l had a phone call, from a friend with MS, this morning. She has been having monthly B 12 injections for some time. And they have been very beneficial to her - in fact she can tell when she needs the next injection - as she feels very fatigued. Her GP has said that she cannot have anymore as the NHS in conjunction with the MSSociety have stated that B12 injections do nothing to help her condition and are now being stopped.
My friend lives in West Yorkshire/Airedale. She has to go to Pontefract for her 'botox' injections for bladder control - and she has also been told that these might be stopped because of lack of funding.
She has requested that l ask you all on this site if this has happened to you. Because of problems with her sight she is unable to use a computer.
l have never been able to get B 12 injections as my GP says they are only allowed to give them to patients with pernicious anaemia. l do take a b12 supplement - but l do not think they are as good as the injections.
Hope someone can help