Lipoma :: In My Back Grew From Pea Sized To Golf Ball
May 16, 2007
I recently had a Lipoma in the middle of my back to the left of my spine, which was pea sized but noticeable to the touch. Over a period of about 5 years it grew to become about the size of a golf ball or slightly larger (things always feel larger inside don’t they!)
I was annoyed because a doctor at my surgery explained that it couldn’t be removed by the NHS, only private as it was classed as a 'cosmetic' operation. I sought a second opinion from my own doctor who said no, it should be removed and could be removed on the NHS; as it was causing such discomfort. I couldn’t believe the first doctor could even think that something ‘about the size of a tennis ball’ (as she put it), which was obviously causing discomfort and could be seen through clothing, could be was classed as cosmetic! (If this happens to you, demand to go on the NHS or see another doctor!)
It was uncomfortable, not really painful, but it certainly felt like someone had left a tennis ball inside my back! I could feel it as I leaned back in a chair and with deep breaths, it felt like it was pushing against my insides (not very pleasant). By now it has also started to be visible when wearing a T-Shirt (as a bump), so I decided it was time to get it taken out.
Within 2 weeks of visiting my doctor I was in surgery. The operation was no problem, even though the anesthetic did hurt!!! (but I’m a man so I’ll soldier on!) After the op I was in Tesco’s shopping … but about 8 hours later, when the anesthetic had worn off, it bloody hurt! It was hard sleeping – I had to sleep on my front for weeks!
It still feels like something remains – its like a 6th sense and I can still feel something in there, but that may either be my imagination or, as I was told, part of the Lipoma that couldn’t be removed.
At the end of the day though, there’s no need to worry about the op (and I’m the biggest coward going when it comes to hospitals!) – it was simple and not too painful … and the hospital staff were very friendly.
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Over the past year, I've developed migraine- like headaches that completely incapacitate me. For the most part, these would come on a frequent basis but I could go about my daily routine without disruption...until about four months ago. The headaches became non-stop. There is no break in the pain (the doctors don't understand this concept- they keep calling them "episodes"). The intensity changes, but the pain is ALWAYS there. I've been treated for migraines, but the medication for it doesn't work, and the pain isn't quite the same as a migraine. It's very hard to describe...almost like a twisting sensation in my skull and across my forehead.
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