Sharing my experience - recurring shingles

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I'm a 35 year old female and have had recurring shingles for about 7 years which occurs anything from 3-7 times a year and occasionally back to back. It is always a small cluster of itchy/stinging spots at the base of my spine and thankfully, the only other symptom can be overly sensitive skin down the back of my thighs. It is the only 'illness' that I ever suffer from - I never get colds or other 'bugs' that seem to plague everyone around me. So, the main guidelines about shingles are very general and should not discount anyone who suffers from this if they fall outside the norm for the condition i.e. over 50, poor immune system, you only get it once, spots appear on the sides, chest or face etc. as I don't fit any of these but have had tests and confirmation.

My advice to anyone else who suffers from this is - do try to get antiviral medication like aciclovir as it will minimise the frequency of outbreaks, try the coldsore patches from the chemist (Compeed is the brand I use) - they can be costly but keep the area clean and covered to prevent spreading and definitely seem to clear it up more quickly and with less scarring and, finally, try not to touch the area at all outside of treating it. I have become good at recognising the early sysmptoms and the earlier I act on it, the less troublesome it is. I have also made a connection with using sunbeds as a couple of outbreaks have occurred shortly after using one so minimise UV exposure of the area (not usually a problem when it's on your bottom!). Hope this helps.

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  • Posted

    Having read up on shingles it would appear that it is stress related and when your immune system is at a low level so to this end I taken up what I have been told, that MANUKA honey is good for your immune system and this would seem to be the case according to my local Holland & Barratt shop. So I am giving it a try, certainly the pain seems to be a little less and my arm is at last showing signs of improvement so its worth a try. I have a tea spoon of honey in hot water at bed time each night, I have just started my 3rd week

    Be wary of where you purchase it from as prices can vary considerably, best price I have found is Aldi for the +10 strength

  • Posted

    Im 35 and I just got shingles for the 21st time since 2013. Its always around my eye. Im so tired of it that it makes me cry. Im sick of the pain, sick of feeling sick and sick of having nasty blisters around my eye justabout every month.
  • Posted

    I have battle shingles for more than 27 years. This year did get the vaccine and have had several outbreaks, but they seem to have subsided for now. I know that my insurance Blue Cross has changed their policy about the shingles vaccine and now covers it 100% regardless of age
  • Posted

    I need to check into that. I dont have insurance yet and the county health program sucks.
  • Posted

    18 years of several outbreaks of shingles a year, three since December 2013, has been quite a trail. I can relate to every single post here.

    For the last three months I was treated with osteopathy against the pain and it certainly has helped.

    I found the posts with dietary tips very interesting, especially the ones on lysin. I´m going to try that.

  • Posted

    Good luck. I hope it works for you!
  • Posted

    I had my first bout of shingles at age 15. I will be 55 next month and have had 3-6 outbreaks a year ever since. So WELL over 100 outbreaks. Almost always on my right upper eye lid, although it has occurred once on my spine and a few times on my forehead. I'm on day two of the latest outbreak--so wish I could put a stop to this 40 year saga.
  • Posted

    I have had shingles too many times to count, the more I get them the worse they get and the last 3 times they have become infected. I haven't found any remedies though vitamin b12 injections daily do help clear them up, my doctor won't give them but someone may have some luck. I have had immunoglobulin tests to see if there is any deficiency, they are all within normal parameters it may be an idea for some of you if you haven't had any tests. My doctor is really good but confused at the same time I am his only patient that has recurrent shingles so I think he would like to find a reason. There is some sort of link between rheumatoid arthiritis and shingles as they are both autoimmune, this increases if you are being treated for RA as the drugs depress your immune system further. My doctor is definitely on the case so I will keep posting if he finds anything that helps us, he is meeting with haematologists this week.
    • Posted

      Check out "leaky gut" I believe this may be my problem, but I have not been able to try and fix yet.  I don't know your lifestyle but it may be worth a look. 
  • Posted

    I just turned 37 and have been experiencing recurring shingles for just under 2 years. My first experience was 2 days before my wedding. I felt a sharp pain and noticed a few clustered bumps, within hours more tiny blisters popped up. Since then, I've had 6 more times. I've been to three different doctors and they have done skin samples (ouch) and blood tests. I've come up positive for herpes 1 (the cold sore virus) but my blood tests came back negative for zoster - but looks and acts just like zoster and I've never had cold sores of any kind. None of the doctors can explain or really know what to do. I have been given acicyclovir but I don't really think it helps. Each time I feel like I'm coming down with a cold or feel rundown, it ends up an outbreak. Each time this occurs on the lower left back in the size of a quarter and luckily hasn't spread, just might be a little to the left/right. Currently I have a new cluster right next to one that has recently cleared up from the beginning of the month. I had a very severe case of chickenpox as a child, so doctors think that that contributes. I've tried to think of anything/everything and am baffled as I exercise regularly, am rarely sick, eat healthy, etc. My job is stressful, but my life is pretty "normal" otherwise. I try to think of anything that could be a factor (I did tan before my wedding in a tanning bed) and have gone a couple times since, but don't think that is the cause? I get sharp pains followed by tingling skin and at times it's hot to touch. I think I've become accustomed to the pain but it's very depressing and I've gotten to the point where I don't talk about it with friends or family anymore because they just tell me I need to reduce stress, take vitamins- everything I already know. I just take the pain and keep my mouth shut. I'm sorry to see I'm not the only one dealing with this, but am glad that others have shared their experiences because many are quite close to mine. I continue to take pics of the progress to track and hope to find a doctor that can help me. Otherwise I'm very healthy, but am getting down on myself and have stopped sharing my concern with most, even my husband. I also have experienced sore pain, then sharp shooting pains with mild itch. I haven't tried any creams (one doctor said it won't help) and I've kind of given up. Took a couple acicyclovirs last night but never really notice a difference either way. I hope that you all find a remedy that works for you and can sympathize with your pain, confusion, etc. I'll keep pushing through and hope they will stop one day. Thanks for reading my story.
    • Posted

      My dear,the same is happening to me as well...size of a quarter,stabbing/burning sensation before it occurs,feeling very tired2,3 days prior to it. All started when I was 18 years old,on my right leg.Now I'm 25 so I've been dealing with this  for 7 years now and I've tried everything possible. I'm living a very leahty life style,no animal products at all,no drugs,no alcohol and I simply can't find a logical explanation for this terrible thing. For many years  my doctors and I thought it was Shingles but then I started getting it more and more often (every 3 months) so now they think it may be Herpes Gladiatorum,but we are not sure,waiting to get it again so they can test for it and see. As a baby I had a very mild episode of chicken pox,fallowed by a severe case of Zoster herpes(Shingles) I was about 1 year old when this happened and it was on my left leg,back then people didn't even know what it was,being born in Romania my mom had to take me  to a private hospital to find out what it was. Today I have terrible scars on my inner tight,left leg and permanent numbness all way down to my knee. I don't know if these two are in any way related to each other but it feels like a curse anytime I get it and I just wish there was something to help us all. God bless everyone.
    • Posted

      I am sorry to hear that you are having a similar experience. It's exhausting. I am breaking about every 5 weeks - same spot, around the same size and same symptoms as you describe (flu like symptoms, rundown, etc). I wonder if your childhood chicken pox/shingles have stayed dormant for all these years? I wonder the same about myself. I went to my 4th doctor last week. She retrieved my past health records and noticed that my skin culture showed positive for HSV-2, although I've never had genital herpes, and HSV-1....no zoster. However my lab results from my bloodwork are only showing HSV-1. They are also looking into herpes gladiatorum which after researching, sounds very likely. During my first outbreak (right before my wedding) I was working out at the gym a lot, as well as taking a mat pilates class. I will be the first to admit that I am not one of those people that is overly cautious of germs, etc. but did have some reservations of using the gym mats. 

      I just picked up a prescription for suppresive treatment and am hoping for the best. I guess I still don't really know what I have going on at this time since my blood tests and cultures are conflicting. I would think that since it's been almost 2 years that my body would have built antibodies for this by now.

      Keep me posted and good luck to you!! 

    • Posted

      As a child I didn't experience any repeated episodes of Zoster Herpes or Chicken Pox,it all started after I turned 18 years old and since then every 3 months I get an other miserable breakout on my leg.I didn't use to be cautious of germs or anything like that,but after 7 years of dealing with this and always wondering what could be the underlying cause of it,I became paranoid and to be honest it's affecting my personal life big time.I m so sorry to hear that you are getting breakouts so often,I understand exactly what are u getting trough and I wish we could all find a cure for this once and for all. Wish you all the luck in the world my dear and please keep me updated,I will let you know once I find anything new. Best regards
    • Posted

      How is the suppressive medication working for you?   I've been trying valtrex and I may need to switch to Zovirax because the valtrex doesn't seem to be working

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