I need help for an 83 year old man with severe PHN for 3 months
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Hello
I am writing on behalf of my father who contracted shingles in August 2015 in the right eye extending back throught the scalp on the right side. The neuralgia started as the scabs were falling off. He had intermittent excruciating pain at first but now is getting severe pain all the time - he is unable to concentrate on anything and even distracting himself with practical tasks, whcih helped at first is not helping now. He has been taking Gabapentin for about 6 weeks now - gradually increased the dose to 6x300ml tabs per day. I have done some reading on this site and have made a note of some of the drugs mentioned that have worked for people. It does seem like a case of trial and error. What I would like to know is how long do you stay on a drug before you realise it is not working - surely if Gabapentin was going to work - he should have noticed some relief by now. Dad is also on heart medication for severe heart failure - diagnosed earlier in the year - in fact the shingles came after he became very run down after taking multiple medications that made him very sick. He is also on Acyclovir and steroid eye drops for the affected eye. In the last week he has also taken colloidal silver?? anyone know anyhting about that for PHN?? - nothing he has taken so far seems to have given him relief - in fact it seems to be getting worse - resulting in him hardly sleeping at night. He is very fed up and is not enjoying life. He has been referred to a pain clinic but I have found out it will be a 3-6 month wait!!!
My other question then is can he be referred to a neurologist in the meantime - he lives in the UK. I live in Australia and have just returned home after being there for 2 months helping him get back on his feet.
I would like to thank everyone on this site for their wonderful support despite being in so much pain themselves - you are an amazing bunch of people
Alison
2 likes, 7 replies
jessica19028 alison11183
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alison11183 jessica19028
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wylee alison11183
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I would recommend signing up for the Ramsayhunt.org site (Ramsay Hunt Syndrome is Shingles of the Ear). We have a fantastic member from the UK, Jeff Hurst, and I suspect he could give you helpful info. The NHS can sometimes let things slide too much if you don't have a strong advocate.
Good luck.
alison11183 wylee
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And I will definitely check out the site you recommended - thanks heaps
alison
Jmac2 alison11183
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alison11183 Jmac2
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mmsmith alison11183
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