Postherpetic Neuralgia :: Cradle Cap - Shingles After Effects

Six weeks on after first ever attack of shingles at the age of 75, I am Completely physically, mentally and emotionally drained, despite plenty of sleep and rest. Appetite is fine. Still suffering some ache in head owing to an effect called Cradle Cap which I have been prescribed ointment.

View 1 Replies

Postherpetic Neuralgia After Shingles - Horrific Pain

I had shingles in October 2013 followed by what was assumed to be postherpetic neuralgia. I have tried all the various medication prescribed but appear to be allergic or react to all of them and none take you pain away. I don't know what to do next, seem to go from pillar to post. 

I had an xray done about a year ago as, (because I was involved in a car accident 3 months prior to the attack of shingles) it was thought the pain could be due to something else. It wasn't but the radiologist said that if I had a certain nerve 'snipped' in my back (left hand side) all should be well. Has anyone else heard of this. My doctor said they didn't have anything in writing from the radiologist to confirm this. I really feel as if nobody is much bothered about this sort of pain.

I do know for a fact that having nerve ends burnt off can stop pain. I had this done (privately when I was covered through work) in my neck which stopped the migraines I had suffered badly with for years. I no longer have private medical cover unfortunately. 

I can can only sympathise with others who have suffered following shingles. The pain is HORRIFIC but the advice seems to be to take pill after pill and then If that doesn't dork have another ruddy pill.

View 54 Replies

Postherpetic Neuralgia :: Shingles - Floaters And Blurred Vision

I am just recovering from shingles. I have never felt so ill in all my life or been so tired. I have been left with intermittent pain in my hairline where the blisters were and also in my eye. It seems to come on every afternoon and last all night. My eye waters and I have developed floaters and blurred vision. I have tried paracetamol which helps with the pain but not with the sensitivity to light and blurred vision.I go to bed with a cold damp flannel but it doesn't seem to help much, my scalp also itches unbearably.

View 1 Replies

Postherpetic Neuralgia :: Sweating And Upper Back Pain - Shingles?

My 88 year old mother who has dementia has developed odd sensations and pain in her upper back.  She's had two bouts of extreme pain which moved around but were in a similar area of her back - lower ribs on left side.  The pain lasted only for a day each time and each time I saw what looked like sweat pimples but they were on her upper chest at the front - ie a different place.  Now she often feels cold and shivery (when in fact she is hot) and puts more layers on to the point where she starts sweating, feels pain in her upper back and gets very anxious when she gets it (most days in the afternoon/evening).  She gets night sweats.   Does this sound as if it could be left over from shingles?

View 1 Replies

Postherpetic Neuralgia :: PHN And Low Energy

I've been suffering from PHN for about 2 and half years. The pain is mostly around my eye, temple and forehead, sometimes the top of my head. Lately I've been finding that I get very drowsy after an "attack" of pain. Does anyone else ever get that? I can't work out if it's an effect of the pain or a side-effect of the medication I'm on (which is a mix of Cymbalta and Pregabalin). 

View 1 Replies

Postherpetic Neuralgia And Edema

My 91 year old father contracted Shingles in November 2014 and from being totally independent  - living alone and driving a car he had to move into care as has suffered postherpetic neuralgia since. He has shooting pains going down the sciatic nerve in his right leg.  It seems like he has been on every drug known to man and although some of his pain has been alleviated he still has excruciating episodes.  His only means of relief is to stand so can spend hours sitting/standing/sitting/standing.  He has, however, since the shingles suffered edema in his right leg also.  Amazingly he still tries to maintain some independence and tries to walk, however, this is so difficult now that his leg is so heavy and swollen.  I don't seem to be getting any answers as to why he has this Edema.  He never had it before the shingles and although he had it mildly afterwards it is now extremely bad.  I'm wondering whether it could be the medications that he's on and would be interested if anyone else as experienced this and what the cause was.

View 4 Replies

Postherpetic Neuralgia :: What Makes It Better And Worse?

From reading many other threads, it seems to me that one frustrating thing about this condition is that there's no one-size-fits-all description or solution. Is there anything outside of heavy prescriptions that soothes your pain, and are there any triggers that make it worse?

Here are things that usually provide some relief:

1.Epsom salts compresses - help calm down the skin sensations

2. Rose geranium oil - helps with the skin pain and stabbing, and the scent is calming to me

3. Heating pad - helps when the pain is deeper, or maybe it just relaxes my tense muscles

4. Ibuprofen - helps with the aches

5. Acetaminophen - I don't think this works as well as ibuprofen, but I haven't given up on it.

6. Sleeping. I usually wake up at a level 0 or 1, and it builds up as I go about my day.

7. Sitting quietly. No friction when I'm not moving.

8. Exercise. Maybe it's true what they say about endorphins.

9. Sometimes stretching or scratching provides relief.

Things that make it worse

1. Coffee 

2. Lack of sleep

3. Possibly my hormone cycle; I'm not certain about this one

4. Sometimes, it's worse if I stretch, scratch, exercise, or sit still.  Yup, these are also on my list of things that sometimes help.   [eek]

5. Random triggers I may never be able to identify.

Do any of these things sound familiar to anyone else?   Or is there a good possibility this isn't PHN but something else?  Like, losing my mind?  

View 9 Replies

Postherpetic Neuralgia Survival Skills

Having deal with PHN now for 7 years it still is important to me to share information with others that are afflicted by this terrible condition or with others that suffer from chronic pain.  Important because it is reassuring is to hear how others are impacted and trying to cope in their lives.  It is terrible to constantly have to turn down or cancel social engagements because you cannot bare the pain, are so distracted that you can't focus on a conversation or do an activity that you enjoyed before.  You get tired of responding to people "how do you feel"  "how is it going" and many times you don't look that bad.  One doctor said PHN is like the pain of cancer but without the relief of death.  Not looking for sympathy from others but it is tough on family and friends given they don't really understand.  I tell people now best the pain of a stinging nettle and worst is like a bad burn/scalding and rubbing sandpaper on it.  People also don't understand (as I dont as well) why it strikes when it does.  Everyday for me - but usually later in day after I have had too much irritation from the clothes.  I want to say thank you to a number of people on this site for giving me my sanity back.

View 57 Replies

Skin :: Facial Hair Imbalance

My facial hair is imbalance. The sideburns on my left grows at a slower pace than that on the right.

Can someone please tell me what could've caused this?

View 10 Replies

Vestibular Neuritis - Inner Ear Due To Viral Infection - Imbalance

After 3 long months and what seems like an endless struggle to get diagnosed, I have been diagnosed with an imbalance between my inner ears due to a viral infection, leading to a diagnosis of vestibular neuritis. The doctor said my migraines could also possibly be presenting themselves atypically and aggravating the situation.

I am doing vestibular rehabilitation exercises and taking steps to unclog my sinuses.

This is the longest ailment I've had and quite frankly I'm fed up, I know rehabilition will take a while, however does anyone know how long this thing can last??? It's ruining my concentration at work and puts me off social situations (I can't drink, it makes me wake up the next day feeling extra dizzy)

View 2 Replies

Very Small Uterus - No Periods - Hormonal Imbalance

I am 23 years old and i have never had a period in my life. i have seen a gynecologist. first i did a scan and was told that i have a very small uterus they gave me birth control pills that did not work. they took blood sample and found out i have hormonal imbalance somewhere four times as much as they should be and others very low. they also asked me to monitor my temperature for 3 months and there were no anomalies there. my question is what exactly is wrong with me and does it have a name and will i be able to have children in future?

View 1 Replies

ENT :: After Stapedectomy, Back Pressure From Mouth To Ear - Imbalance

After surgery, whenever I belch with my mouth closed or sometime opened, a back pressure goes directly to ear that had surgery and cause a jolt of imbalance for about a second that scared me. Has this ever happen to any of you after stapedectomy?

View 2 Replies

Electrolyte Imbalance :: Salt Craving Else Feel Shaky

I just LOVE salt, and sometimes I feel a bit shaky and if I eat something salty, I'm fine!  I suspect this is an electrolyte imbalance, but no real idea. What's going on?

View 1 Replies

No Hormonal Imbalance But Weight Gain After Tubal Ligation

2 years ago I had a tubal ligation and since I have gained a lot of weight (especially the last year). Before the tubal ligation I was thin and no matter how much I ate, I couldn't gain a pound.

I have been to many doctors and I have checked my hormones (estrogen, progesterone, LH, FSH) as well as my thyroid MANY TIMES during the last 2 years.

My hormones and my thyroid are fine, and there is nothing wrong.

I have read about tubal ligation syndrome, but all these side effects after tubal happens BECAUSE OF A HORMONAL IMBALANCE  and I don't have any.,

Why am I gaining so much weight?

What about you that gained weight after tubal? Do you have hormonal imbalance or do the blood tests come back normal as mine do?

View 1 Replies

Vaginal Health :: Clitoral Discharge - Hormonal Imbalance?

I am 31 years old single...I have clitorial discharge and it was on and off is it normal?or my hormonal imbalance?

View 1 Replies

Electrolyte Imbalance :: Foot And Ankle Edema, Shoulder Muscle Discomfort

Does anyone have urinary frequency and/or urgency since taking pred? Like getting up every 2 hours during the night, and other times.  Also swelling of the ankles & feet?  Also stressful discomfort  over the upper back and shoulders?  Myi ankles have become quite edematous, I avoid all added salt.

View 1 Replies

Shingles From Someone With Shingles - Spread?

Hello! I am a 34 year old woman who has just been diagnosed with shingles. I have had them for about a week and am quite uncomfortable, but not miserable. I have had some stomach pains for a few days that I believe are associated.

One problem I have is in all the information on the net and from doctors they stress the point "you can NOT get shingles from someone with shingles"... well, I disagree. My mother is a non-hodgkin's lymphoma patient who was diagnosed with shingles about two weeks ago. I live by her and help her and I find it hard to believe my shingles didn't come from being exposed to her!

Just wanted to let others know.

View 5 Replies

Can't Get Shingles From Shingles? Spread?

I've just been diagnosed with Shingles. I have been told you can't get Shingles from Shingles, only chicken pox from shingles. But I am the third person in work in a week to come down with Shingles. If you can't get Shingles from shingles, how come so many people in work have it?

View 25 Replies

Glue Ear Tinnitus

Have glue ear anyone else got it? I am a 56 female in distress.

View 1 Replies