I know there was a discussion a long while back about coloring our hair. Are any of you coloring? Gray is driving me crazy🙃
Gail 🦋
I know there was a discussion a long while back about coloring our hair. Are any of you coloring? Gray is driving me crazy🙃
Gail 🦋
I’ve been colouring my hair for 30 years
I have been diagnosed with pbc 10 years
I’m not ready to stop yet
I’ve read the conjecture but there is no proof the colouring your hair is a factor for triggering pbc as far as I know
I highlight mine well what is left of it. With foils the product does not touch the skin so I am told. 😊
Hi I colour my hair have done for some years. It would really get me down if I didn't. We must still live our lives and be happy and if that means getting rid of the greys do it. 😀
Just to be on the safe side I have foils to highlight my hair. My hairdresser does her best so that no dye is touching my scalp.
Hi l have foils so the colour doesn’t touch my scalp I have lots of grey hair as well. I used to have a full head colour at the hairdressers but for some reason l became allergic to all the products and my scalp started to burn and itch so now my hairdresser uses foils which l love. I personally would not buy products off the shelf and colour it myself
I let my hair grow out when I was diagnosed with PBC, however, my hair is completely gray now. I have done so much research on this particular issue. I believe the reason we are not supposed to color our hair is our liver struggles to filter out the poison which gets soaked into our scalp. I did find a product called “Naturtint” sold through Amazon, which is supposed to be ALL natural ingredients. I have not tried it yet, but I am going to. I already ordered it.
Go for it!
Yes I still colour and will do until I’m ready to go all grey- for a change of style not because of pbc. My hairdresser gets in a healthier more natural dye - ask your hairdresser to research product for you.
Some time back one of the ladies had an appointment at the May Clinic. She asked them about coloring her hair and they said it was okay. Personally, I have let my hair go more because my hair was getting fried and it was so expensive. I've been trying to save a little here and there because retirement is coming up soon. I got lucky, people say it looks good. If it didn't I would probably start coloring it again. I noticed it didn't really make any difference on my lft's. This disease does enough to us in an emotional way. You can't go around feeling like you don't look good.
Pam
4pjx...my gray doesn’t really make me feel bad about myself. I have a little more gray at the front but all else blends nicely. My gray is soft & I have blue eyes so not that bad. I try to keep a nice cut which helps. There’s just something about gray hair on a pink scalp 😆
I did stop using nail polish as it makes little difference to my appearance. However when i tried going grey, it was not a nice grey and put about 10 years on me. So I decided to continue colouring. I reasoned it is an unproven theory anyway ☺☺
I do it myself with Nice and Easy about every two months. My labs reduced when I went on urso about 5 years ago and have stayed down. There are 4 people in my family with PBC so I think it's genetic
Me too ☺
For about 25 years I coloured my hair myself at home, using Nice and Easy , or Garnier. diagnosed with pbc 2 years ago and found the colour was just not holding. Rather than colouring every three weeks I've decided to flag it. I started a new job so it was a new start new look and my hair is white.
I think it looks ok One of my friends that hadn't seen me for a while complimented me and asked me how and where I got my hair done, so I laughed and told her it's actually undone.
Lol. Bonus
I use colour named Elumen - they say it is healthier than other colours. Perhaps...
Still colour mine at home, but If the theory of hair dye, nail varnish or cosmetics ever becoming the cause then I would stop. My own theroy is this, I am of 10, all the girls 5, use all the products I’am the only one with PBC. No other family members now or past have had it diagnosed either. So I’am a wait and see... we breathe in chemicals every day in our environment, I worked in a petroleum station many years ago was that petrol the trigger we breathe it when we fill our cars so I’am not going to panic over haute dye yet.
Candy12... I never thought it caused PBC, I just didn’t know if the chemicals were too hard on the liver. Thanks so much😊
I had never coloured my hair when I first got pbc... X
As your question is "any of you colouring?" I have to say - no, I don't colour my white/gray hair but may I ask you, are you sure it is the gray that's driving you crazy? May you just want to make a radical reaction to a change that you didn't choose? That may be the first question to ask yourself. It could save you money and time? You are perfect as you are. If you decide to color, that will be fine too. It is lovely to be free to choose? Your hair looked lovely in your Christmas good wishes pic here. I'm sure it always will look beautiful whatever you choose. My hep inferred that people who had longtime been dying hair is a group that seems to have higher incidence of PBC. I have never searched or seen any evidence of that. Seems likely to me that since most women are diagnosed when they would naturally be gray, and most women colour gray hair, that they would be the group most likely to have PBC!!
I have always coloured my hair as not yet ready to go grey. My consultant has not suggested that I should stop using hair colour so will continue to do so.
I do....not ready to give that up! I feel like it’s the only thing keeping me even slightly young looking. 😉
I was diagnosed 6 years ago and have always colored my hair, no problems with doing it.
I actually have it done at a salon and I have my nails done probably 2x a month. I’m a pediatric nurse, I work 4 10 hr days. I am 60 years old,
Good for you, I think keeping busy helps. Take care of yourself!