Hi i.m having my pip tribunal soon waiting for date had all forms this morning the thing is the doctors report is dated the day i was told i finally had uat the 27th of december so shes only put what i was suffering from upto that point . Two weeks to the day i started having pins and needles constantly then loads of other symptoms just got worse i even asked on here about it and was told b12 etc. So back to doctors had my vits tested and found low in vit d iron calcium ferratin folic my b12 was 231 doctor wouldn.t treat me so self treated and i much improved. She did put mind that i had uat and no long term disabilitys will be affected with this it was as if she as it but its not going to affect her at all i.m so fed up of not being taken serious with uat people always respond as if its nothing . I told my doctor about me walking upstairs i said my legs kill me and i struggle to get upto the top and i.m out of breath also but if i.m walking on the flat i can walk for ages my legs will kill later on mind but it don.t affect me like hills or stairs . What i want is some links i can print off and send to my appeal so they know about b12 affects on the body and vit d and uat / hashi.s the best ones really like telling you the long term affects on the body the symptoms you can experaince and why going gluten free helps the body with out pip i can.t afford to go gluten free its just to expencive and my coeliac test said i was fine. I.m having to buy my own vitamins cause the doctors ones are rubbish low doses and not the ones you should take and they ate not cheap to buy and am to embarressed to say how down i am to the doctor he don.t take my uat serious and i put on a brave face to him and everyone saying i.m fine cause i have family yo look after but i ain.t i go to bed some nights and cry myself to sleep i hate how i always feel tired and worthless and having to rely on the kids to remember things all the time i just hate it i feel so old on times x
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