Click on Link...  for a old Home Feeling...

http://www.leukemia-lymphoma.org/ubb.adp?frame_url=http://ubb-lls.leukemia-lymphoma.org/cgi-bin/ubbcgi/Ultimate.cgi?action=intro&item_id=9388

Yes...  it starting to feel like Home now... 

CLL  and   SLL  just  kissing cousins...

Good Luck..   Happy Spring Time..

Greetings.

One of my favorite color link that really help me understand more

about some of the treatment drugs and make them seem not so scary

click link below..   Good Luck .

http://www.healthvalue.net/actionantiCD20engl.html

Keep sharing and posting your experience and updates.  It really does help

so many.

Greetings

I was looking at this website.  Just brushing up my understanding a little how things work with some treatments Interesting..

click on link below  ...      Keep posting and sharing updates..  comparing notes. and experiences help everyone.. Good Luck

http://www.healthvalue.net/actionantiCD20engl.html

Thanks for reading and sharing your experience

It is almost the middle of July now. I am still holding my own. Even with CLL.  my nodes have been the issus more.  From feeling my neck nodes

for years now.  I know the nodes swell and shrink with different  things that happen with my body.  Rest is one key good thing.  Sinus issue can

cause nodes to swell.   Keep moving by working or active.. seem to help keep the blood flowing and I feel help my nodes stay more normal.

The herbs and finding that balance or vitamins herbs, eating food. Also drinking water.. Balance seem to be the key for me.

If you google  Rosy Periwinkle Flower.  you maybe like me and  find this plant very interesting.  They use it for cancer drugs, and it has a lot of

other anti-cancer elements as well.   I fund this by doing some gardening at home.  What a interesting plant.. and I having a blood cancer.

Some things are just fate.   I still hanging in there.  I think I will make for 9 months with out seeing or visiting a clinic or hospital.. this will be a record.

good luck

http://www.healthvalue.net/actionantiCD20engl.html

Ascen

Oh yes.. I lurk here and there...  Over 8 years now.. heading for 9...years...wow..  I would have never thought it..

You had a transplant.. interesting..   can you share something about the experience..  do you take any extra drugs now.. ??  are you back pretty good?

a friend of mine is going  thru one now..  about  3 weeks post  blood test look pretty good ,  had to start taking some extra pills to smooth out

rejection issues...  over all  it was out patient so far.. the mask and being careful and resting.. diet changes...etc..

any tips.. for us , the in and outs to a smooth transplant..  thanks for posting a note..

I like the old board but change is what seem to happen,  I sure have no control...  take care