Hi guys
For those following you already know the recent challenges faced.
On Wednesday 21st November 2018, I put in request for repeat pain relief medications. According to the practice rules this gives them more than ample time for doctors to respond to Chemist request and all medications not included in blister pack to be dispensed.
First challenge:-
1. Telephoned Chemist who during our conversation rudely stated: He didn’t care whether or not the doctors did prescription! 😱 Believe me not taking things out of context or being melodramatic. As a matter of fact, am putting his attitude/behaviour rather mildly!
Step 2 - telephoned the surgery and spoke to their receptionist there who told me that he had no business speaking to me like that. Whilst she is sorry abt my experience, she would not take my request but rather told me to call back the Chemist as he needed to put the request in writing on my behalf 😧
Step 3 - Medications are delivered on Fridays. When the courier came there was no pain medications whatsoever - just blister pack. By the time you can fully appreciate the extensive excruciating pain am in. My sympathetic nerves has now started to give me sharp sticking pains under my left rib cage, my body and hands cold and hands started turning blue.
Step 4 - explained to the courier my plight. Even showed him the empty bottle and gave him the empty boxes and message to relay to the Chemist that the meds were needed urgently. In the Chemist defence, the courier said maybe you will receive it tomorrow - that’s today.
My carers are now beginning to feel my pain again trying their best to make me as comfortably as they could knowing the pains will keep me awake for the 3rd night running. And expressed their frustration saying this is abuse and they didn’t like what was happening to me and would need to report it to their agency.
Step 5 - Weekend carer came on duty. Her first question was did you receive pain meds? Said No. she was furious. By this time any movement made however small was excruciating.
Telephoned the Chemist. He stated: wait for it: No doctor in that practice wrote up the prescription. None. He said he went there twice but none was given for me! 😳 He went as far as to check his computer system again, still there was none on the system. Said very little he could do and rang off. 😭😭😭😭
My last resort was to press the security alarm button who in turn dialled 111 and the whole procedure of processing carried out for me to receive what’s a routine prescription in order for me to have and be on top of my pain management programme. 😐
Please has anybody had to ever go through this whole shenanigans just to have & maintain your pain management programme?
The Raynauds, Lupus, Hugh’s Syndrome, sympathetic nerve, flare ups are at their highest
Asked 111 clinician for a Lupus specialist who understands Lupus to be contacted. She said there was an on- call doctor who would contact me from SW area. If anything further developed, I should return the call to them. What are they waiting for? For me to keel over and die? This is over 1 1/2 hours ago. Still no call. No meds. What other course of action must I take?
What other means can Lupus UK do besides round table talks with GPs?
I’m truly suffering here and am not the only one. 😭😭