Thank you a lot for sharing.
3 years post bone marrow transplant, and my hair probably was still rather short, think and has bald spots.
It’s virtually big to understand that others have experienced what we have gone and am currently going through. Besides, the journey to ‘selfacceptance’ in the post treatment body was always sophisticated. You see, my doctors ld me they not sure if bald spots will ever go away because of most of chemo therapy. On p of this, kudos to you for writing this article. Insecurities of weight and natural appearance are always a massive issue for junior adults that impact people’s lives in confident and health threatening ways. Of course so rather often we’re ld the simply be grateful to be alive! A well-reputed fact that was probably. Almost any single day, I actually am grateful.
I see I am not alone in this.
Although it improves with every inch of hair regrowth, my ‘selfesteem’ after cancer, was horrible after watching my body drastically revisal in this rather short time.
Yes, I am grateful to be alive. Cancer survivors are not exempt from these insecurities. On p of that, if our treatment has made them worse or created insecurities that under no circumstances, till today, therefore this needs to be addressed. Telling survivors that they should simply be thankful for the bigger picture, completely negates the lower stark reality ‘self esteem’ problems that will strike most confident of us after a battle of cancer. For instance, I usually felt stupid for lamenting my hair so constantly. Bald is beautiful,with no doubt I know it’s. This is case. For a few of us, we under no circumstances felt beautiful as bald. So, we used to just sit and stare at pictures of my hair before they lost it, when my hair was growing back.
That voice needs to be in the conversation intending to make a long time until it’s that long once more.
I was alive, after all. They would like to ask you something. What’s hair in survival bigger picture? That it isokayto not feel beautiful while bald. Nonetheless, it’s a real mourning process, one that I am merely now eventually get used to accept over a year later as my hair has reached a length I am eventually comfortable with. Eyebrows and eyelashes were usually more challenging to replicate but a wig was simply soaccessible. It was treatment one aspect we could control to at least look as normal as they wanted to feel. All the time they wore my wigs to my chemo sessions at the clinic and possibly I’d make them off during infusions but they’d oftentimes go back on for selfies or when they will have travellers.
Despite how uncomfortable and miserable those wigs were, I’m pretty sure I would wear them virtually on a regular basis.
Nearly any time we left the house, I would wear that wig.
On weeks I felt like hell in a hand basket traveling down a stream of chemical misery, I would put that wig on. Thankfully, To be honest I started offobsessing over when my hair would grow back, when I hit remission. It humbled me to see others with worse cancers than mine and reminded me of how lucky I am. When my hair was a stubby GI Jane cut, is all about when they began meeting another cancer survivors. In bigger picture, it’s simply hair. Now looking back on it, I reckon it was a combination of one and the other. Oftentimes I cried that day.
Possibly part of it was how I viewed my cancer as aweakness that some will exploit.
I was simply not comfortable being seen as sick cancer girl.
It was virtually as terrible as the day we was diagnosed with cancer. Like so most of us, I’ll under no circumstances lose, absolute utter devastation I felt when those first few strands of hair dropped out. Probably part of it was wrapped up in my loss vanity that I had for my hair. Whenever losing my core natural identity, shattered my reality, mething about losing my hair. Now pay attention please. I didn’t cry day they was diagnosed. Mental health could be so connected to problems of special appearance that Surely it’s insane to not address how this impacts cancer survivors, particularly green adults, that have simply experienced sudden and drastic improvements to their body that they should be struggling to accept.
Whenever losing that piece of yourself usually can be devastating, hair is this particular core identity marker and for survivors like me.
It’s something that for so a lot of us happened to be an uphill battle of self acceptance.
It’sokay to feel that way. Even if I’ve always written onthisduring treatment, it’s so crucial that here I am talking about it,. It was a crucial part to my physic identity. With that said, I curled it, colored it, primped it, fluffed it. That’s right! My hair was a massive part of my identity before we was diagnosed with ‘nonHodgkin”s lymphoma in February they have, for lots of years of my existence, often been a woman that cared a huge bit about my hair.