Hello,
Just wondering whether anyone would be able to share their experience of lymphoedema at the very start of having swelling please e.g. Was the swelling there all the time or did it come and go? At what point were you referred to a lymphoedema clinic? At what point was any treatment/management of lymphoedema started? Were you monitored for a period of time first with no action required? Did anyone have swelling that was being monitored for lymphoedema but it didn’t progress so no treatment or referral was required?
I discussed occasional swelling of my left leg, ankle and foot (mostly ankle and foot) and whether this could be lymphoedema with my consultant during my recent monitoring appointment and he’s made a note to check for progression at my next monitoring appointment in three months or I can phone my CNS if it gets worse before my next appointment.
This is my experience since surgery in February (radical hysterectomy for cervical cancer with 11 pelvic lymph nodes removed):
Most of the time, the swelling is very mild where it wouldn’t be obvious to someone not looking for it and is only more clearly noticeable when comparing with my right ankle and foot, which aren’t swollen. Other than the first few weeks after surgery when both of my legs, ankles and feet were really swollen but likely due to not being able to be very active at that point, the swelling on my left side has flared up on two occasions - towards the end of March and in early May.
In March, the swelling gradually reduced over the course of a week to 10 days through elevating my leg and regular walking (as advised by my CNS) - the swelling completely went down so that my left and right side returned to looking exactly the same as each other. The week before this swelling, I’d had a bad week in terms of post surgery pain and fatigue so I hadn’t been very active so I put the swelling down to inactivity.
I was really disappointed when the swelling returned at the start of May as I was much more active by this point (back to dog walking, averaging 6km per day). Again, I elevated my leg and kept active. This time, the swelling has been much slower to gradually reduce - it remained at a mild swelling level for a month until yesterday when the left side finally started to look close to the same as the right side again.
I guess time will tell whether I’ve just experienced some unconnected occasional swelling, whether the swelling is due to lymphoedema and whether it will get any worse than this mild swelling which eventually reduces.
I’ve done some reading about lymphoedema on reputable websites so I have general information about it, but it would be good to also hear about other people’s experience of early/mild lymphoedema if possible please.
Thanks and best wishes,
Louise
Hi Louise/L2025
I’m Anne, one of the Community Champions here on the Online Community and, although I'm not a member of this group, I noticed that your post hadn't had any replies yet. Responding to you will 'bump' it back to the top of the discussion list again.
Hi, I've been diagnosed with lymphadema in my stomach. I had lymph nodes taken from my groin. So far it hasn't found a channel to drain. It's very uncomfortable. I had a referral from my cancer nurse, I did have to push for it. At this moment I don't know if its long term or permanent.
Hi Lizzy58
Thanks for your replying. Sorry to hear about your experience with lymphoedema. Thanks for letting me know that you had to push for your referral - sounds like I might need to do that too. The swelling that I mentioned in my post that had just gone down after a month only stayed down for two days and is back to being swollen again now.
Louise
Hi Clem16,
Apologies for being slow to reply. Sorry to hear that you’re experiencing swelling in one leg too.
Not much has changed for me since my original post. The swelling goes up and down (but never completely normal, my left side is always at least slightly bigger than my right side) and my left leg feels heavy and an effort to move (especially going upstairs) when swollen. My left calf feels quite hard/tight and different to my right calf. Indentations (e.g. after removing socks or boots) are more noticeable and stay for longer on my left side than on the right.
I haven’t been referred to a lymphoedema clinic as I’ve been told both by my GP and hospital consultant that the lymphoedema clinic wouldn’t do anything at this point other than check regularly for it getting worse. I have it in my notes for this to be checked each time I go for my three-monthly checkups at the hospital. I’ve been advised that I can buy compression socks to help the swelling, to elevate when swollen and to keep being active without spending too much time standing.
So, although a bit annoying, it’s fairly manageable for me at the moment. The only problem it causes me is with driving as I drive a manual car and my left leg/ankle does not like having to operate the clutch at all so this limits the amount of driving I can do and therefore the amount I can work at the moment. If I could afford to, I would change my car for an automatic or electric car so that there’s no clutch, but that isn’t possible at the moment so I’m just doing my best with driving only short distances (where I live there isn’t much public transport as it’s a fairly rural area so I need to drive to get pretty much anywhere).
Has your swelling remained the same since it started or got worse over time? Has your GP/consultant given you any advice yet? Hope your swelling either goes away or is manageable.
Louise
Thank you so much for your reply. I'm so sorry though that you are in a watch and wait situation especially as it's impacting on your daily life. I can well imagine that being on the left side driving is an issue. I'm on patient initiated follow up so it's up to me to get in touch with the hospital if I need to. Mine has improved a bit as my foot pain has receded but the lower leg is still not the same as the other one. I'm going to keep an eye on it and maybe contact them at some point.
To be honest I was thinking this group would be busier than it is as the statistics for lymphoedema for some of us are quite high!
Did they tell you anything about how to get compression socks as I thought they needed to be measured carefully?
Thank you again for getting back to me. It's made me feel not so isolated.
Glad to hear that your swelling has improved a bit over time. Hope it doesn’t get any worse for you.
I’ve also been surprised at how quiet this group is. I guess many people either aren’t in the online community any more if they’ve finished their active treatment or stay within the group for their specific cancer type. I’ve had messages from some of the ladies in the cervical cancer group who have developed lymphoedema post surgery.
The proper compression socks that are used for lymphoedema are the ones that are measured and fitted by the lymphoedema clinic. It was suggested to me that I could try some general off-the-shelf compression socks (e.g. flight socks) to see if they help. I haven’t bought any yet but I’m going to give them a go to see if they help at all.
Louise
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