Just diagnosed with Heberdens Nodes / Osteoarthritis, received no help/support, help please?
Posted , 10 users are following.
After having pain in finger joints, swelling, lumps and red / warm to touch, I went the doctors yesterday and after a very brief 5 min appointment was told I had osteoarthritis / Heberden's nodes. I was really upset as i am only 46 and a childminder, so constantly doing up buckles on car seats, buggies, high chairs etc and also have 4 children and a young daughter. I managed to ask if I could take anything to help and slow down process as within a couple of months the lumps have grown rapidly on 3 fingers on left hand and look like starting on right. He just said well you could gtry glucosomine if you want some doctors think it does nothing some doctors think it helps, up to you!!! I am absolutely devastated as I have no idea how this will affect me in the future. Any advice / knowledge would be extremely appreciated. Thank you so much.
2 likes, 13 replies
catsmother tillymint62
Posted
I completely understand your frustration and how upset you
feel !! I've had the same kind of answers from some Doctors over the years! They DO NOT understand how OA affects those of us that are afflicted with this chronic debilitating illness!
I don't have much luck with mefication I'm afraid, so, sorry I can't advise you on that, but, I know there will be someone on this site who will be able to.
I would suggest if it's possible, change your GP!! There ARE some who try gpgo help us, after all, they ARE there to help us!
that's what they're paid to do!
Try to get a other GP to hear and see how bad you are, it just
isnt right that we should struggle to be heard, especially by
someone who's job it is to listen and to help!
YoyYou have every right to ask to see anoyanother Gp on the
practice if there are any.
What a dreadful situation to be in.
My thoughts and prayers are with you.
Please keep us informed, and just remember, there are lots and
lots of us on here who will be rooting for you!
Take care,
Love,
catsmother..xx
catsmother tillymint62
Posted
catsmother tillymint62
Posted
madeleine94884 tillymint62
Posted
I too have had bad experiences with one of my GP's - after getting an x-ray which showed severe OA in my neck, my GP told me "get on with it, nothing can be done". I paid for a second opinion, he was talking rubbish, I was offered an operation which has been a life saver. I've also had operations on my fingers, mainly successful, though not always. Please don't despair, there are some doctors out there who ARE able to help.
Madeleine.
bozzer madeleine94884
Posted
madeleine94884 tillymint62
Posted
bozzer madeleine94884
Posted
catsmother madeleine94884
Posted
have to put up with it! Keep well.
Xx
loxie tillymint62
Posted
karen08277 tillymint62
Posted
I also suffer from heberdes and bouchards OA you need to go back to your GP and ask to be refered to an occupational therapist,i was diagnosed in 2012 but started with it a few years earlier,i wear a thumb support on both hands and a finger splint they are very helpfull as they restrict movement,i am in the process of having another set made,but unfortunately i am now having to give up work as i am a domestic in a nursing home and the work is very demanding and i can no longer cope.i hope this has helped a little
regards karen.
noorhudah karen08277
Posted
Hi Karen,
I know this is an old post, I was recently diagnosed with OA for my knees and noticed the nodes resembling Heberden's on 2 of my fingers. I did highlighted my Orthopaedic but he simply said to just leave it. I find it really worrying if it will worsen. I am 43 years old and am a mother of 4. I cannot imagine what my life will be if I can't use my hands. How are you getting on, 7 years since your last post? I am from Singapore.
wknight tillymint62
Posted
I trust my consultant as I think he has been very honest with me and when he can make a difference he does, two finger joint replacments later, we joke about what will be the next think he will fix on my hand and I know it wont be the nodes.
barbara66703 tillymint62
Posted
I have read but not tried this but researchers found that low-level laser therapy reduced pain and swelling and increased mobility in people with Heberden’s and Bouchard’s nodes. i also had node treated by a had specialist.
Try acupuncture treatment and paraffin wax which is a type of heat therapy. I use lavender scented wax and in hand foot sauna that melts wax to comfortable temp. Then dip hands in warm wax 2-3 times for warmer treatment. Allow to cool on hand then remove wax. rest has quietly for 10-15 minutes.
Also I wear special gloves at night and special gloves during the day that are designed for hand pain, some gloves also can be warmed in a microwave , feels so relaxing, calming and melts the pain away.
Soaking hands in a solution of warm water and magnesium salts or taking magnesium helps.
Just a simple wrapping a warm towel (warmed in the microwave or in warm water) around your hand is helpful.
Next is to see a hand specialist.