Pain in heels.. Interferon related or not? - MPN Voice

MPN Voice

10,886 members15,202 posts

Pain in heels.. Interferon related or not?

beckyluck profile image
17 Replies

Hi, just wondering if anyone has had painful heels especially when walking while being on Interferon? I’ve been on interferon for around 9 months and every so often I struggle to walk due to the pain, it does ease off and it happens randomly. I didn’t have this before taking interferon. I have heard that it could be due to dehydration so was just wondering if anyone else has experienced similar.

Thanks in advance 😊

Written by
beckyluck profile image
beckyluck
To view profiles and participate in discussions please or .
Read more about...
17 Replies
hunter5582 profile image
hunter5582

I have never heard of this specific issue due to the IFNs. The IFNs can cause arthralgia or myalgia but I do not think that sounds like what you are describing. Suggest you consult a MPN Specialist experienced with managing IFNs to get the best answer to your question. Meanwhile, there is no downside to improving hydration. It may not help but it certainly will not hurt.

beckyluck profile image
beckyluck in reply tohunter5582

Thank you for your response hunter5582 😊

Jamesxyz profile image
Jamesxyz

Hi,

Did you get an Xray? If so did it show anything?

beckyluck profile image
beckyluck in reply toJamesxyz

Sorry for the delay, I haven't been to the doctor's yet, I will be speaking to my consultant in the next few weeks so will see what she says.

Mazcd profile image
MazcdPartnerMPNVoice

hi beckyluck, so sorry to hear that you are experiencing pain in your heels, best to speak to your haematologist and also your GP, just to get it investigated, it may not be anything to do with the interferon or your MPN, so best to get it looked at. Best wishes, Maz

beckyluck profile image
beckyluck in reply toMazcd

Thank you Mazcd, I will be speaking to my consultant soon but am thinking of getting an appointment with the doctors anyway.

Ovidess profile image
Ovidess

I'm on Besremi and for a similar period of time. I'm also having unexpected feet problems, and assumed it was an arthritic reaction to the meds (or to --??). It feels as if my arches have fallen, or as if I no longer have a spring in my step, so that I seem to be pounding the pavement instead of walking. I'm taking hyaluronic acid with MSM as a supplement, and am playing a wait and see game, hoping I'm experiencing some weird seasonal joint crankiness. My next doctor appointment is in April.

beckyluck profile image
beckyluck in reply toOvidess

I hope you get some answers when you see your doctor this month. My pain is just on my heels when I walk, I also have really tight calves.

Mufftreacs profile image
Mufftreacs

pain in heels.

Hi,

I was on Peg interferon for some time and tried everything that might help my painful heels. My podiatrist was at loss.

Quite by chance, I had to change to Rux as my ET progressed to MF. In approx one week, the pain had disappeared. My MPN consultant was quite surprised as she did not think painful heels could be connected to Peg. However, I think it is a side effect of Peg but quite a rare one. I had painful feet for well over a year and at times walked with a stick. After changing to Rux the problem simply went away. I think my consultant was most interested and made a note of it.

Hope this helps.

Katie

EPguy profile image
EPguy in reply toMufftreacs

Could be a pattern showing in this thread, your case especially. The US FDA encourages pts to report adverse events, esp ones not on the label. Other countries likely have something similar.

beckyluck profile image
beckyluck in reply toMufftreacs

Hi Katie,

When I mentioned it to my consultant she said that she hadn't heard of this side effect, it started not long after I started on Peg interferon and its not changed over time, so I thought maybe it is just a coincidence? But its not going away, I don't have it all the time and I also have really tight calves, I think I will get a doctors appointment anyway just incase it is something else but will also mention what you have said to my consultant next time I see her.

Thanks Katie x

Mufftreacs profile image
Mufftreacs in reply tobeckyluck

Beckuck heels

Mufftreacs profile image
Mufftreacs in reply toMufftreacs

Hi Beckyluck,

My consultant did not think it was anything to do with peg for months and months. She said it was plantar fasciitis. However, when I had to come off peg , having progressed to MF and the pain went away almost immediately, she was interested and made a note of it.

Hope this helps.

Katie

Mortysdad profile image
Mortysdad

Hi Beckyluck, I have been on Pegasys since Nov 2022 and it was only 3 months ago I started having pain in my heels. It would get very painful to even walk on. It was mainly the right one so I just thought I must have come down hard playing racquetball and injured it. It comes and goes but is never gone for more than a few days. I was thinking possibly plantar faciitus as it follows those symptoms. I mentioned it to my Hemo a few weeks ago as she always asks if I have any bone pain, but when I said heels, I could see no lights went on. Keep us posted though as maybe there's something here. All the best!

beckyluck profile image
beckyluck in reply toMortysdad

Hi Mortysdad, yours sounds just like mine, I will keep you posted as and when I get any more info. Thanks

gilded profile image
gilded

Hi beckyluck. I’ve been on 90mcg Peg interferon fortnightly and 1 aspirin daily for about 2 years. I have ET CALR+. Some weeks ago I developed a lump on my left heel. Putting on footwear, I was careful to avoid touching it, as it was painful. I consulted the podiatrist and he diagnosed a corn and removed it. I’m 80 years old and never, ever before have I developed corns on my heels, (only the occasional corn on my toes). Am unsure if this heel corn is connected to ET, but thought I’d mention it for what it’s worth.

beckyluck profile image
beckyluck in reply togilded

Hi gilded,

Thank you for posting, I have no lumps at all which is very frustrating, I haven't heard a connection between ET and corns before but will mention this to my consultant. I hope you do not develop any more. x

Not what you're looking for?

You may also like...

Interferon or not???

HI all, Im ET triple neg 2 years diagnosed. I initially tried Anagrelide but suffered side effects...
SuET2017 profile image

Ruxolitinib or Interferon

Hi everyone I have PV diagnosed late last year and since then it's been a bit of a roller coaster...

Anyone on Interferon for 5 years or more??

I just read a post of a member who has been on Peg for 5 years and has an AB of 1%. Wondering...
Meatloaf9 profile image

Pain in legs

Hi Guys, I was just wondering if anyone else suffers from a really uncomfortable dull aching pain...

Unbearable night cramps in legs/bone pain after upping interferon - related?

Hi everyone, I'm new here. I started on 90mcg of Peg. Interferon a month ago. No side effects. Last...

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.