Rolling veins
Comments
-
Hi, mum had her first treatment and I felt so sorry for her. She is totally needle fobick and as if your not nervous enough it took 3 nurses to find a vein, which is painful and she seemed to have rolling veins. She was fainting, crying, not a good start...!!
Day 2 and she started feeling fluey and had a very red face, reaction to anti sick drugs, anyone eles had that?
Silly question but how long dose feeling rough last after chemo? Mums hoping only for 3 days and then she thinks she will feel better, I dont know where she has got this time scale in her head.
-
-
I am also needle phobic and have horrible thin, tiny, rolling veins. I had a port put in for chemo therapy and blood sampling and am very glad I did. I second the idea of your Mom checking into having a port put in.
I also had problems with my anti nausea drugs. Side effects included blurred vision, headache, and the jitters. The SEs were better, however, than heaving my guts out.
I found that I usually started to feel better by the fourth day after chemo. I had AC, your Mom's drugs may be different.
-
I have had 2 treatments so far. My cocktail is called FEC. I seemed to have gotten every side effect mentioned - but the actual treatment its self went ok.
For the second treatment - when they put in the E - I call it the "Evil one" its red - my hand and forearm started to feel tight. The nurse would pull it back and push it in to check blood flow. Being an accountant I don't understand the significance of any of these words. Well a week later - being back to the clinic for them to check my arm and then to ER as I woke up with my hand totally swollen - nurse said put hot compresses - doctor said put on cold compresses - its still swollen. My vein in the crook of my arm they can't get a needle in. I wanted to hold off putting in a port in because we are going vacationing in BC and I want to go swimming. They said it can't be submerged. It's day 8 after treatment and starting to get energy back but in little bits - 6 more treatments to go. This isnt as easy as some people told me it would be but I guess it is what it is. Has anyone else had this issue with their arm? I am not sure whether to be alarmed or just put it down to just another invasion of my body?
-
Sue, I am an ER nurse and wish I was there to help you with your veins. Medications make veins weak but there are some veins better than others. It has always annoyed me to see nurses go for hand veins and inner elbow veins. The patient has to leave their arm straight, hand straight etc.
Some tips to give the person inserting an IV.
If one tourniquet works good, 2-4 work better. This is often needed for larger arms or dark skin.
As for veins, if you follow the outside edge of your thumb, along the wrist where it bends, there is a nice big vein that allows you to bend your wrist even with an IV. The big great vein is along the under-outside edge of the wrist forearm. If you sit with your elbow bent fist up toward chin and feel with your fingers (opposite hand) along this area over the forearm muscle, you should feel a nice vein. Again, it is protected by a stable bone so bending your arm is not a problem. Try to palpate these veins yourself and show them to your "sticker".. Good Luck..Jaq
-
Hi Merlin, Oh, your poor mom. I am exactly the same way with needles! I had four AC treatments without a port. To be honest, every time I sat down in the chemo chair, I cried. I can't say why either, possibly fear, nerves, dread, etc. Once the Ativan kicked in, I usually just fell asleep (but I did stop crying). Anyway, I had my chemo on Wednesdays. I usually felt okay for Wed and Thurs and then felt tired and sickly Fri and Sat and would feel pretty good by Monday (would go back to work until next chemo treatment). I think the red face your mother is experiencing could be from steroids given before the chemo. I had that too. The "fluey" feeling is just the normal post-chemo feeling. What helped me was sleeping it off the third and fourth days. I hope your mom's next treatment went better for her. It is so hard and so scary....I completely understand.
Missjaq, Thank you so very, very much for the vein information. I found it and your are right...it is a great big, wonderful vein! I just had bloodwork five days ago. The nurse who always does my blood draws and, up until that day only needed one stick, had to stick me twice and had a very hard time getting blood (even with the butterfly or little kid's needle). Needless to say, the inside of my only "good" arm is completely black and blue just from those two sticks. I have to go for a bone scan tomorrow, and I am going to show them my new-found vein! Thanks so very much!
Bless you both,
Cheryl
-
Cheryl could you or anyone give me some reasurance about my mums back ache!! you know what we are both worried about that the cancer has gone into her bones, so scared.
-
Hi Sharon,
I have had upper back pain for a few months now. I was literally trying to just ignore it because it had me so scared (which I know is a bad thing to do). I am just over two years out from diagnosis, and my coping mechanisms for anything are just gone. So, I have found that sticking my head in the sand, so to speak, is the only way I can face each day. I just had another 6-month checkup with my onc and mentioned the pain, and this is the reason I had to have a bone scan. Now I am waiting and just making myself crazy with worry.
I wish I could offer something to calm you and your mom. Unfortunately, I think the "fear" is the new normal for us. Can she ask her oncologist for a bone scan or MRI to see if there is anything going on? Is she still in treatment? I only had chemo (no radiation), and shortly after my last infusion, my onc ordered a repeat abdominal CT scan to check a spot on my liver that I had before chemo. It was determined that it was a cyst. Has your mom mentioned her backache to her doctor?
I can only say that even one and a half years out of treatment, I am physically not the person that I was before. I have many aches and pains, fatigue easily, and emotionally feel drained. I would ask your mom's doctor for a scan. It is probably "just a backache", but it would ease your mom's worry and let her concentrate on getting better. I know for a lot of us every little ache and pain is troubling and most times turns out to just be something "normal". I hope that you and your mom can get some answers from her doctor and that she is on her way to healing.
Bless you both!
Cheryl
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team