will be okay ?
Thanks Rosey , Yes i do cod liver oil too for got that one, I been eating fish everyday too also and less chicken,Luckily my skin isnt a big problem, in the winter it can get bigger and sore , considering i have had no sun on my body accept my arms it been okay,Funny Doc said whats that rash? idiots dont know i got psoriasis hence psoriatic arthritis? dont they look at my history?, he was saying i got stuff to clear that? i said no thank you i dont want chemicals,oh? well if i was desperate a got some chinese steriods lol,Sounds like you are doing a lot for yourself Rosey :), keep at it as it maybe helping a little, try probiotics, think they help me you know .Yes save your money on specialists, waste of money all they will do is give steriods, suggest sun beds and stuff,Yes if you got fatigue ashwanda i told does help so me i try anything within a degree, Different meaning everyone s unique no matter what they have to deal with , its the person not the disease that makes someone and bad psoriasis and say arthritis has huge impacts on life and people out there will not understand, My boss never understands, hes an idiot, thinks that exercise, stretches will sort out bad inflammatory response with joints, hell it wont,I am going through a lot Rosey but i have made my situation better thank you , i am awaiting reumatologist to see me as i know i need feel normal, my eyes have pressure not bad and blurr vision when trying to read even though i need glasses, i depend on them more, sun is a nightmare for my eyes so now where sun glasses a lot now at work,i think my eyes feel better a bit, i get tired all the time, dont sleep well,get groins discomfort from mesh though not painful at the moment,its taken a lot of my life away and i could suffer as a result when eventually i get ths stuff mesh removed, if they can remove it all?, its not a simple operation and takes a specialist ,i need it gone for my immune to recover for better , if they cant remove it all then i am stuck let alone complications i could get when i get this mesh taken out eventually,they shouldnt had put it in me but i found out months ago that this is a common problem with people with auto immune and mesh implants , I am going to complain to Nhs uk as i have proof that i declared i had auto immune and surgeon should had said no cant do it you need this operation , i been damaged since day one then recent auto immune,if things go bad then i will not stay on the planet as quality of life is important to me and not live sick, I said to doc i was healthy in good condition before this surgery and now i am ruined, hay ho,Yes thank you , yes i hope Michelle is here too soon, still waiting and i have her support too cant wait Rosey for her to come to her home ,We do the best we can under circamstances and thats all we can do, unfortunately the NHS has destroyed me in many ways but i see how things go , Thank you
Its okay , Just hope your Doc is good because all mine i see are useless, I never needed them for years and now i needed them and i got lied to, serious yes lied to, i found this one Doc out, One doc the one who sent me for the hurnia medieval torture 2 and a half years ago did give me an examination and confirmed like i dont already know that i have inflammation which he found in my lymph nodes, Docs can make you look like you are crazy, I said i was healthy before this operation , no inflammation of arthritis, no uveitis, no fatigue, no weakness and joint discomfort and now all that crap but i have taken some control on it,Doctors Doh , dumb asses in my opinion , So as i always said for years that docs no nothing, i have to tell them stuff as they dont know, and comfirmed i has swollen lymph nodes like i dont know i got inflammation lol, Just hope your Doc isgood because i will change mine in the future assuming i am still alive lol, Glad you got no itch, Yes i have heard these do help, Strange thing is my skin is getting so much better but, i am taking ashwanda pills, probiotics, B12, more magnesum pills, turmeric pills and adding turmeric to my food with garlic and ginger and onions thrown in, could be helping my situation mainly skin, worth a shot you know Rosey ,I take biberry pills also for my eyes daily ,Yes i knw what you mean when you want relief Rosey, i am waiting for that too for my immune response
My answer to so called specialists Rosey is they are or most of them a joke and your pharmasist should show compassion and not shock by what she sees,Not professional making you feel uncomfortable and upset , Bitch i say she is sorry to say that , I had that reaction from someone and i stayed calm but i was hurt inside but had to think, what something bad happens to them ?if its to the face skin what ever , their life would change but they would understand what its like for those misfortunate People and got understand no one can help going through this shit and you want help, I am disgusted by this. mothers. I hope the antihistamines help you Rosey and just think those that show no compassion but look as though you got something contagious are shallow especially those in pharmacies that should give sound advice and show professionalism to you as that what they get paid for and not make people feel uncomfortable as that hurts, i am with you on that been there worn the flakes,
Thank yu Rita, I still feelrubbish but better rubbish lol, mainly because of eye strain vision problems from all this toxic mesh but ,i am better Thank you ,It has taken some of my life away and some i will never regain it back as a part of it is near lost and will more than likely be fully lost after removal, I have to think positive though i know,I have had many tears over this for a while and wish i knew how dangerous this operation is was for woman and for men too, I should had never trusted the NHS to do this but i knew no different like everyone, Most meshes are used for repair but can lead to concequences especially with an auto immune and a lot of mesh victims end up with auto immune problems that werent there before and can be life threatening , dangerous, I will have to wait a long time to get this removed from me, maybe a year i dont know with back logs and covid stuff its worrying? , I just wish i knew, ,90 % of hurnias are repaired with mesh so theres a lot of people suffering like myself, Thank you Rita
Just thought to let you know that , I have cured my irritable bowels, thats was rough. I havnt had an inflammatory attack in over 2 weeks now, I am trying different things to help my self, bilberry pills, Flax seed oil and of course my lifestyle which helps anyway , I do feel discomfort of course but managing sleep better, uveitis is annoying and makes me tired, brain fog is slight, joints feeling a bit better, I am waiting rheumotologist as i think i still need a biologic?i stopped anti inflammatories, anti depressant, anxiety drugs a while ago though i will take naproxen anti inflammatory if i need to but seems i can cope more now, groin disconfort is still there from mesh but not huge pain so i can last the day with rest at times at work, my employer said rest as much as you can.I could be waiting some timesget mesh out as there is a back log of people, I am scared as it could cause me a lot of pain and possible damage get this out, it all needs to come out or its pointless as my immune will never be calm none existant as it was before mesh though my immune abrupted recently within 2 months, i do have control touch wood , knocking my head with my hand not too hard lol, Its very scary but i am in catch 22 , leave mesh possible more problems with immune and what ever else? take it out more pain and problems, possible death? I am not the same since day one of surgery and has time has passed more problems thats arisen but hay ho
True my lief your right, Does help to rant it out here on flaym :) , part what its for then take advice if one wants it? ,I just wish my healthy eating would help now lol but with your advice on drinking turmeric and i did get black pepper but corns, nice and chewy whole lol and some cumin put in there in my foods yummy , it did help, i been dosing on pills too try build my self up and zap thoughs invaders in me, bloody buggers, I teach them when i get my Immune suppressing drugs, Take that and this you nasty cells my gorgeous lief xxx :)
I just hope i dont have to wait long for help, as i am an emergency case or i be out of work. i hope to be in this week but who knows?, Now we are level 3 also i beieve , Just hope i can get in quick,Dosnt help people mingling on beaches now all close up together spreading the virus, look in the british papers unbelievable
Thanks Rosey, Yes i have no choice but get it out, Yes we psoriasis people tend to refect anything thats put in the body, i wish i knew before i had it done, its not simple, they could damage my intestines, blood vessels and nerves which is more likely possible or kill me lol, Like i have said to people its not like taking out a kidney stone,They could do more damage to me but i know i got to take chances or suffer arthritis bad all my life, Well i did a lot of research on mesh and implants etc,If you already have auto immune problems these can manefest themselves worse as seeing the object as an invader which is what has happened,Well you think my arthritis was great for over 3 years , none existant,all with eating well no inflammation, skin is different though though not bad as some,I cant help my
self with my lifestyle though with this in me,would it be worse than it is now ifi didnt eatwell?that i dont know? My feet are playing up too, wrist and thumbs aswell as everywhere else especially my back and neck, Why i got get meds in or i cant work and i have too, luckily my job is not hard and i can wonder off sometimes at the moment ,.
Thank you Rosey for saying nice things , i hope you get well too, This is the only place i talk about this aswell as warning others of mesh on youtube :), I have saved a few people from mesh lol. Thank you ,Well we all need help dont we even to listen or say read lol Thank you :)
Hello Rita , Yes ihave to do blood test thursday to check for inflammation, then once they find that then rheumatologists at some point and probably be put on bilologics as i need to work ne normalalish lol, I really wish i didnt have to go through all this ah well,Well i dont know how things will turn out with mesh removed as i dont here anything good about it accept one case thats it ,I get one thing sorted ie arthritis but could end up with lots of problems from mesh removal,I know igot get it taken out or i go blind too aswell as all other problems with arthritis ,If things go badly then i decided i am not going to stay here , it could effect a lot of things Rita, All this because of mesh,I am trying to be positive though but dont expect too much,i dont give up easily. Michelle maybe herein 2 months time ? Still awaiting visa Thank you Rita :)
Thanks Rita, I live :).Well i got blood test next thursday to check the inflammation level markers, Then i be sent to rhuematology and i expect i be put on biologics as i cant cope well with fatigue that this is giving me is the worst , resting i am fine but work noooo, I never agree with biologics but i think theres no choice as i cant work like this , not easily anyway , Skin . arthritis i can deal as i am tough cookie :), fatigue no its worth that the arthritis but i have some time put up with and i got deal with work etc, Luckily my wife is great , shame she is not with me but in time she will be Thank you :)
If i get Covid 19, I think i am done for,I dont think my immune will take it, My risks of getting it is high as i work in a nursing home with staff bringing it in and giving it to residents, I have to go in some of these rooms with it, Not good , So if i do get it, I think i will meet our maker, Trying my best though not to get it :)