Blood clot disorders: How does this affect your quality of life?
I have 3 blood clot disorders is that common? I have not seen a Dr since right when covid started or been on medication.How will that affect my life quality
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
I once approached my GP about treating symptoms, which is the medical tactic, and not treating the disease; his response was that often times, all that there is to go on are the symptoms: therefore treat them (the symptoms) the best as you are able.
Hugs back to the 2 of you and thanks.
Susan
Hello I saw your comment and wanted to reply. I’m 57 and have PolycythemiaVera. I’m in full flown menopause. The tingling and aches and hot flashes are crazy and constant. I was told from my oncologist NO HORMONES. So I tried non prescription things they recommended but they didn’t work. Blood clots are a serious concern. I wanted to let you know I was prescribed Clonidine for the hot flashes and it has made a huge difference. This is kind of off topic but I thought I’d share. It’s a blood pressure med that’s been around forever and super cheap. I don’t have high BP and it only lowered it by 10 points or so. I take .1 mg twice a day. You can Google it. I wish you luck with your illness and this change too!
Thanks! I will ask him about hyaloronic acid gel injections.
I had a CT scan for the possibility of follicular lymphoma, which was positive by biopsy. But in the CT scan they saw multiple small blood clots in my lungs. That very evening I was started on blood thinners. I have no symptoms. I understand with lymphoma cancers, that blood clots are a possibility.
Welcome to Connect, @loislillypadd. It was fortunate that your doctors discovered the small blood clots in your lungs in time to treat them. That revelation had to a bit frightening for you, I’m sure! Did the scan also show any other lymph node involvement with your follicular lymphoma besides the node that was biopsied?
We have a number of members in Connect who also have Follicular Lymphoma. If you haven’t seen some of the posts already, I’d like to introduce you to @traceyt @caracello22 @puddknocker and many others who have FL and share their experiences in this discussion:
>Follicular Lymphoma: looking to connect with others.
https://connect.mayoclinic.org/discussion/follicular-lymphoma-at-age-44/
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Another discussion was started with @valandsheri when Val required treatment for his Follicular Lymphoma. Here is that post:
~Starting Bendamustine and Rituxin for Follicular Lymphoma
https://connect.mayoclinic.org/discussion/starting-bendamustine-and-rituxin-for-follicular-lymphoma/
Follicular Lymphoma is generally slow to develop and in early stages often doesn’t require any treatment. How long ago was your diagnosis? Are you in the ‘active surveillance’ period or are you in treatment besides being on blood thinners?
This is my 3rd adventure with cancer. 2009 it was thyroid cancer. 2020 it was breast cancer, and then this pass fall i palpated enlarged lymph nodes in my left groin. This was confirmed by biopsy to be a follicular lymphoma in my left groin and also in my right axillary area. An earlier CT scan picked up on numerous small blood clots in my lungs.
A point of interest is that my husband died October 20, 2023 and I got a sure diagnosis 10 days later of the follicular lymphoma.
I thank you for your interest, and I’m sure this feed will be supportive and enlightening.
I am in treatment, for it was advised at 75 years of age It is better to do my treatment at my present state of health rather than surveillance. I have had five treatments thus far with her BENDEKA, & RITUXAN. I have three more treatments yet to go.
I appreciate the contact information you’ve given me and will surely follow up. Lois
Thank you for your hugs.