Deanna's Journey - This Love Is Forever

Deanna's Journey - This Love Is Forever Help Deanna in her fight against Lymphoma. Beyond all of time, this love is a forever love... Deanna's journey begins.... Special creams would make me itch more.

Help Deanna in her fight against Lymphoma

Beyond all of time, this love is a forever love... Deanna's journey begins....

Being unwell for over a year, and now recently being diagnosed with Lymphoma Cancer, Deanna sets off on her fight to beat cancer.. For those of you who don't know me but have chosen to follow this page and offer your support here is my background story of how I came to be where I am now. I am Deanna Johnston a 42 year old, self employed travel broker, living in Whangarei with my partner and our two gorgeous young children. I have been itching for months and months. I have been so uncomfortable, to the point where I felt close to mentalism (often telling my dermatologist that I am nearing being in a straight jacket because I cannot take much more of the terrible itching. I first went to Doctor in December of last year after approximately 3 months as my itching got so bad. I was going Insane for first of multiple times. My normal Doctor was not on so I had to see a Locum who hardly took notice of what I was saying and said I had Scabies. I replied that this wasn't the case as my children would have it and that I had been this way for a few months. But despite this I was treated for Scabies 3 times. Nothing changed and I continued to itch. I went back and saw my Doctor who put me on creams, antihistamines and more. And I was then referred to a dermatologist. My Body was covered in sores from scratching. People would tell me to stop but I couldn't it was unbearable. I would constantly be trying alternatives like Baking Soda and Vinegar to name just a couple (I was Googling alternatives desperate for ideas or something that would give me relief). Some things would help temporarily but nothing gave long term relief. By the time I saw the Dermatologist, his prognosis was insect bites, fleas, bed bugs which I seriously doubted as this was starting to affecting me from Head to Toe. No one else in the family was getting bitten. But listening to the Doctor the Dog was fleaed regularly and house flea bombed for good measure but as I thought would be the case I continued to itch. I was only seeing dermatologist every six weeks and at one stage when I saw him my sores seemed a lot better with more creams and antibiotics and antihistamines, steroids but I was still itching. Then it got so bad even Dermatologist got a shock when he saw my entire body covered in sores. I would ring him in-between my appointments in absolute distress and would up different steroids and changes of medication. I kept saying nothing was working and steroids were just making me mad so I stopped them. I told him I had chills, that felt like things moving under my skin it was a terrible feeling. (Later the Doctor in Hospital asked me if I had this - yet it didn't set off any warning bells with my Dermatologist) my feet were raw, my scalp felt like I had Head Lice. For over a year I have been scratching every day / all night often awake for hours with cold flannels until it eases or I finally fall back to sleep. One weekend I was so bad, I had been going downhill for a couple of weeks and between my Sister and my partner Ian they decided I needed to go to A & E. I was put on antibiotics which worked a treat and then they rang a Dermatologist at Auckland Hospital who agreed to see me so I went there next day for tests, creams, body wraps to help my skin. I was still itching but all the tests were coming back ok. They did send me for a chest xray but I didn't think there would be anything on it, so I was released to continue creams etc and see my dermatologist at normal appointment which was in a week so good timing for a follow up. They were baffled. I saw my Dermatologist the following week and he said they were still waiting for someone to get back to them on final report chest xray. They even asked if I was “open to talking to someone” which to me implied that they thought I was going mad, and I started thinking that they thought it was all in my head. I told him sure but I don't just scratch for sake of it. Here I am hiding my arms and legs as it looks like I am on P - I knew this wasn't something that I was imagining. After all this he rang me the next day saying the Xray shows shadow and they think this warrants a CT Scan so I was referred to have this done. After chasing him and the Hospital I finally got an appointment. The hospital then rang to tell me the CT Scan was broken so we changed plans and headed to Northland Radiology (who by the way were great). My scan was at 11.30am. The Dermatologist rang me at 3.30pm saying they found the reason for my itching and that I had Lymphoma. I was at home alone with my two small children Thomas and Hannah. I rang Ian and family who came running it was a massive shock to us all. The next step was heading straight to Whangarei Hospital to talk to Doctor. The Doctors and Nurses at Whangarei Hospital have been fantastic. I had more blood tests, a bone marrow biopsy, a needle biopsy through chest and was given drugs to help my cough (which by the way is something else I have had ongoing issues with over previous month and is now back). The Bone Marrow came back clear which was such a huge relief, however the needle biopsy was inconclusive. This is my Story as briefly as I can explain leading up to where we are now and when we began this page which is providing me so much love and support. You will have read the recent posts explain where we are at now but for those who are new our next step is now to have the major operation to access the mass behind my lung for a second biopsy which will take place next Wednesday from there we will hopefully have a much clearer picture of treatments and where too next. Again I thank everyone who has so kindly ‘liked’ this page I read everyone’s comments and am truly overwhelmed by all your kind words. I will keep you posted as I continue on my journey.

**5 YEARS!** I was so sick this day. Funny doesn't look like it in the picture but I could not have cake and could not s...
12/05/2020

**5 YEARS!** I was so sick this day. Funny doesn't look like it in the picture but I could not have cake and could not stop being sick!! Life sure does fly by. To all the those with Cancer, keep strong and focus, you an do this!!!

Deanna Johnston
13 May 2015 ·
Hurrah!!! Last Chemo today. Big Thank you sis - Kerry Ginders for making awesome cake and to the nurses at Cancer Centre for looking after me the last few months. Special thanks to Jodi and to Sue and Brenda (Unfortunately MIA today) and to all those throughout who have helped With the kids, support, baking, cooking all those who helped us financially, my kids and to you all for following my page and your lovely words and kindness!!

29/04/2019

Spent a lovely day with my beautiful sister having her 2nd to last chemo session. Just one more to go yipee

It's been 3 years since my last Chemo. In many respects this is fantastic, and a testament to improved diagnosis and tre...
12/05/2018

It's been 3 years since my last Chemo.
In many respects this is fantastic, and a testament to improved diagnosis and treatment options. But survivorship for me came at a psychological and physical price.
In some ways, the ongoing psychological and emotional challenges I have faced have been worse than the physical treatments I endured.
I became emotionally paralyzed - I switched off from love and found it hard to make major decisions, to care, I turned off from friends and family and I feared and still fear recurrence even though I know anything can hit us at anytime. I found it hard to be a Mum and that's the hardest Job at the best of times!
Anxiety and Fear are huge! You feel still feel guilty that you survived and others didn't.

- Losing Mum so suddenly which hurts everyday proved that life is short, the last 3 years have been hard and last 6 months even harder as I try to come out the other side. For some reason surviving is worse than getting sick and dying.
Although happy to be alive, and watch my kids grow, the emotional flow has not been easy.
When Life Gets hard, It makes you Stronger but remember to live! XO

"Life is too short to wake up with regrets. Love the people who treat you right, Forget about the ones who don’t. Believ...
13/11/2017

"Life is too short to wake up with regrets. Love the people who treat you right, Forget about the ones who don’t. Believe everything happens for a reason.
If you get a second chance, grab it with both hands. If it changes your life, let it. Nobody said life would be easy. They just promised it would be worth it." -― Harvey MacKay

Wow!  To think in May it would be 2 years since my last chemo!  I have been given the clear by the Specialist!!  No more...
07/03/2017

Wow! To think in May it would be 2 years since my last chemo! I have been given the clear by the Specialist!! No more visits!! To think this was me 2 years ago and now!! Staying strong and positive and having 2 young children certainly got me through. Sometimes we don't have a choice and have to deal with what is thrown at us! Take Care xo

Maybe this time!!  High chance may be cancelled again. Heres hoping not.
22/04/2016

Maybe this time!! High chance may be cancelled again. Heres hoping not.

Early Start, last on morning list - 2 hours later out Surgery Cancelled due to Acute cases last night coming in. I under...
14/04/2016

Early Start, last on morning list - 2 hours later out Surgery Cancelled due to Acute cases last night coming in. I understand people more Urgent but phoning first thing this morning or last night would of been good idea!!

Yippee!!  All scheduled for Surgery for Friday. FINALLY have my portacath (port) out.  I Will have a general anesthetic ...
11/04/2016

Yippee!! All scheduled for Surgery for Friday.
FINALLY have my portacath (port) out.
I Will have a general anesthetic and need to be at the Hospital bright and early. My port was supposed to be flushed every month but this has not happened so would hate to see what state its going to be in for them to take out. I had a chest x-ray a couple of weeks back and my specialist did not realize it was still in. I did ring the Hospital but they wanted it in for around 6 months after chemo (I should have kept ringing them-life just gets so busy)
My kids always say "Mummy we can't touch that side eh" Now they will be happy to punch me on both sides!! hahaha kids!!

Woah!  1st time in about 2 years. Made it. Now for the run down - easy part.
27/02/2016

Woah! 1st time in about 2 years. Made it. Now for the run down - easy part.

Wow! its been 1 year ago, today, when I first received Chemothreapy. Amazing what a year does!  This is me today!
08/12/2015

Wow! its been 1 year ago, today, when I first received Chemothreapy. Amazing what a year does! This is me today!

Well it was about a year ago today that I was told I had Cancer.  It took another gruelling 7 weeks, a lot of tests, a c...
15/10/2015

Well it was about a year ago today that I was told I had Cancer. It took another gruelling 7 weeks, a lot of tests, a couple of scans, a couple of operations and a lot of patience! We had to learn exactly what it was, how to treat it and where to treat it.
It was all a bit of a blur, looking back and apart from the niggles and the short hair seems a long time ago. Yet I am only 5 months post chemo to date!
I had another cortisone injection in my wrist on Tuesday as this had worn off. My Wrist still has not healed from where I had a Central line in, from Surgery in Auckland.
My hair is growing back! Yet to determine a style haha.
I still have my port in and am due for a check up with the Specialist but all looking rosy.

Tessa had exactly what I had.  Sad that both her and her Dad suffered together but also great at same time, to have some...
17/08/2015

Tessa had exactly what I had. Sad that both her and her Dad suffered together but also great at same time, to have someone so close understand what she was going through.

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