Breaking a taboo

It’s taken me quite some time to dare to write this post; it feels like such an unmentionable topic. But, I’m coming out… I have genital warts. There, I’ve said it! Phew! But, don’t fear, I will NOT be posting any photos this time! 😉

I’ve felt very reluctant to go public about this particular issue, for reasons which you will understand. Many readers may even think that this is just way too private and perhaps I should keep it to myself. But it’s part of my myeloma journey, and I want to be open about the whole experience. I’m also aware that other myeloma patients read this blog and it feels important to share so others can benefit, if only to know that they’re not alone and it’s ok to speak about.

It’s quite simple… my immune system has been suppressed due to the disease itself and even more so following two stem cell transplants. It is now and will continue to be compromised, so I am particularly prone to fungal, bacterial and viral infections. I now fall into the group of people who are entitled to an annual flu jab (which I’ve already had this year). I also have to take prophylactic antibiotics (Penicillin and Pentamidine) and antivirals (Aciclovir). While the antiviral medication will gradually decrease over time, I will be taking antibiotics for the rest of my life. These support mechanisms don’t eliminate my chances of catching an infection; they simply support my immune system and thereby lower the risk.

I became aware of the warts in April and mentioned them to my consultant. She was very keen that I have them treated and ‘get on top of them’ prior to the transplant, as they could readily proliferate and be harder to treat following the transplant, due to the lowered immunity. She referred me to the genitourinary medicine (GUM) clinic, otherwise known as the sexual health clinic. The doctor I saw is married to one of the haematology doctors, so she understands well the process I have gone through and the connection between my disease/treatment and my sexual health.

Initially, the doctor suggested using Warticon, which is a cream I could apply myself. They even provide a wee hand mirror so you can see what you’re doing. I didn’t see much of a response to the cream, so the doctor prescribed Aldara cream, which is used to stimulate the immune cells to manage the virus that causes the warts. That didn’t work either.

I had a gap in treatment while I went through the transplant and in the first few months of recovery from it. But since the end of September, I have been going for weekly treatments of freezing (cryosurgery) by a nurse. They spray liquid nitrogen directly onto the offending areas, using a ‘gun’. It don’t half sting!!! At last, it does seem to be working; they are vanishing. In fact, it’s working so well, that they gave me a week off! 🙂

Because freezing kills off all cells it touches, the healthy skin around the warts is also affected, and the nurse was concerned in case the skin broke or became painful, so she gave me some aqueous cream to use as a wash. It’s very greasy. In fact, when she advised me to ensure I washed it off after use, she explained that if I didn’t, I’d feel ready to swim the Channel… like being covered in goose fat!

I’ve asked questions and done a bit of online research too. Here are some of the answers that I wanted:

Many adults are likely to have encountered a range of viruses, but only a small percentage actually develop symptoms. This is the case with Human Papillomavirus (HPV) that causes genital warts. Most people are exposed to the virus during their life, but it has the ability to remain latent within the body over long periods – even years or decades before developing into warts, so it is usually not possible to determine exactly when, or from whom, an individual contracted the virus.

For most individuals the immune response appears to dominate and lesions (warts) never develop, or they develop but are suppressed by an immune response before the person ever realises their presence.

Other viruses that can lay dormant without causing any ill effects are Herpes Simplex (HSV) and Cytomegalovirus (CMV). I mentioned in my post “A walk in the park…” that both my donor and I were screened for CMV prior to transplant, as this can be life-threatening for the immunocompromised, whereas it typically goes unnoticed in healthy people.

I also read that persistent infections of HPV may lead to cervical cancer as a result of cellular transformation. The last thing I need is another cancer, FFS! So, it’s critical that to knock this thing on the head. I’m off for another bout of freezing on Thursday. Ouch!

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About Jet Black

I began blogging because having been diagnosed with Multiple Myeloma, I wanted to share my experiences of living with an incurable cancer. Through blogging, I discovered that I enjoy writing. I have always chosen to live life for the journey, more than the destination. This is as true for the act of writing as it is for living with myeloma, so these are two things I do: I live and I write!
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7 Responses to Breaking a taboo

  1. Jet – it is so good to read such down to earth descriptions of your daily living! EspeciLly written with humour and straight forward facts. I am lucky not to have to go through this process but let’s face it – there but for the grace of god go I? If we haven’t been touched by cancer, we know someone who has – thank you Jet. Helen

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  2. Mary Pat Druschel says:

    Jet, Wow, I commend you for sharing this very personal but very real challenge. My sister had a similar problem, I hadn’t thought of it in quite a while, getting anyone to address it was not easy. I think it is much more common than people might want to admit. It’s an important issue to bring up, so good on you. You are truly one in a million Jet, thanks caring about everyone else enough to tell this pretty personal part of your story…

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  3. Brave, Jet! And there is so much more about compromised immune systems that people don’t know… thank you for sharing the info and NOT the pictures…LOL!

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  4. Morag says:

    Eek! Cryosurgery sounds painful. Hope it gets better soon so you don’t have to have any more!

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  5. Cathy Naumann says:

    Excellent coversage of a sensitive issue..and I give you credit for being honest.I hope it heals for you soon..And again thanks for no pics!!!

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  6. Nancy Lange says:

    Jet, I didnt find it offensive at all. It is your experience being shared for the benefit of all. As a nurse, I felt it was well written and informative. Can empathize with the histo freeze….I have done this to oh so many of my patients in the past. Ouch Best wishes, and keep pluggin along 🙂

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  7. Sandra abraham says:

    Thanks Jet for your blog on this subject, I’v got a few warts on my hand and tried different things to get rid of them. The last thing is the freezing treatment as I’v heard its very painfull so what it must be like down there must be hellish !!! Keep blogging Hun xxx Sandra.

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